Correction
20 Aug 2020: Park KA, Eum SY, Oh H, Cho MH, Chang HS, et al. (2020) Correction: Factors affecting online health community participation behavior in patients with thyroid cancer. PLOS ONE 15(8): e0238273. https://doi.org/10.1371/journal.pone.0238273 View correction
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Abstract
Globally, cancer patients obtain much of their disease information online. Online health communities allow patients to share questions and information about diseases. However, there have been few studies on the factors affecting online health community participation behavior in cancer patients. Online social networking is associated with mental health problems, and patients with thyroid cancer experience high levels of distress, anxiety and depression. The purpose of this study was to investigate factors associated with use of online health communities by patients with thyroid cancer to understand the characteristics of patients participating in such online communities. A questionnaire survey was completed by 114 thyroid cancer patients admitted for surgery at a general hospital in Seoul, Korea. General characteristics, clinical characteristics, attitude toward cancer, distress, and anxiety and depression scores of patients who joined an online health community (user group) and patients who did not (non-user group) were compared. The factors affecting online health community participation were education (p = 0.049), tumor size (p = 0.010), attitude toward cancer (p = 0.022), and anxiety and depression (p = 0.021). The average score of satisfaction with the online health community was 4.25 of 5. The user group had larger tumors, a high awareness of the risk of thyroid cancer, and high levels of anxiety and depression. Patients who actively used the online health community have relatively larger cancer size and had higher levels of mental stress. As such patients are often very anxious and depend heavily on the gathered information, the quality of this information is important. Healthcare professionals need to develop appropriate interventions for patients participating in the online health community.
Citation: Park KA, Eum SY, Oh H, Cho MH, Chang H-S, Lee YS, et al. (2020) Factors affecting online health community participation behavior in patients with thyroid cancer. PLoS ONE 15(6): e0235056. https://doi.org/10.1371/journal.pone.0235056
Editor: Michio Murakami, Fukushima Medical University School of Medicine, JAPAN
Received: October 16, 2019; Accepted: June 8, 2020; Published: June 24, 2020
Copyright: © 2020 Park et al. This is an open access article distributed under the terms of the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are credited.
Data Availability: The authors confirmed that some access restrictions apply to the data underlying the findings. The data from this research study cannot be shared publicly available due to concerns of participant confidentiality. Data from this research contain potentially identifying and sensitive patient information related to medical records. This study was approved by the Ethics Committee of Gangnam Severance Hospital (email: gsirb@yuhs.ac) on the basis that participants’ data was only accessible by the research team. If there is a researcher who wants to receive the data of this study, contact the corresponding author (MEDILYS@yuhs.ac). Data are available from the Gangnam Severance Hospital Ethics Committee for researchers who meet the criteria for access to confidential data.
Funding: The author(s) received no specific funding for this work.
Competing interests: The authors have declared that no competing interests exist.
Introduction
The population of internet users continues to increase globally, and health care services are also becoming more internet-centric [1]. Patients who want to know about diseases usually obtain information from the internet [2]. The Internet has become an important medium for sharing health information and has also affected patients’ treatment decisions [3]. As more people connect through internet networks, hospitals are offering websites to provide medical information. However, as most of the hospital sites provide limited information, it is difficult for patients to find details such as costs and waiting times [4,5].
Online health communities offer a virtual environment in which patients with common interests freely communicate and share information and knowledge [6]. Patients can easily get support from peers through online health community [6,7]. Therefore, many patients participate in an online health community of others with shared experiences, and healthcare professionals want to provide services using an online health community. However, to provide online services for patients, it is necessary to know what kind of people are using online health communities. People have different interests and preferences, and internet use differs according to sex, age, and region [8]. Internet service providers are building big data based on user behavior in various areas and are using big data to make various customized advertisements [9]. Healthcare professionals will also be able to plan appropriate interventions for online users if they are aware of the characteristics of patients who are joining and using online communities.
In previous studies, online social networking has been associated with several mental illnesses such as depression and anxiety, as well as with low self-esteem [10,11]. Whether mental illness is causing online social networking or whether social online networking is causing mental illness is unclear. However, people using online social networking are emotionally vulnerable, and patients who join an online health community can be predicted to be emotionally vulnerable. Research on online health communities shows that the internet is an important tool for emotional intervention, and internet-mediated interventions have a positive effect on depression and anxiety [12–15]. However, few studies have focused on the characteristics of online health community users.
With the development of diagnostic technology worldwide, the incidence of thyroid cancer has been steadily increasing due to increased detection [16,17]. In Korea, thyroid cancer detection has increased rapidly and has shown the highest cancer incidence since 2009 [18]. Thyroid cancer is often described as a good cancer because it has a good prognosis and a good survival rate [19]. However, patients with thyroid cancer felt negative feelings and isolation about the fact that thyroid cancer represented as good cancer [19]. Patients with thyroid cancer experience high levels of distress and worry, despite having a good prognosis, and have more prevalent anxiety and depression than other cancers [20–22]. Cancer patients feel psychological pain such as anxiety and depression and seek social support [23]. Analyzing the characteristics of subscribers of a thyroid cancer community will help identify the mental health and needs of thyroid cancer patients.
The purpose of this study was to investigate factors associated with use of online health communities by patients with thyroid cancer to understand the characteristics of such patients participating in an online health community. In this study, we compared the characteristics, attitude toward cancer, distress, depression, and anxiety of online-community user and non-user groups. We also described the degree of online-community activity of the online-community user group and their satisfaction with the online community.
Materials and methods
Setting and participants
This study compares the characteristics of online health community user and non-user groups. The online health community in this study refers to the ‘Thyroid Family,’ established in April 2012 at the internet portal site NAVER [24]. The ‘Thyroid family’ was established in Naver, Korea’s largest portal site. The number of members was about 15,000, and the highest online community activity score among thyroid cancer-related online communities in Naver was selected for this study. The ‘Thyroid Family’ is operated by Gangnam Severance Medical Team for patients with thyroid cancer. The online health community consists of professional opinion columns, online booklets, patient experiences, and a Q&A board. Patients were divided according to subscription to the online health community. Those who joined the online health community were classified in the user group, and those who did not join the online health community were classified in the non-user group.
A questionnaire survey was conducted with 114 thyroid cancer patients aged 18 years or older, admitted for surgery from September 18 to November 13, 2017 at Gangnam Severance Hospital, Yonsei University Health System, Korea. To be eligible to participate, respondents required the ability to read and respond to questionnaires. A questionnaire was given to 120 patients admitted to surgery for thyroid cancer. Six patients who refused to participate in the study were excluded. All patients were informed of the guidelines for online communities, and exposure times may vary depending on the individual’s internet search and online use. A survey was conducted researcher knowledge of patient enrollment in an online community. There was no compensation for patient participation in the study. The questionnaire was completed before surgery for thyroid cancer.
This study was approved by the Institutional Review Board of Yonsei University Gangnam Severance Hospital (IRB No. 2017-0368-002). Participants were informed that participation was voluntary and were asked to complete the questionnaire in private. Participants provided written informed consent and contact details (email address and telephone number). Data were coded, and safety monitoring was performed every six months.
Survey instrument
The questionnaire consisted of 33 items, including general characteristics, clinical characteristics, characteristics of the online health community, satisfaction with the online health community, attitude toward cancer, distress, and anxiety and depression. Standardized questionnaire tools were used to measure attitude toward cancer, distress, and the HADS (Hospital Anxiety and Depression Scale) score.
Characteristics of the online health community consisted of the reason for joining the community, the time of joining the community, the degree of community activity, and the level of satisfaction with the community. The measurement tool for assessing quality characteristics that affect satisfaction consisted of nine items and was designed by An et al. (2007) for use in a company internet community site survey [25]. The items addressed by the tool were convenience, reliability of information, usefulness, service playability, site type property, brand reputation, interactivity, satisfaction, and willingness to use in the future. Scores were evaluated using a five-point Likert scale where a higher score indicated greater satisfaction. Cronbach’s α = 0.927 indicated the reliability of the satisfaction evaluation tool.
The measurement tool used to measure attitude toward thyroid cancer was based on a survey tool developed by Suh et al. (1998) and modified by specialists, including one medical specialist and four nurses [26]. The tool consisted of four items related to general attitude toward cancer and six items related to attitude toward early detection and prevention of cancer. Scores were evaluated using a five-point Likert scale where a higher score indicated that the responder was more aware of the risk of thyroid cancer and was positive toward early detection and prevention of thyroid cancer. Cronbach’s α = 0.809 indicated the reliability of the tool to measure attitude toward thyroid cancer.
Distress Thermometer were developed to efficiently measure psychosocial distress and have proven to be an effective tool for screening for cancer-related distress [27, 28]. The Korean version of the Distress Thermometer was used in this study. The degree of psychological distress experienced by patients during the previous week was reported on a visual analogue scale from 0–10, with 0 being "no distress" and 10 being "extreme distress" [29]. Distress scores ≥4 means severe stress, so all patients with distress scores ≥4 were recommended psychological counseling after discharge.
The Hospital Anxiety and Depression Scale (HADS) is a tool for assessing the severity and symptoms of anxiety and depression and offers high sensitivity and specificity [30]. The Hospital Anxiety and Depression Scale (HADS) consists of 14 items, with one subscale of seven items measuring depression (HAD-D) and one subscale of seven items measuring anxiety (HAD-A). Each question consists of four points from 0–3 depending on the severity of the symptoms. The higher the score, the more severe the symptoms [31]. Cronbach’s α = 0.906 indicated the reliability of the tool to measure The Hospital Anxiety and Depression Scale. All patients with HADS scores ≥11 received recommended psychological counseling after discharge.
Data analysis
The analysis was done using the IBM Statistical Package for Social Sciences (SPSS) Statistics version 25.0. Differences according to general characteristics and disease-related characteristics of the experimental and control groups were analyzed using the χ2 test, Fisher’s exact test, and linear by linear association test. Independent t-tests were used to investigate differences in attitude toward thyroid cancer, distress, and anxiety and depression scores. Logistic regression analysis was used to determine the actual factors affecting online health community usage.
Results
Patient characteristics
General characteristics of the 114 patients were as follows: 66.7% were female, age ranged from 18–73 years, the most common age group was 30–39 years (42.1%), the majority were college graduates (78.1%), and the majority had a spouse (82.5%). Most patients had papillary carcinoma (96.5%), 49.1% underwent less than total thyroidectomy, and 56.1% had a tumor size less than 1 cm in diameter. Moreover, 14.0% had direct family members with a history of thyroid cancer. Of the 114 patients, 44 enrolled in an online health community (38.6%), and 93.2% of those enrolled used the online health community as an information source (Table 1).
Characteristics of the online health community-user group
Most subjects in the online health community-user group were registered in only one thyroid cancer online health community (65.9%), and participation time was highest two months before surgery (43.2%). The largest number of respondents found the online health community through an internet search (47.7%), and half (50.0%) of respondents said that they accessed the community more than once a day (Table 2).
Attitude toward thyroid cancer, distress, and HADS
The online health community-user group was more aware of risk of thyroid cancer but also had a positive attitude toward early detection and prevention of the thyroid cancer. The online health community-user group had higher depression and anxiety scores and distress levels (Table 3). The HADS depression mean score of the user group was 8.09 and the HADS depression mean score of non-user group was 5.70 (p = 0.002), and the HADS anxiety mean score of the user group was 8.95 and the HADS anxiety mean score of non-user group was 6.79 (p = 0.004).
Factors affecting online health community subscription
Factors influencing online health community usage were education, tumor size, attitude toward cancer, anxiety, and depression. Online health community subscription was 4.3 times more likely in ≥college graduates than ≤high school graduates (B = 1.464, p = 0.049). Patients with tumors greater than 1 cm in diameter used an online health community 4.1 times more those with tumors less than 1 cm in diameter (B = 1.415, p = 0.010). In addition, those with higher attitude scores for thyroid cancer (B = 0.162, p = 0.022) and higher HADS score were also more likely to use the online health community (B = 0.102, p = 0.021) (Table 4).
Online health community satisfaction
Satisfaction with the online health community among the online health community-user group was generally high, with an average of 4.25 points on a five-point Likert scale. The perceived usefulness of the online health community scored 4.48 points out of a possible five points, and the intention to continue use scored 4.39 out of a possible five points (Table 5).
Discussion
The use of online health communities was affected by education, tumor size, attitude toward thyroid cancer, anxiety, and depression. Most patients in the online health community-user group were college education or higher. In previous surveys, 99% non-internet users had a high school education or less, and college education patients were almost 3 times more likely to use the internet than those with a high school education or less. [8, 32]. College educated people get a lot of information online, and they seem to be more likely to join the online health communities.
Thyroid papillary cancer is the most common of thyroid cancers, and papillary microcarcinoma of less than 1cm are low risk of metastasis and sometimes observation is recommended without immediate surgery [33]. However, if the size of the thyroid papillary cancer is more than 1cm, the possibility of lymph node metastasis increases [34]. Patients with tumor size greater than 1 cm had a higher rate of online health community participation, possibly due to the belief that their disease was more serious and frightening than those with tumor size less than 1 cm.
People with a positive attitude toward early detection and prevention were also more likely to join an online health community in response to a cancer diagnosis. Patients with a strong desire to promote health are more active in searching for disease-related information [35]. The online user group showed the highest levels of anxiety and depression. When diagnosed with cancer, patients are faced with treatment burdens and the possibility of death [36]. Thyroid cancer patients often experience anxiety and depression after diagnosis [37,38]. Newly diagnosed breast cancer patients are also more likely to develop anxiety and depression [39]. The patients in this study consisted of preoperative patients, and the online community-user group consisted of preoperative patients who were diagnosed with thyroid cancer and showed mild anxiety and depressive symptoms. Joining an online health community is one way to reduce anxiety and depression by gathering information and sharing experiences with others. The motivation factor for online health community activity is to gain information and make changes in response to a cancer diagnosis [40]. Previous study has shown that health-related internet use was associated with depression, and those who are more vulnerable to health anxiety can choose online health resources [11]. If medical professionals can select patients who are at high risk for anxiety and depression from an online health community before surgery, timely intervention can be achieved.
Online health communities are easily accessible via the internet, and members can exchange information and emotional support. However, because inaccurate information is also common in online health communities, credibility must be secured for sites providing medical information to be effective [41]. It is sometimes difficult for people to determine what is correct, because information is sometimes provided for commercial purposes. Moreover, emotionally unstable patients are easily tricked and often have difficulty in discerning accurate information. In previous research, the quality of a website for thyroid cancer was found to be very different depending on the provider of website, and most of the websites were of low quality [42]. If patients in critical condition join an online health community that is not properly managed, they may be misled with wrong or incomplete information. Therefore, it is important for medical staff to improve the reliability of online health communities and guide members to share correct information and communication. The online health community accessed by subjects of this study was operated by medical staff, and satisfaction with the site among the online health community-user group was also high. When people experience the benefits of community services, the frequency of use of services increases [43]. In this study, more than half of the online health community-user group visited the site more than once a day, which shows that patients were self-directed in looking for the online health community, and that the online health community had a significant impact on patients.
Participation in online health communities has been shown to have a positive effect on knowledge sharing, and the social support provided by internet communities has been shown to increase self-efficacy and self-care behaviors [44,45]. Peer-support not only helps patients cope effectively with stressful situations, but it can also reduce depression and improves health status [46,47]. Technology is continuously changing, and the methods of implementing interventions are becoming more diverse. The use of the internet has increased, and online communication between patients and healthcare providers has also increased [48]. More research is needed on the characteristics of cancer patients who join an online health community and how the online health community affects cancer patients. Through continuous efforts and research, the online health community should be able to broaden its scope as an appropriate intervention for patients.
Limitation
There are several limitations of the study. First, because the study utilized a pre-established online health community called a ‘Thyroid Family,’ which has been managed by a university affiliated hospital, the community does not represent the online community in general. Second, the results of this study are difficult to be generalized to other online disease-related communities because the characteristics of health communities are widely varied by multiple pathophysiological and societal factors. Third, as a nature of an observational study based on questionnaire, it is hard to claim any causality in our observations. More research is necessary to investigate the characteristics of people who are actively involved in an online health community.
Conclusion
This study compared the characteristics of thyroid cancer patients who joined the online health community and those who did not, and identified factors that influenced the online health community participation behavior. Patients who actively used the online health community have relatively larger cancer size and more severe anxiety and depression. Healthcare professionals need to develop appropriate interventions for patients participating in the online health community.
Acknowledgments
We thank Young Ja Oh, Hanna Kim, and Yoonhee Park, Department of Nursing, Gangnam Severance Hospital, for assistance in the online community management.
References
- 1. Bujnowska-Fedak MM, Trends in the use of the Internet for health purposes in Poland. BMC Public Health. 2015;27(15):194.
- 2. AlGhamdi KM, Moussa NA. Internet use by the public to search for health-related information. Int J Med Inform. 2012;81(6):363–73. pmid:22217800
- 3. Hank S, Almog C, John M, Christina W, Elisa RP. Decision-making in breast cancer surgery: Where do patients go for information? AM surg. 2016;82(5):397–402. pmid:27215718
- 4. Kim JM, Ban CH. Usability Evaluation for Hospital Web sites in Korea. Journal of Korea Institute of Information and Communication Engineering. 2011;15(11):2426–2432.
- 5. Norum J, Evaluation of Norwegian cancer hospitals web sites and explorative survey among cancer patients on their use of the internet. J Med Internet Res. 2001;3(4):E30. pmid:11772545
- 6. Lobchuk M, McClement S, Rigney M, Copeland A, Bayrampour H. A Qualitative Analysis of "Naturalistic" Conversations in a Peer-Led Online Support Community for Lung Cancer. Cancer Nurs. 2015;38(5):E21–31. pmid:25254411
- 7. van Eenbergen MC, van de Poll-Franse LV, Heine P, Mols F. The Impact of Participation in Online Cancer Communities on Patient Reported Outcomes: Systematic Review. JMIR Cancer. 2017;28;3(2):e15. pmid:28958985
- 8.
2017 Survey on the Internet Usage Summary Report. Korea, Ministry of Science and ICT, Korea Internet & Security Agency (KISA). [cited 2018 May 2]. https://www.kisa.or.kr/eng/usefulreport/surveyReport_View.jsp?cPage=1&p_No=262&b_No=262&d_No=81&ST=&SV=.
- 9. Dalessandro B, Hook R, Perlich C, Provost F. Evaluating and Optimizing Online Advertising: Forget the Click, but There Are Good Proxies. Big Data. 2015;3(2):90–102. pmid:27447433
- 10. Pantic I, Online social networking and mental health. Cyberpsychol Behav Soc Netw. 2014;17(10):652–7. pmid:25192305
- 11. Bessière K, Pressman S, Kiesler S, Kraut R. Effects of internet use on health and depression: a longitudinal study. J Med Internet Res. 2010;12(1):e6. pmid:20228047
- 12. See comment in PubMed Commons below Hong Y, Peña-Purcell NC, Ory MG. Outcomes of online support and resources for cancer survivors: a systematic literature review. Patient Educ Couns. 2012;86(3):288–96. pmid:21798685
- 13. van Eenbergen MC, van de Poll-Franse LV, Heine P, Mols F. The impact of participation in online cancer communities on patient reported outcomes: Systematic Review. JMIR Cancer. 2017;28:3(2):e15. pmid:28958985
- 14. Griffiths KM, Calear AL, Banfield M. Systematic review on internet support groups(ISGs) and depression(1): Do ISGs reduce depressive symptoms? J Med Internet Res. 2009;30:11(3):e40. pmid:19793719
- 15. Algtewi E, Owens J, Baker SR. Online support groups for head and neck cancer and health-related quality of life. Qual Life Res. 2018;26(9):2351–2362.
- 16. Chen AY, Jemal A, Ward EM. Increasing incidence of differentiated thyroid cancer in the United States, 1998–2005. Cancer 2009;115(16):3801–7. pmid:19598221
- 17. Leenhardt L, Grosclaude P. Epidemiology of thyroid carcinoma over the world. Ann Endocrinol(Paris) 2011;72:136–48.
- 18. Jung KW, Won YJ, Kong HJ, Oh CM, Seo HG, Lee JS. Cancer statistics in Korea, incidence, mortality, survival and prevalence in 2010. Cancer Res Treat 2013;45(1):1–14. pmid:23613665
- 19. Randle RW, Bushman NM, Orne J, Balentine CJ, Wendt E, Saucke M, et al. Papillary Thyroid Cancer: The Good and Bad of the "Good Cancer".Thyroid. 2017;27(7):902–907. pmid:28510505
- 20. Buchmann L, Ashby S, Cannon RB, Hunt JP. Psychosocial distress in patients with thyroid cancer. Otolaryngol Head Neck Surg. 2015;152(4):644–9. pmid:25573679
- 21. Papaleontiou M, Reyes-Gastelum D, Gay BL, Ward KC, Hamilton AS, Hawley ST, et al. Worry in Thyroid Cancer Survivors with a Favorable Prognosis. Thyroid. 2019;29(8):1080–1088. pmid:31232194
- 22. Ryu M, Hwang JI. Cancer site differences in the health-related quality of life of Korean cancer survivors: Results from a Population-based Survey. Public Health Nurs. 2019;36(2):144–154. pmid:30515874
- 23. Mardani-Hamooleh M, Heidari H. Psychosocial Distress as a Factor in Patients With Cancer Seeking Support: A Hermeneutic Study. J Adv Pract Oncol. 2017;8(7):680–686. pmid:30333931
- 24.
Naver cafe [cited 2019 September 1] http://cafe.naver.com/thyroidfamily.
- 25. An US, Jang HS, Oh JC. A Study on the Relationship between Service Quality Characteristics of Internet Brand Community and Continuance of User. Journal of Commodity Science and Technology. 2007;25(4):99–112.
- 26. Suh SR, Chung BY, So HS, Tae YS. A study to advance the development of educational programs for the early detection and prevention of the five major cancer in Korea. J Korean Acad Adult Nurs. 1998;10:268–80.
- 27. Yu ES, Shim EJ, Kim HK, Hahm BJ, Park JH, Kim JH. Development of guidelines for distress management in Korean cancer patients. Psychooncology 2012;21:541–9. pmid:21351189
- 28. O’Donnell E. The distress thermometer: a rapid and effective tool for the oncology social worker. Int J Health Care Qual Assur. 2013;26(4):353–9. pmid:23795426
- 29.
National Comprehensive Cancer Network (NCCN). Clinical practice Guidelines in oncology. 2013;Distress Management. [cited 2017 September 1] https://www.nccn.org/patients/resources/life_with_cancer/pdf/nccn_distress_thermometer.pdf
- 30. Bjelland I, Dahl AA, Haug TT, Neckelmann D. The validity of the Hospital Anxiety and Depression Scale. An updated literature review. J Psychosom Res. 2002 Feb;52(2):69–77. pmid:11832252
- 31. Zigmond AS, Snaith RP, The hospital anxiety and depression scale. Acta Psychiatr Scand. 1983;67(6):361–370. pmid:6880820
- 32. Fogel J, Albert SM, Schnabel F, Ditkoff BA, Neugut AI. Use of the Internet by women with breast cancer. J Med Internet Res. 2002 Apr-Nov;4(2):E9. pmid:12554556
- 33. Ito Y, Miyauchi A, Oda H, Low-risk papillary microcarcinoma of the thyroid: A review of active surveillance trials. Eur J Surg Oncol. 2018 Mar;44(3):307–315. pmid:28343733
- 34. Feng JW, Yang XH, Wu BQ, Sun DL, Jiang Y, Qu Z. Predictive factors for central lymph node and lateral cervical lymph node metastases in papillary thyroid carcinoma. Clin Transl Oncol. 2019 Nov;21(11):1482–1491. pmid:30879178
- 35. Lee MK, Kim YE. A Study on effects of disease information use on the internet: Based on the protection motivation theory, Journal of Communication Science. 2009;9(4):506–539.
- 36. Shaha M, Cox CL. The omnipresence of cancer. Eur J Oncol Nurs. 2003;7(3):191–6. pmid:12932481
- 37. Drabe N, Steinert H, Moergeli H, Weidt S, Strobel K, Jenewein J. Perception of treatment burden, psychological distress, and fatigue in thyroid cancer patients and their partners–effects of gender, role, and time since diagnosis. Psychooncology. 2016;25(3):203–9.
- 38. Seok JH, Choi WJ, Lee YS, Park CS, Oh YJ, Kim JS, et al. Relationship between negative mental adjustment to cancer and distress in thyroid cancer patients, Yonsei Med J. 2013;54(3):658–664. pmid:23549811
- 39. Jacob L, Kalder M, Kostev K. Incidence of depression and anxiety among women newly diagnosed with breast or genital organ cancer in Germany. See comment in PubMed Commons belowPsychooncology. 2017;26(10):1535–1540.
- 40. Harkin LN, Braver K, Dey P, Choong K. Navigating cancer using online communities: a grounded theory of survivor and family experiences. J Cancer Surviv. 2017;11(6):658–669. pmid:28470506
- 41. Jeong SH, Kim JE, Kim TY, Park SY, Shin YJ, Lee SY. Survey on the consumer preference for the internet health information of the patients’ online community members. Healthc Inform Res. 2007;13(3):207–220.
- 42. Kuenzel U, Monga Sindeu T, Schroth S, Huebner J, Herth N. Evaluation of the Qualtiy of Online Information for Patients with Rare Cancers: Thyroid Cancer. J Cancer Educ. 2018;33(5):960–966. pmid:28120139
- 43. Wu H, Lu N. Service provision, pricing, and patient satisfaction in online health communities. Int J Med Inform. 2018: 110:77–89. pmid:29331257
- 44. Yoo S, Oh J, Hong S. The Effect of Service Characteristics on Knowledge Sharing Activity and Participation Intention in Internet Community, Journal of Korea Service Management Society. 2006;7(4):153–175.
- 45. Yu JO, Cho YB. The effect of an internet community on knowledge, self-efficacy and self care behavior in workers with hypertension. Taehan Kanho Hakhoe Chi. 2005;35(7):1258–67. pmid:16418552
- 46. Hoey LM, Ieropoli SC, White VM, Jefford M. Systematic review of peer-support programs for people with cancer. Patient Educ Couns. 2008;70(3):315–37. pmid:18191527
- 47. Winzelberg AJ, Classen C, Alpers GW, Roberts H, Koopman C, Adams RE, et al. Evaluation of an internet support group for women with primary breast cancer. Cancer. 2003;97(5):1164–73. pmid:12599221
- 48. Beckjord EB, Finney Rutten LJ, Squiers L, Arora NK, Volckmann L, Moser RP, et al. Use of the internet to communicate with health care providers in the United States: Estimates from the 2003 and 2005 health information national trends surveys (HINTS). J Med Internet Res. 2007;9(3):e20. pmid:17627929