| Literature DB >> 35771768 |
Azam Bazrafshani1, Sirous Panahi1, Hamid Sharifi2, Effat Merghati-Khoei3.
Abstract
Online social networks have been used to enhance human immunodeficiency virus (HIV) and acquired immunodeficiency syndrome (AIDS) prevention, diagnosis, and treatment programs worldwide. This study aimed to develop a conceptual model of using online social networks in improving health literacy and medication adherence among people living with HIV/AIDS in Iran. This mixed-method sequential exploratory study was conducted in three phases. Firstly, a series of semi-structured interviews with a purposive sample of 29 HIV-positive patients were conducted to investigate the perceptions and experiences of HIV-positive patients about using online social networks to support health literacy and medication adherence. Thematic analysis was used to analyse qualitative interviews, extract potential components, and design a conceptual model. Then, a Delphi study with 27 HIV-positive patients was subsequently conducted to examine the consensus of patients on the proposed model. Finally, the trustworthiness and credibility of the proposed model were reviewed and evaluated by expert panel members from epidemiology and public health. Seven themes and 24 sub-themes emerged from the qualitative interviews. Five themes encompassed components of online social networks that supported communication and information-seeking behaviour of people living with HIV/AIDS. The two other themes encompassed social support and health-related outcomes including medication adherence. The credibility of the proposed conceptual model was confirmed methodologically using the expert panel and Delphi technique. Our findings highlighted that using online social networks has empowered Iranian people living with HIV/AIDS, making them more connected, safe, and able to access HIV/AIDS-related information and services. The role of online social networks in improving health literacy and medication adherence was also demonstrated in a conceptual model to understand the supportive components of online social networks in the HIV care continuum as well as customized interventions to improve the success of antiretroviral therapies.Entities:
Mesh:
Year: 2022 PMID: 35771768 PMCID: PMC9246123 DOI: 10.1371/journal.pone.0261304
Source DB: PubMed Journal: PLoS One ISSN: 1932-6203 Impact factor: 3.752
Demographic characteristics of a qualitative sample of PLWH in Iran.
| Demographic and behavioural characteristics | Frequency (%) |
|---|---|
| Recruitment site | |
| Imam Khomeini Hospital | 21 (72.4) |
| Zam Zam Clinic | 8 (27.6) |
| Residence at the time of interviews | |
| Tehran | 20 (69.0) |
| Ahwaz | 4 (14.0) |
| Karaj | 1 (3.4) |
| Bushehr | 1 (3.4) |
| Bandar-Abbas | 1 (3.4) |
| Qum | 1 (3.4) |
| Kerman | 1 (3.4) |
| Age | |
| 18–20 | 0 (0.0) |
| 21–30 | 2 (6.9) |
| 31–40 | 17 (58.6) |
| >40 | 10 (34.5) |
| Gender | |
| Men | 18 (62.1) |
| Women | 11 (37.9) |
| Education | |
| High school or below | 25 (86.3) |
| Some college | 1 (3.4) |
| College or above | 3 (10.3) |
| Employment status | |
| Employed | 12 (41.4) |
| Disabled/Retired | 3 (10.3) |
| Unemployed | 14 (48.3) |
| History of drug injection or abuse | |
| Yes | 12 (41.4) |
| No | 17 (58.6) |
| Source of transmission | |
| Sexual behavior | 15 (51.7) |
| Needle or syringe use | 6 (20.7) |
| Blood | 3 (10.3) |
| Unknown | 5 (17.3) |
| Years of living with HIV/AIDS | |
| ≤5 years | 10 (34.5) |
| 6–10 years | 6 (20.7) |
| >10 years | 13 (44.8) |
† Includes current students
Themes and subthemes related to the role of online social networks in improving health literacy and medication adherence of PLWHA.
| Themes | Sub-theme | Example quotes | |
|---|---|---|---|
| Health literacy | Communication support | Improving patient-provider communication | “In this online community, there is a variety of medical specialties including social workers, internal physicians, midwives, and psychologists sharing information with HIV positive patients and answer patients’ questions daily” [Man, 41 years old] |
| Improving peer communication | “We have been friends for 5 years … Here we contact each other in the group for the first time and become very close friends … We are very interdependent and always talk about our smallest to our biggest problems here in the group” [Woman, 35 years old] | ||
| Building trust among users | “Personally, if someone gives me advice about the disease, I do not accept it in the first place. I first try to evaluate whether the source of information is reliable or not …once the quality and credibility of the information is confirmed, I would accept it” [Man, 39 years old] | ||
| Creating collective identity, a sense of belonging and attachment among users | "It’s very valuable to me to see that there is a connection between the patient and that they feel a responsibility to relieve their pain while no one knows where you are from …we are like a family” [Woman, 37 years old] | ||
| Access to information | Enabling remote access to information | “During this period, I think [that] it has helped a lot to those [who are] not able to visit counselling centers or could not remember their questions at the visit time. Since there are some medical staff and physicians in the group; we can ask our questions 24/7. This could particularly help members from other cities to access health professionals and physicians online” [woman, 45 years old] | |
| Maintaining confidentiality and anonymity | “Most members deleted their profile pictures or use anonymous Ids so that nobody can recognize them as HIV positive members” [Man, 39 years old] | ||
| Improving the hidden population’s access to health information | “Many [homeless] guys in Ahwaz rely on me to ask me their questions …I share their questions with doctors in the group and then send the doctor’s advice to my friends reciprocal” [Man, 41 years old] | ||
| Sharing personal experiences/ success stories | Offering interactive Q and A for patients | “At the time I was added to the group, I knew nothing about HIV. By reading other members’ posts and questions/answers shared by physicians, I became aware of complications of the disease and got informed how to deal with them” [Man, 40 years old] | |
| Improving users’ motivations to share personal experiences | “During online interactions among patients, one learns how to express his HIV status instead of hiding it … By presenting ourselves to a group of people without any discrimination or stigma, we are motivated to talk about HIV even among our family or other people” [Man, 38 years old] | ||
| Enhancing observational learning | “In this group, we have different kinds of HIV patients. Some are newly diagnosed patients. Some have been living with HIV for a long time. Some have dealt with the disease successfully but some members are experiencing many challenges. By observing all these patients, one can learn how to manage his situation” [Woman, 39 years old] | ||
| Empowering patients in making a decision | “Communication with other patients in the group helped me identify best practices among my peers and apply them based on my situation.” [Man, 35 years old] | ||
| Creating and maintaining social capital in online communities | “Some members in the group are extremely active, share their personal experiences without any fear … They can affect other members by their thoughts, behaviours and speeches” [Man, 39 years old] | ||
| Increasing knowledge & awareness about HIV | Improving knowledge about symptoms and clinical manifestations of HIV infection | ||
| Improving knowledge about drug benefits/side effects | “I used to be in some patient groups and I didn’t know much about HIV, but now I’m in this group … It is much better … I have learned many new things about HIV including nutrition, drug side effects, herbal drugs, and treatment regimens … [I] asked all my questions or read other members’ questions about HIV … this has increased my knowledge extensively” [Man, 25 years old] | ||
| Providing information about available health services and service providers | “By joining this group and communicating with other patients, I got familiar with health centers near my location that provide services to HIV-positive patients free of charge and deliver health packages for at-risk women and sex-workers” [Woman, 31 years old] | ||
| Enhancing perception &attitudes towards HIV | Enhancing the perception of users about acquiring HIV infection | “Acquiring HIV infection is unbelievable to most people. I denied my HIV-positive test result for months and couldn’t believe that I’d got an HIV infection. By getting involved with other HIV-positive patients, I’ve recognized that the risk of acquiring HIV treats all people irrespective of their sex or socioeconomic class.” [Woman, 32 years old] | |
| Enhancing perception about negative outcomes and severity of the disease | “Most people have misconceptions about HIV/AIDS. They often think that once a person is infected with HIV, he will die in a few years or his mouth will be crooked (for example) or he can no longer get married or have a healthy child” [Woman, 40 years old] | ||
| Enhancing the perception of users about the potential benefits of adapting prevention behaviours | “I’d always thought that HIV-positive patients are not required to use a condom while having sex with each other, but the doctor in the group convinced me that we must use preventive strategies once communicating with other patients rather than healthy people” [Man, 40 years old] | ||
| Improving users’ knowledge about social, personal, environmental, or economic challenges of living with HIV infection | “Losing a job, getting divorced from an HIV-negative wife, and leaving home are frequently reported by HIV-positive members in online groups. Most of my friends experienced such problems after being diagnosed with HIV infection” [Woman, 56 years old] | ||
| Medication adherence | Social support | Facilitating emotional support exchange among users | “Sometimes you need someone thinking about you or you need to feel valuable when you post in a group and then some users like or comment on your post, this simply makes you feel better. When you are in a bad mood or feel depressed, there is someone to talk with you, this makes you feel you are not alone at all. Talking about your disease in a group of peers makes you feel self-confident and powerful” [man, 40 years old] |
| Facilitating instrumental support among users | “In the Kermanshah earthquake, our friends needed help, we collected a lot of help from the group members and sent them … Someone in Kermanshah wanted to commit suicide. We went to Kermanshah and tried to convince her. Now she is an artist and works in the positive club voluntarily” [Man, 35 years old] | ||
| Health-related outcomes | Boosting motivation and self-confidence | “Patients are constantly following other users’ health status and their personal behaviours … They could be inspired and motivated by the success stories of other users and learn from their experiences … Looking at patients who successfully managed the HIV complications improves the motivation and confidence of recently diagnosed patients and encourages them to take an active role in their healthcare management” [Woman, 35 years old] | |
| Improving self-efficacy and self-care behaviours | “While chatting with online patients and looking at their very positive attitude, I’d always felt a twinge of envy for them and wished to be like them … This strong feeling reinforced me to stop drug use and start my ART regimen” [Man, 37 years old] | ||
| Improving medication adherence | “Online communication with other patients in this group offers the opportunity of getting up-to-date information about the disease and becoming aware that what would happen to them if they did not adhere to their medications correctly or interrupted the treatment … It could help non-adherent patients stick to their regimen permanently” [Man, 47 years old] | ||
The consensus rates of items related to the role of OSN technologies in improving health literacy and medication adherence of PLWHA.
| Items | Median | Inter-quartile range | Consensus rate (%) |
|---|---|---|---|
| Improving trust among users | 5 | 1 | 88.4 |
| Facilitating communication between patients and peer groups | 5 | 1 | 96.2 |
| Facilitating communication between patients and health care providers | 5 | 1 | 84.7 |
| Creating identity and a sense of belonging to the group | 5 | 1 | 80.7 |
| Facilitating remote access to information | 5 | 1 | 80.7 |
| Maintaining confidentiality and anonymity of patients in accessing information | 5 | 1 | 92.2 |
| Facilitating access of hidden populations to information | 4 | 1 | 76.8 |
| Promoting interactive Q and A | 5 | 1 | 92.3 |
| Strengthening the motivation of users to share personal experiences | 5 | 1 | 92.3 |
| Facilitating observational learning from the personal experiences of other patients | 5 | 1 | 92.3 |
| Improving patient empowerment and decision making | 5 | 1 | 80.7 |
| Social capital | 4 | 1 | 88.4 |
| Getting familiar with clinical manifestations of the disease | 5 | 1 | 76.9 |
| Getting familiar with the benefits/ side effects of medications | 5 | 1 | 96 |
| Getting familiar with the type of health services and centers providing these services to PLWHA | 5 | 1 | 84.5 |
| Strengthening the sense of vulnerability in patients | 4.5 | 1 | 84.6 |
| Strengthening the patient’s attention to serious complications | 5 | 1 | 80.7 |
| Strengthening the patients’ understanding of the benefits and effectiveness of treatment advice provided by health professionals | 5 | 1 | 92.2 |
| Strengthening the patient’s understanding of barriers to following treatment advice and taking action | 5 | 1 | 80.7 |
| Improving emotional and social support | 5 | 1 | 88.4 |
| Improving instrumental and physical support | 5 | 1 | 76.8 |
| Increasing motivation and self-confidence | 5 | 1 | 88.4 |
| Improving self-efficacy and self-care | 5 | 1 | 88.5 |
| Improving adherence to antiretroviral medications | 5 | 1 | 92.3 |
Fig 1The proposed model of the roles of online social network technologies in improving health literacy and medication adherence of people living with HIV/AIDS.