Skip to main content
Advertisement
Browse Subject Areas
?

Click through the PLOS taxonomy to find articles in your field.

For more information about PLOS Subject Areas, click here.

  • Loading metrics

Effectiveness of elastic therapeutic taping in pain management after median sternotomy: A randomized controlled trial

  • Alp Özel ,

    Roles Conceptualization, Data curation, Funding acquisition, Investigation, Methodology, Project administration, Supervision, Writing – original draft, Writing – review & editing

    alpozel@ibu.edu.tr

    Affiliation Department of Physiotherapy and Rehabilitation, Faculty of Health Sciences, Bolu Abant Izzet Baysal University, Bolu, Turkey

    ⨯
  • Umut Ata Uğraş,

    Roles Conceptualization, Data curation, Investigation, Writing – original draft, Writing – review & editing

    Affiliation Department of Cardiovascular Surgery, Faculty of Medicine, Bolu Abant Izzet Baysal University, Bolu, Turkey

    ⨯
  • Muhammet Fatih Uysal,

    Roles Conceptualization, Data curation, Formal analysis, Investigation, Methodology, Writing – original draft, Writing – review & editing

    Affiliation Department of Physiotherapy and Rehabilitation, Faculty of Health Sciences, Bolu Abant Izzet Baysal University, Bolu, Turkey

    ⨯
  • Erhan Renan Uçaroğlu

    Roles Conceptualization, Investigation, Resources, Supervision, Writing – original draft, Writing – review & editing

    Affiliation Department of Cardiovascular Surgery, Faculty of Medicine, Bolu Abant Izzet Baysal University, Bolu, Turkey

    ⨯

Abstract

To evaluate the effectiveness of elastic therapeutic taping on postoperative pain, functional mobility, sleep quality, analgesic consumption, and length of hospital stay in patients undergoing coronary artery bypass grafting (CABG) via median sternotomy. In this prospective, randomized, double-blind, placebo- and sham-controlled trial, 195 patients undergoing elective CABG were randomly assigned to elastic therapeutic taping (n = 65), placebo taping without tension (n = 65), or sham taping to a non-related region (n = 65). Elastic therapeutic taping was applied after patients were transferred from the intensive care unit to the cardiovascular surgery ward. Pain at rest and during coughing was assessed using the Visual Analog Scale (VAS) at baseline and 12, 24, and 48 hours. Secondary outcomes were Timed Up and Go (TUG), sleep quality, total analgesic use, and length of hospital stay. Data were analyzed using a prespecified two-way mixed ANOVA with Bonferroni-adjusted post hoc comparisons for the primary pain outcome. Nonparametric secondary outcomes were analyzed using Kruskal–Wallis or Friedman tests, as appropriate. At 48 hours, resting pain was lower in the elastic therapeutic taping group (19.0 ± 10.2) than placebo taping without tension group (37.5 ± 13.7) and sham taping group (41.2 ± 16.2; p = 0.001). The observed between-group reduction in pain exceeded the reported minimal clinically important difference (MCID) of 9.9 mm for acute postoperative pain, indicating a clinically meaningful treatment effect. Coughing pain was also reduced (39.2 ± 17.0 vs. 56.3 ± 17.2 and 59.4 ± 16.8; p = 0.001). Tramadol use was lower with elastic therapeutic taping (50 ± 50 mg vs. 100 ± 50 mg; p = 0.038). Elastic therapeutic taping was associated with a shorter length of hospital stay (4 [3–5] vs. 5 [4–7] days; p = 0.042). Functional mobility (TUG, p = 0.002) and sleep quality (p = 0.001) were also significantly improved in the elastic therapeutic taping group compared with the placebo and sham groups. Elastic therapeutic taping was associated with reduced pain, lower opioid use, improved early recovery, and a shorter length of hospital stay after median sternotomy.

Trial registration

ClinicalTrials.gov NCT06910215

Introduction

Despite advances in surgical and anesthetic techniques, acute postoperative pain remains a common and clinically relevant problem following coronary artery bypass grafting (CABG) via median sternotomy, affecting approximately 77–85% of patients [1]. Sternotomy-related pain delays early mobilization, impairs respiratory function, increases pulmonary complication risk, and contributes to prolonged hospitalization [2]. In addition, increased analgesic use, including opioids, can further complicate recovery by causing adverse effects such as respiratory depression, nausea, and constipation [3].

For this reason, there is increasing interest in multimodal, opioid-sparing pain management strategies after sternotomy. Elastic therapeutic taping (ETT) is a non-pharmacological intervention involving the application of elastic adhesive tape to the skin with controlled tension. It is thought to modulate pain through continuous cutaneous and proprioceptive stimulation while providing gentle biomechanical support that may reduce tissue stress during movement. Although the precise mechanisms remain uncertain, these neurophysiological and biomechanical effects have been proposed to contribute to pain reduction and improved functional recovery [4]. ETT has been shown to have beneficial effects on musculoskeletal conditions, shoulder dysfunction, and management of lymphedema [5].

Although recent studies suggest that ETT may reduce post-sternotomy pain, most have been limited by small sample sizes and single-center designs [4,6]. Moreover, in physical interventions such as taping, inadequate blinding may allow placebo and sham procedures to be distinguishable from the active treatment, increasing the risk of bias [7]. This challenge has been highlighted as a major methodological concern in non-pharmacological trials by the CONSORT statement and related guidelines [8,9].

To the best of the investigators’ knowledge, no adequately powered, double-blind randomized trial has comprehensively evaluated the opioid-sparing and functional recovery effects of sternum-targeted ETT following CABG. The aim of this randomized, double-blind, placebo- and sham-controlled trial was to evaluate the effects of ETT on pain, analgesic use, and functional recovery after CABG via median sternotomy. We hypothesized that participants receiving ETT would report lower pain scores and require less pharmacological support than those in the placebo and sham groups.

Materials and methods

Study design

This single-center, randomized, double-blind, placebo- and sham-controlled, parallel-group clinical trial evaluated the effects of ETT on postoperative pain and functional recovery after elective CABG via median sternotomy. The study was conducted at the Department of Cardiovascular Surgery, Izzet Baysal Training and Research Hospital, Bolu, Turkey. Participants were recruited between January 22 and December 24, 2025. No changes were made to the trial design, eligibility criteria, interventions, or outcome measures after trial commencement.

Randomization and blinding

Participants were randomized (1:1:1) to the ETT, placebo, or sham groups using a computer-generated block randomization sequence generated with the Blockrand package in R (v4.5.2) before participant recruitment, using fixed blocks of six participants. The randomization sequence was generated and retained by the corresponding author before participant recruitment and was not accessible to the cardiovascular surgery team responsible for participant enrollment. Eligible participants were enrolled after screening and informed consent procedures. Following enrollment, the corresponding author identified the next assignment in the pre-generated randomization sequence and communicated it to the physiotherapist responsible for tape application immediately before the intervention. Because of the nature of the intervention, the physiotherapist responsible for tape application could not be blinded, but had no role in participant enrollment, outcome assessment, or statistical analysis.

Ethical approval and informed consent

The study was approved by the Bolu Abant Izzet Baysal University Non-Interventional Clinical Research Ethics Committee (Approval No: 2025/07; Date: January 21, 2025) and conducted in accordance with the principles of the Declaration of Helsinki. Written informed consent was obtained from all participants prior to enrollment and before any study-related procedures were performed.

The trial was registered retrospectively at ClinicalTrials.gov (NCT06910215; https://clinicaltrials.gov/study/NCT06910215). Participant recruitment began on January 22, 2025, whereas the trial record was first released on March 25, 2025, and publicly posted on April 2, 2025. The delayed registration resulted from administrative procedures during trial setup. Importantly, no changes were made to the study design, eligibility criteria, interventions, outcomes, sample size calculation, or statistical analysis plan after participant enrollment began or after trial registration. The registry record reflects the original study protocol approved by the institutional ethics committee prior to recruitment. The authors confirm that all ongoing and related trials for this intervention are registered. The elastic therapeutic tapes used during the intervention were CE-certified for medical use.

Participants

A total of 238 individuals scheduled for elective CABG via median sternotomy were assessed for eligibility. Of these, 203 were randomized, and 195 were included in the final analysis. Baseline assessments were performed 6–8 hours after transfer from the intensive care unit (ICU) to the ward following clinical stabilization. Before tape application, pain at rest, pain during coughing, oxygen saturation, sleep quality, anxiety, and fatigue were assessed.

Inclusion and exclusion criteria

Male and female patients aged 18–75 years who were scheduled for elective CABG via median sternotomy, were able to understand and communicate effectively, and provided written informed consent were eligible for inclusion. Exclusion criteria were active skin disease or open wounds at the sternotomy site, known tape hypersensitivity, neurological or psychiatric disorders affecting cognition, and use of medications influencing pain perception. Additional exclusions included acute renal or hepatic failure, preoperative mechanical ventilation, planned reoperation, participation in another trial within 30 days, or revision surgery. Participant flow is presented in Fig 1.

thumbnail
Fig 1. Flow diagram of participant screening, enrollment, randomization, and follow-up.

https://doi.org/10.1371/journal.pone.0359282.g001

Interventions.

To ensure standardization, all taping procedures were performed by a certified physiotherapist with more than 10 years of experience, within 6–8 hours after the participant’s transfer to the cardiovascular surgery ward. In addition to the allocated taping intervention, all participants received the institution’s standard postoperative care following CABG. This included routine medical management, respiratory physiotherapy (diaphragmatic breathing exercises, coughing exercises, incentive spirometry, and chest percussion), early mobilization, nursing care, and standard postoperative analgesia. Postoperative care was continued until hospital discharge according to routine institutional practice. To ensure intervention fidelity, all taping procedures were performed by the same certified physiotherapist using predefined anatomical landmarks and a standardized application protocol.

Elastic therapeutic taping group.

Elastic therapeutic tape (Kinesio® Tex Gold, Kinesio Holding Corporation, USA) was applied bilaterally approximately 3 cm lateral to the sternotomy incision in a craniocaudal direction along the anterior thoracic wall. Five-centimeter tapes were applied with 25–35% tension, with the ends placed without tension and the incision avoided. All applications followed a standardized anatomical template to enhance mechanoreceptive and proprioceptive input.

Placebo taping group.

The same tape was applied to the same anatomical regions without tension and without therapeutic principles.

Sham taping group.

Tape was applied without tension to anatomically unrelated regions (scapular or paraspinal areas) to control therapist contact. All sham applications were performed by the same practitioner, using a standardized contact duration and a predefined template. All groups received the same standard postoperative analgesia protocol.

In all three groups, the tape was applied once and remained in place until completion of the 48-hour follow-up period unless early removal was required because of skin irritation or tape detachment. Representative photographs illustrating the ETT, placebo, and sham taping procedures are presented in Fig 2.

thumbnail
Fig 2. Representative photographs of the taping procedures.

(A–B) Elastic therapeutic taping (ETT). (C–D) Placebo taping (PT). (E–F) Sham taping (ST). Clinical photographs are published with written informed consent from the participants.

https://doi.org/10.1371/journal.pone.0359282.g002

Data collection and measurements

Data collection began 6–8 hours after transfer from the ICU to the ward. Pain at rest, pain during coughing, and oxygen saturation were assessed at baseline and at 12, 24, and 48 hours post-intervention. Sleep quality was assessed at baseline and again at 48 hours, whereas functional mobility (Timed Up and Go test) was evaluated only at 48 hours. Anxiety and fatigue were assessed only at baseline. The intervention was administered by one physiotherapist who was not involved in outcome assessment. All outcome assessments were performed by a second physiotherapist throughout the study. Because all measurements were obtained by the same assessor, inter-rater reliability was not applicable. Only the outcome measures and assessment time points relevant to the predefined objectives of the present report are presented in this manuscript.

Primary outcome

Pain intensity.

Pain intensity was assessed using a 100-mm Visual Analog Scale (VAS), a valid and reliable instrument for measuring acute postoperative pain [10,11]. Scores were recorded at rest and during coughing at each time point. The sensitivity of this scale for dynamically monitoring postoperative pain has been highlighted in recent studies [4].

Secondary outcomes

Oxygen saturation (SpO2).

Peripheral SpO2 was measured at each time point using a portable pulse oximeter (H100B, Edan Instruments, Shenzhen, China), with values averaged from three consecutive readings [12]. Pulse oximetry is a valid and reliable method for non-invasive assessment of peripheral oxygen saturation [13]

Sleep quality, fatigue, and anxiety.

VAS-based assessments have demonstrated acceptable validity and reliability for evaluating acute postoperative symptoms, including anxiety and fatigue, and have been used to monitor changes in perceived sleep quality [14–16].

Functional mobility.

Functional mobility was assessed using standardized single-task Timed Up and Go (TUG) test [17]. Participants stood up from a chair, walked 3 meters, turned around, and returned to a seated position, with completion time recorded in seconds. A research assistant accompanied participants throughout the test to ensure safety. TUG test is a valid and reliable measure of functional mobility in cardiovascular populations [17].

Analgesic use and length of hospital stay (LOS): Analgesic use during the first 48 postoperative hours was categorized as intravenous paracetamol, non-steroidal anti-inflammatory drugs (NSAIDs), and weak opioids (tramadol). Intravenous paracetamol (1000 mg) was administered as part of the standard postoperative analgesic protocol; however, total paracetamol consumption could vary according to individual pain levels and clinical requirements. Rescue tramadol (50 mg) was administered when VAS ≥ 40 mm and repeated as needed. Total paracetamol and tramadol doses were calculated cumulatively (mg), and NSAID use was recorded as yes/no. NSAID administration was not protocolized and was left to the discretion of the treating physician according to routine clinical practice. Analgesic data were verified using nursing records and the hospital information system. LOS was defined as the number of days from surgery to hospital discharge, including both ICU and ward stays. Hospital discharge was determined by the cardiovascular surgery team according to routine institutional clinical criteria and was independent of the study investigators.

Safety monitoring.

Skin reactions (redness, irritation, itching) and other adverse events were monitored and documented. No serious adverse events occurred during the study. Two participants in the ETT group experienced mild skin redness, and one participant in the placebo group reported mild itching. No adverse events were observed in the sham group. None of these events required medical treatment, resulted in premature tape removal, or led to study withdrawal. No patients required ICU readmission or reoperation during the study period, and no major postoperative complications were observed.

Sample size calculation

A priori sample size calculation was performed using G*Power software (v3.1.9.7). Based on the pooled standardized mean difference for postoperative pain after median sternotomy reported by King et al., an effect size of 0.49 was selected as a conservative estimate of the expected between-group difference in the primary outcome for the a priori sample size calculation [18]. With a two-sided α = 0.05 and 80% power (1 − β = 0.80), the required sample size was calculated as 65 participants per group (195 in total). Recruitment continued until the target number of 195 evaluable participants was achieved. Consequently, 203 participants were randomized, and 195 completed the study and were included in the final analysis.

Statistics

Statistical analyses were performed using SPSS (v20.0) and R Studio (v4.5.2). Normality and variance homogeneity were assessed with the Shapiro–Wilk and Levene’s tests. Continuous data are presented as mean ± standard deviation (SD) or median (interquartile range-IQR), and categorical data as frequencies and percentages.

Baseline characteristics were compared using one-way ANOVA, Kruskal–Wallis, χ², or Fisher’s exact tests as appropriate. The primary outcome (VAS) was analyzed using a two-way mixed ANOVA (group × time), which was selected a priori to evaluate between-group, within-group, and group-by-time interaction effects across repeated measurements. Given the balanced study design and equal group sizes, mixed ANOVA was considered appropriate because of its robustness to moderate departures from normality. Bonferroni-adjusted post-hoc comparisons were performed when appropriate. Effect sizes were reported as partial η² and Cohen’s d. SpO2, was analyzed using Friedman test. Because sleep quality, fatigue, TUG, and length of hospital stay data did not satisfy the assumption of normality according to the Shapiro-Wilk test, these variables were summarized as median (interquartile range) and analyzed using non-parametric methods. Sleep quality, fatigue, and TUG were compared using Kruskal–Wallis tests. All analyses were two-tailed (α = 0.05). Analyses were conducted using a modified intention-to-treat (mITT) approach, including all randomized participants who received the allocated intervention and had at least one evaluable post-intervention outcome assessment. Participants with no post-intervention outcome data were excluded because no post-intervention data were available for analysis. No imputation of missing outcome data was performed because only seven participants (3.4%) were lost to follow-up. Therefore, the primary analysis represents a complete-case mITT approach. The final sample (n = 195) met the a priori power requirement.

Results and discussion

A total of 238 patients were assessed for eligibility. Thirty-five patients were excluded (20 did not meet the inclusion criteria, 10 declined to participate, and 5 were excluded for other reasons). Consequently, 203 participants were randomized to the ETT group (n = 67), placebo group (n = 68), or sham group (n = 68).

All randomized participants received their allocated intervention. During follow-up, 2 participants in the ETT group (withdrawal at own request), 3 in the placebo group (2 early discharge, 1 missing data), and 2 in the sham group (1 withdrawal at own request, 1 clinical deterioration) were lost to follow-up. A total of 195 participants (65 per group) were included in the final analysis.

Demographic and clinical characteristics

Baseline demographic and clinical characteristics of the 195 participants are shown in Table 1. Groups were similar in baseline demographics and clinical characteristics. Likewise, baseline resting and coughing VAS scores were comparable.

thumbnail
Table 1. Baseline demographic, surgical, and clinical characteristics of the participants.

https://doi.org/10.1371/journal.pone.0359282.t001

Comparison of pain scores (primary outcome)

At 12, 24, and 48 hours, the ETT group showed lower pain scores at rest and during coughing than the placebo and sham groups (Fig 3).

thumbnail
Fig 3. Changes in postoperative pain scores over time.

Panel A shows VAS pain scores at rest, and Panel B shows VAS pain scores during coughing at baseline and at 12, 24, and 48 hours after surgery.

https://doi.org/10.1371/journal.pone.0359282.g003

Post-hoc analyses showed that pain reduction was driven by the ETT group, with no significant differences between the placebo and sham groups. For pain during coughing, a marked improvement from baseline was observed in the ETT group at 48 hours (Table 2). A significant group × time interaction was found (F(6,384) = 4.12, p = 0.001, partial η² = 0.089).

thumbnail
Table 2. Comparison of post-intervention clinical outcomes between the groups.

https://doi.org/10.1371/journal.pone.0359282.t002

Between-group comparisons demonstrated clinically meaningful reductions in resting pain in the ETT group compared with both control groups at all postoperative time points. At 12 h, the mean difference was −17.8 mm (95% CI: −22.6 to −12.9) versus placebo and −22.6 mm (95% CI: −27.5 to −17.7) versus sham. At 24 h, the corresponding differences were −17.5 mm (95% CI: −21.9 to −13.0) and −22.1 mm (95% CI: −27.1 to −17.2), respectively. At 48 h, the mean differences were −18.5 mm (95% CI: −22.7 to −14.3) versus placebo and −22.2 mm (95% CI: −26.9 to −17.5) versus sham. All observed between-group differences exceeded the reported minimal clinically important difference for acute postoperative pain.

Mobility, sleep, and other clinical outcomes

Functional mobility, psychometric scores, and recovery-related outcomes are summarized in Table 2. The ETT group demonstrated the fastest performance on the TUG test at 48 hours (11.2 s), which was significantly better than that of the other two groups (p = 0.002). Compared with the PT group, the median TUG time was 2.2 seconds shorter (95% CI: −2.8 to −0.7), and compared with the ST group, it was 2.6 seconds shorter (95% CI: −3.1 to −1.2). Sleep quality scores were also higher in the ETT group (65/100) compared with the control groups (p = 0.001).

As shown in Table 3, total paracetamol (p = 0.004) and tramadol (p = 0.038) consumption during the first 48 postoperative hours were significantly lower in the ETT group than in the placebo and sham groups. Compared with both control groups, the median difference in tramadol consumption was −50 mg (95% CI: −50 to −50). NSAID use did not differ between groups (p = 0.112).

thumbnail
Table 3. Total analgesic consumption during the first 48 postoperative hours.

https://doi.org/10.1371/journal.pone.0359282.t003

Total analgesic consumption was lowest in the ETT group (Fig 4). This was also reflected in a shorter median length of hospital stay in the ETT group (median, 4 days; p = 0.042).

thumbnail
Fig 4. Cumulative analgesic consumption during the first 48 postoperative hours.

Panel A shows cumulative paracetamol consumption, and Panel B shows cumulative tramadol consumption. Boxplots represent the median, interquartile range, and whiskers. ETT: Elastic Therapeutic Taping; PT: Placebo Taping; ST: Sham Taping.

https://doi.org/10.1371/journal.pone.0359282.g004

Correlation analysis results

Exploratory correlation analyses were conducted to examine associations between clinical outcomes. Spearman correlation analysis (Table 4) showed a strong positive association between 48-hour VAS pain scores and TUG times (rs = 0.684, p = 0.001), and a strong negative association between pain and sleep quality (rs=−0.712, p = 0.001). LOS was positively correlated with both pain intensity (rs = 0.545, p = 0.003) and mobilization speed (rs = 0.612, p < 0.001).

thumbnail
Table 4. Correlation between Pain, Mobility, and Clinical Recovery (n = 195).

https://doi.org/10.1371/journal.pone.0359282.t004

Overall findings

This 3-arm randomized controlled study demonstrates that ETT significantly reduces post-sternotomy pain at rest and during coughing. The magnitude of pain reduction exceeded the minimal clinically important difference, indicating a clinically meaningful effect. Moreover, reduced opioid requirements in the ETT group support its role as an opioid-sparing adjuvant in the early postoperative period.

Pain control and underlying mechanisms.

The analgesic effect of ETT may be explained by both neurophysiological and biomechanical mechanisms [19]. Continuous cutaneous stimulation may enhance mechanoreceptor activation and inhibit nociceptive input [20]. In the present study, the approximately 20–22 mm reduction in VAS scores observed in the ETT group exceeded the reported minimal clinically important difference of 9.9 mm for acute postoperative pain measured on a 100-mm visual analog scale, indicating a clinically meaningful effect [21].

The significant reduction in movement-evoked pain during coughing suggests that ETT may exert effects beyond sensory modulation. After median sternotomy, the soft tissue undergoes micro-movements continuously stimulating nociceptors [1,6]. ETT uses gentle elevation of the skin and low level of tension applied to alter the mechanical properties of the underlying tissue, thus enhancing proprioception and musculofascial stability [22]. It has been proposed that ETT limits micro-movements and reduces mechanically induced nociceptor activation [23]. ETT enhances proprioceptive input, improving neuromuscular control and suppressing functional pain [24]. Although these neurophysiological and biomechanical mechanisms are biologically plausible and supported by previous studies, they were not directly evaluated in the present study. Therefore, they should be considered as potential explanations for the observed clinical outcomes rather than confirmed mechanisms of action.

The lack of significant differences between the placebo and sham groups suggests that the analgesic effects of ETT were not attributable to expectancy alone [25]. This is consistent with previous studies of patients who have undergone sternotomy [4,6]. In contrast, the inconsistent results of other trials may have been attributable to inadequate taping techniques or suboptimal tape placement that limited tape recoil in the surgical setting [26]. Our findings suggest that biomechanical support provided under appropriate tension may contribute to the observed analgesic effect.

Due to the numerous factors contributing to anxiety post-CABG surgery, it is not surprising that only doing a local intervention is not enough to change this systemic stress response. Even if expectations and psychological coping may alter how someone perceives pain (for example, that idea that someone expects to be able to identify a trigger), the fact that there is no difference in anxiety among the groups indicates that the analgesic effect of ETT is more due to neurophysiological and biomechanical mechanisms [6,27]. However, previous work has shown that, despite reductions in physical pain, improvements in quality of life and psychological outcomes after sternotomy may be slower or more limited, indicating that psychological and trust-related processes should still be considered alongside pain recovery [28]. Pain reduction became evident at 12 hours and progressed up to 48 hours, suggesting a cumulative time-dependent effect. This finding is consistent with biomechanical models proposing that ETT redistributes mechanical stress around the surgical site [1,22,23].

Effective early pain control may limit central sensitization and reduce the risk of chronic postoperative pain, although the transition from acute to chronic pain is multifactorial and influenced by several patient- and surgery-related factors [29,30]. While Parreira et al. argued that ETT is not more effective than placebo, the absence of analgesic effects in the sham and tension-free placebo groups in our study contradicts this view and supports a role for mechanoreceptive stimulation and biomechanical support [25]. ETT after sternotomy has also been associated with improved respiratory comfort [6]. Our findings suggest that ETT may preferentially reduce functional pain components triggered by movement rather than pain at rest.

The marked reduction in total analgesic and tramadol consumption in the ETT group suggests that the intervention may not only improve subjective pain perception but also reduce postoperative analgesic requirements [6]. However, in that study, analgesic consumption reached a plateau in the early postoperative period, whereas our findings demonstrate a continued reduction in analgesic requirements up to 48 hours. This progressive effect more strongly supports the role of ETT as an opioid-sparing adjuvant during early recovery.

In clinical conditions with lower mechanical stress, such as musculoskeletal pain, the analgesic effects of taping are often limited or inconsistent. In contrast, the marked mechanical instability and inflammatory load of the chest wall after sternotomy increase the need for external support, which may explain the more pronounced clinical benefit observed in this population [25]. Especially in older individuals undergoing CABG with multiple comorbidities, reduced tramadol requirements represent a clinically meaningful benefit by lowering the risk of opioid-related complications, including delirium, respiratory depression, and gastrointestinal side effects.

Similar NSAID use across groups suggests that ETT preferentially reduces severe, movement-evoked pain requiring opioids rather than baseline inflammatory pain. Although benefits have been reported in musculoskeletal conditions, our findings indicate that this effect is most evident in reduced rescue opioid use [31,32]. Comparable reductions in postoperative pain have also been observed after abdominal surgery [33].

In contrast, in surgical populations with different biomechanical demands, such as total knee arthroplasty, ETT has not shown a clear advantage in reducing analgesic use [34]. This may reflect the mechanically sensitive nature of post-sternotomy pain, which is continuously stressed by breathing and thoracic expansion. These findings align with previous sternotomy studies, while inconsistencies reported in other surgical populations and meta-analyses likely reflect differences in biomechanical demands and taping techniques [6,25,35]. Thus, the observed effect cannot be explained by expectancy alone.

Functional improvements and proprioceptive input.

The rapid mobilization and improved TUG performance after ETT suggest that its effects extend beyond nociceptive modulation. This is consistent with evidence showing strong associations between kinesiophobia, pain, disability, and reduced quality of life [36].

Our findings align with this perspective; although kinesiophobia was not directly measured. Objective functional measures such as the TUG capture not only muscular performance but also movement-related fear and self-confidence and are therefore key indicators in postoperative rehabilitation [37]. This is consistent with rehabilitation models showing that physical support enhancing postoperative trunk stability can facilitate mobility [38]. However, subjective confidence does not always correlate with objective walking speed, suggesting that functional improvements may reflect not only perceptual factors but also mechanical and proprioceptive inputs [39]. These correlations should be considered exploratory and hypothesis-generating and require confirmation in future studies.

Respiratory patterns and sleep quality: Secondary effect.

Reduced pain with ETT may lessen guarded breathing and promote more effective ventilation, providing a physiological basis for the observed changes in oxygen saturation. After abdominal surgery, Manzano et al. reported only transient SpO2 improvements without sustained between-group differences, whereas structural and ventilatory differences after sternotomy may explain the relatively greater changes observed in our study [40]. In addition, routine postoperative oxygen therapy may create a ceiling effect, limiting the detection of true between-group differences in SpO2 [41].

Postoperative pain is negatively associated with sleep quality, with higher pain strongly disrupting sleep [42]. Consistent with this relationship, reduced pain and improved sleep quality were observed in our study. ETT may indirectly improve sleep by reducing postoperative pain, which is closely associated with postoperative sleep quality [43,44]. Further studies are needed to determine whether this effect is direct or secondary to pain reduction.

Implications for practice

Clinical implications and safety.

The approximately 1-day reduction in LOS observed in the ETT group suggests potential benefits for clinical recovery and healthcare resource utilization. Because LOS is influenced by multiple factors, including postoperative complications, hemodynamic stability, discharge practices, and functional recovery, this finding should be interpreted with caution. Similar LOS reductions have been demonstrated with early mobilization protocols across surgical populations [45]. Although patients in the ETT group experienced shorter hospital stays, the present study was not designed to determine the independent contribution of ETT to discharge timing. Larger studies with adjustment for relevant clinical covariates are needed to confirm this association.

ETT is a noninvasive intervention with no serious adverse events, supporting its safety as part of multimodal analgesia and rehabilitation [46]. Together, these findings suggest that ETT may provide symptomatic and operational benefits during early postoperative recovery after sternotomy. Larger multicenter studies are needed to confirm these effects.

Strengths and limitations

Major strengths of this study include its three-arm randomized design with both placebo and sham control groups, a sample size determined by an a priori power analysis, and the comprehensive assessment of pain, mobility, analgesic consumption, and recovery-related outcomes. Nevertheless, several limitations should be acknowledged. The single-center design and short follow-up limit generalizability and long-term inference. In addition, the trial was registered retrospectively, although no changes were made to the study design, outcomes, or analysis plan after participant enrollment began. Functional mobility was measured with the TUG, whereas kinesiophobia and pain-related avoidance were not evaluated with validated scales; thus, inferences regarding fear of movement remain indirect and hypothesis-generating. All taping was performed by a single physiotherapist aware of group allocation, which may introduce provider bias. In addition, use of a single taping material and tension protocol may limit generalizability to other techniques. Despite these limitations, randomization and the use of placebo and sham control groups were implemented to minimize potential bias. The outcome assessments were performed by a physiotherapist who did not administer the intervention. However, the success of participant and assessor blinding was not formally evaluated. In addition, because ETT and sham taping were applied to different anatomical regions, some participants may have inferred their group allocation. Therefore, the possibility of partial unblinding, particularly for subjective outcome measures, cannot be excluded.

Conclusions

In conclusion, ETT provides clinically meaningful pain reduction after CABG via median sternotomy. The intervention was particularly effective for movement-evoked pain and was associated with reduced analgesic use, improved early mobilization, and a shorter length of hospital stay. Given its noninvasive, low-cost, and safe profile, ETT represents practical adjunct to multimodal postoperative pain management after cardiac surgery. Further multicenter studies with longer follow-up are warranted to confirm long-term clinical and economic benefits.

Supporting information

S2 Checklist. PLOS human participants research checklist.

https://doi.org/10.1371/journal.pone.0359282.s002

(PDF)

S2 Protocol. Original study protocol (Turkish version).

https://doi.org/10.1371/journal.pone.0359282.s004

(PDF)

Acknowledgments

The authors would like to thank the participants and the medical staff at the Department of Cardiovascular Surgery, Bolu Abant Izzet Baysal University, for their cooperation during the study.

Consent for publication: Written informed consent for publication of the clinical photographs was obtained from all participants whose photographs are presented in Fig 2.

References

  1. 1. Zubrzycki M, Liebold A, Skrabal C, Reinelt H, Ziegler M, Perdas E, et al. Assessment and pathophysiology of pain in cardiac surgery. J Pain Res. 2018;11:1599–611. pmid:30197534
  2. 2. Gissing CA, Roos R. Respiratory muscle strength, pain and pulmonary complications in adult patients following median sternotomy during hospital stay: A longitudinal observational study. Bull Fac Phys Ther. 2024;29(1):65.
  3. 3. Othenin-Girard A, Ltaief Z, Verdugo-Marchese M, Lavanchy L, Vuadens P, Nowacka A, et al. Enhanced recovery after surgery (ERAS) protocols in cardiac surgery: Impact on opioid consumption. J Clin Med. 2025;14(5):1768. pmid:40095860
  4. 4. Temel Aksu N, Erdoğan M, Erdoğan A. The effect of kinesio taping on pain, respiratory function, and muscle strength after thoracotomy. Turk Gogus Kalp Damar Cerrahisi Derg. 2023;31(4):507–16. pmid:38075992
  5. 5. Skwiot M. Effectiveness of Kinesio taping for lymphedema in the post-mastectomy patient: A systematic review of randomized controlled trials. J Clin Med. 2025;14(5):1700. pmid:40095723
  6. 6. Brockmann R, Klein H-M. Pain-diminishing effects of Kinesio® taping after median sternotomy. Physiother Theory Pract. 2018;34(6):433–41. pmid:29308962
  7. 7. Hohenschurz-Schmidt D, Draper-Rodi J, Vase L, Scott W, McGregor A, Soliman N, et al. Blinding and sham control methods in trials of physical, psychological, and self-management interventions for pain (article II): A meta-analysis relating methods to trial results. Pain. 2023;164(3):509–33. pmid:36271798
  8. 8. Boutron I, Altman DG, Moher D, Schulz KF, Ravaud P, CONSORT NPT Group. CONSORT statement for randomized trials of nonpharmacologic treatments: A 2017 update and a CONSORT extension for nonpharmacologic trial abstracts. Ann Intern Med. 2017;167(1):40–7. pmid:28630973
  9. 9. Hohenschurz-Schmidt D, Vase L, Scott W, Annoni M, Ajayi OK, Barth J, et al. Recommendations for the development, implementation, and reporting of control interventions in efficacy and mechanistic trials of physical, psychological, and self-management therapies: The CoPPS Statement. BMJ. 2023;381:e072108. pmid:37230508
  10. 10. Kahl C, Cleland JA. Visual analogue scale, numeric pain rating scale and the McGill pain questionnaire: An overview of psychometric properties. Phys Ther Rev. 2005;10(2):123–8.
  11. 11. Chou R, Gordon DB, de Leon-Casasola OA, Rosenberg JM, Bickler S, Brennan T, et al. Management of Postoperative Pain: A clinical practice guideline from the American Pain Society, the American Society of Regional Anesthesia and Pain Medicine, and the American Society of Anesthesiologists’ committee on regional anesthesia, executive committee, and administrative council. J Pain. 2016;17(2):131–57. pmid:26827847
  12. 12. Jubran A. Pulse oximetry. Crit Care. 2015;19(1):272. pmid:26179876
  13. 13. Hess DR. Pulse oximetry: 2023 Year in review. Respir Care. 2024;69(8):1033–41. pmid:38806220
  14. 14. Labaste F, Ferré F, Combelles H, Rey V, Foissac J-C, Senechal A, et al. Validation of a visual analogue scale for the evaluation of the postoperative anxiety: A prospective observational study. Nurs Open. 2019;6(4):1323–30. pmid:31660159
  15. 15. Koo M, Yang S-W. Visual analogue scale. Encyclopedia. 2025;5(4):190.
  16. 16. Alqurashi YD, Dawidziuk A, Alqarni A, Kelly J, Moss J, Polkey MI, et al. A visual analog scale for the assessment of mild sleepiness in patients with obstructive sleep apnea and healthy participants. Ann Thorac Med. 2021;16(2):141–7. pmid:34012480
  17. 17. Bellet RN, Francis RL, Jacob JS, Healy KM, Bartlett HJ, Adams L, et al. Timed Up and Go Tests in cardiac rehabilitation: Reliability and comparison with the 6-Minute Walk Test. JCRP. 2013;33(2):99–105. pmid:23221811
  18. 18. King M, Stambulic T, Hassan SMA, Norman PA, Derry K, Payne DM, et al. Median sternotomy pain after cardiac surgery: To block, or not? A systematic review and meta-analysis. J Card Surg. 2022;37(11):3729–42. pmid:36098374
  19. 19. Li Y, Yin Y, Jia G, Chen H, Yu L, Wu D. Effects of kinesiotape on pain and disability in individuals with chronic low back pain: A systematic review and meta-analysis of randomized controlled trials. Clin Rehabil. 2019;33(4):596–606. pmid:30526011
  20. 20. Luz Júnior MAD, Almeida MOD, Santos RS, Civile VT, Costa LOP. Effectiveness of kinesio taping in patients with chronic nonspecific low back pain: A systematic review with meta-analysis. Spine (Phila Pa 1976). 2019;44(1):68–78. pmid:29952880
  21. 21. Myles PS, Myles DB, Galagher W, Boyd D, Chew C, MacDonald N, et al. Measuring acute postoperative pain using the visual analog scale: The minimal clinically important difference and patient acceptable symptom state. Br J Anaesth. 2017;118(3):424–9. pmid:28186223
  22. 22. Alqahtani AS, Parveen S. Kinesio taping as a therapeutic tool for masticatory myofascial pain syndrome-An insight view. Int J Environ Res Public Health. 2023;20(5):3872. pmid:36900882
  23. 23. Pogatzki-Zahn EM, Segelcke D, Schug SA. Postoperative pain-from mechanisms to treatment. Pain Rep. 2017;2(2):e588. pmid:29392204
  24. 24. Ghai S, Ghai I, Narciss S. Influence of taping on joint proprioception: A systematic review with between and within group meta-analysis. BMC Musculoskelet Disord. 2024;25(1):480. pmid:38890668
  25. 25. Parreira P do CS, Costa L da CM, Hespanhol LC Jr, Lopes AD, Costa LOP. Current evidence does not support the use of Kinesio Taping in clinical practice: A systematic review. J Physiother. 2014;60(1):31–9. pmid:24856938
  26. 26. Lu Z, Li X, Chen R, Guo C. Kinesio taping improves pain and function in patients with knee osteoarthritis: A meta-analysis of randomized controlled trials. Int J Surg. 2018;59:27–35. pmid:30273684
  27. 27. Sakyi R, Boateng EA, Diji AK-A, Afful KA, Nimoh VA, Ajanaba PA, et al. Pain expectations, experiences and coping strategies used by post-operative patients: A descriptive phenomenological study. PLoS One. 2025;20(6):e0298780. pmid:40493610
  28. 28. Viana LBDR, Oliveira EJSG de, Oliveira CMB de, Moura ECR, Viana LHL, Nina VJ da S, et al. Assessment of pain and quality of life in patients undergoing cardiac surgery: A cohort study. Rev Assoc Med Bras (1992). 2023;69(3):473–8. pmid:36820781
  29. 29. Reddi D. Preventing chronic postoperative pain. Anaesthesia. 2016;71 Suppl 1:64–71. pmid:26620149
  30. 30. Rosenberger DC, Pogatzki-Zahn EM. Chronic post-surgical pain - update on incidence, risk factors and preventive treatment options. BJA Educ. 2022;22(5):190–6. pmid:35496645
  31. 31. Lim ECW, Tay MGX. Kinesio taping in musculoskeletal pain and disability that lasts for more than 4 weeks: Is it time to peel off the tape and throw it out with the sweat? A systematic review with meta-analysis focused on pain and also methods of tape application. Br J Sports Med. 2015;49(24):1558–66. pmid:25595290
  32. 32. Macedo L de B, Richards J, Borges DT, Melo SA, Brasileiro JS. Kinesio Taping reduces pain and improves disability in low back pain patients: A randomised controlled trial. Physiotherapy. 2019;105(1):65–75. pmid:30348455
  33. 33. Yılmaz S, Terzioğlu F. The effects of Kinesio taping and breathing exercises on pain management after gynaecological abdominal surgery: A randomized controlled study. Int J Nurs Pract. 2023;29(2):e13088. pmid:35929048
  34. 34. Cakmak MF, Cigdem-Karacay B. The effect of kinesio taping on edema, pain, and functionality after total knee arthroplasty: A randomised sham-controlled double blinded clinical study. J Orthop Sci. 2024;29(4):983–9.
  35. 35. Kandeel M, Marzok M, Afzal S, Meligy A, Mahmoud M, Albokhadaim I, et al. A systematic review and meta-analysis of the efficacy of Kinesio Taping for pain management and pressure pain threshold in myofascial pain syndrome. Pain Res Manag. 2025;2025:8881632. pmid:40860981
  36. 36. Luque-Suarez A, Martinez-Calderon J, Falla D. Role of kinesiophobia on pain, disability and quality of life in people suffering from chronic musculoskeletal pain: A systematic review. Br J Sports Med. 2019;53(9):554–9. pmid:29666064
  37. 37. Singh A, Xie Y, Mazzola E, Wang S, McAllister M, Pezeshkian F, et al. Gait speed as a measure of frailty and outcomes after lung resection. Ann Surg Oncol. 2025;32(6):4181–8. pmid:40016615
  38. 38. Park S-J, Kim E-K, Kim Y-M, Kang D-Y. Effects of trunk stability exercises and thoracic manipulation on spine flexibility in chronic low back pain patients. KSPM. 2021;16(2):115–23.
  39. 39. Finet M, Bellicha A, Sage E, Glorion M, Kennel T, Labro M, et al. Comprehensive assessment of postoperative mobility during the first days after mini-invasive lung surgery: A prospective observational study. J Clin Anesth. 2023;86:111048. pmid:36716650
  40. 40. Manzano RM, Carvalho CRF de, Saraiva-Romanholo BM, Vieira JE. Chest physiotherapy during immediate postoperative period among patients undergoing upper abdominal surgery: Randomized clinical trial. Sao Paulo Med J. 2008;126(5):269–73. pmid:19099160
  41. 41. Ahmad AM. Essentials of physiotherapy after thoracic surgery: What physiotherapists need to know. A narrative review. Korean J Thorac Cardiovasc Surg. 2018;51(5):293–307. pmid:30402388
  42. 42. Pan Z, Liu Q, Chen Y, He H, Yin J, Li Y. Correlation between pain sensitivity and postoperative sleep disturbance in adult patients undergoing intestinal polypectomy under general anaesthesia: A prospective cohort study. BMJ Open. 2025;15(7):e100753. pmid:40617606
  43. 43. Soh PQP, Wong WHT, Roy T, Tam WWS. Effectiveness of non-pharmacological interventions in improving sleep quality after cardiac surgery: A systematic review and meta-analysis. J Clin Nurs. 2024;33(6):2084–98. pmid:38477050
  44. 44. Bjurström MF, Irwin MR. Perioperative pharmacological sleep-promotion and pain control: A systematic review. Pain Pract. 2019;19(5):552–69. pmid:30762974
  45. 45. Schweickert WD, Pohlman MC, Pohlman AS, Nigos C, Pawlik AJ, Esbrook CL, et al. Early physical and occupational therapy in mechanically ventilated, critically ill patients: A randomised controlled trial. Lancet. 2009;373(9678):1874–82. pmid:19446324
  46. 46. Eden A. ACPRC scoping review of post-operative physiotherapy in people undergoing cardiac surgery. ACPRC J. 2023;55(1):114–50.