Medication Adherence Clinical Trial
Official title:
Acceptability, Feasibility and Effectiveness of a Mindfulness Based Intervention to Promote Adherence to Antiretroviral Therapy Among Adolescents in Kampala.
Verified date | May 2023 |
Source | Infectious Diseases Research Collaboration, Uganda |
Contact | n/a |
Is FDA regulated | No |
Health authority | |
Study type | Interventional |
Adolescents represent a growing share of people living with HIV in sub-Saharan Africa (SSA), yet show poor adherence to medication and viral suppression (VS) compared to adults. Investigators postulate that to achieve optimal adherence, support interventions that resonate with life-stages changes in adolescence need to be tested and promoted. Mindfulness and acceptance based interventions are slowly gaining traction as appropriate for adolescents. The study proposes to explore acceptability of an adapted mindfulness and acceptance-based psychosocial intervention (acceptance and commitment therapy: Discoverer, Noticer, Advisor-values model-ACT-DNA-v), among providers (health care practitioners -HCPs) and users (adolescents living with HIV/AIDS-ALWHA). Further, it endeavors to measure feasibility and effectiveness of ACT-DNA-v in reducing psychological barriers to adherence among ALWHAs. The study is to be conducted at two public health centers in Kampala-Uganda. The study design is exploratory sequential mixed-methods; where qualitative data is to be used to explore acceptance of ACT-DNA-v, while quantitative data will be used to measure feasibility of the intervention and its effectiveness in reducing psychosocial barriers to adherence. Qualitative exploratory methods will guide exploration of acceptability of ACT-DNA-v among users and providers; collecting data with a semi-structured interview on domains of inquiry including; understanding, satisfaction, intention to use and perceived appropriateness of ACT-DNA-v. A randomized control trial with quantitative surveys at baseline, post-intervention and follow-up will used to measure the effects of the intervention on process and clinical outcomes among ALWHA. Thematic data analysis will be used to analyze qualitative data, while T-test, Wilcoxon rank sum test, Fisher's exact and Chi-square tests respectively will be used to ascertain average mean differences between the ACT group and the control group on the outcome parameters.
Status | Completed |
Enrollment | 122 |
Est. completion date | June 15, 2023 |
Est. primary completion date | June 15, 2023 |
Accepts healthy volunteers | No |
Gender | All |
Age group | 15 Years to 19 Years |
Eligibility | Inclusion Criteria: - Participant should be 15-19 years of age. - Diagnosed HIV positive. - Attending care at the two study sites (Kisenyi and Kitebi) for the last 6 months. - On first or second line of treatment. - Can speak/understand Luganda or English. - Willing to provide informed consent/assent. - All records will be confirmed via clinic medical charts. Exclusion Criteria: - A participant plan to move out of the catchment area within six months. - Participant is participating in another study related to HIV and care improvement. |
Country | Name | City | State |
---|---|---|---|
Uganda | Kisenyi Health center iv | Kampala | Central Region |
Uganda | Kitebi health center iii | Kampala | Non-US/Non-Canadian |
Lead Sponsor | Collaborator |
---|---|
Infectious Diseases Research Collaboration, Uganda | Fogarty International Center of the National Institute of Health, Makerere University, National Institutes of Health (NIH) |
Uganda,
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Type | Measure | Description | Time frame | Safety issue |
---|---|---|---|---|
Other | Psychological flexibility; measured by the Avoidance and Fusion Questionnaire for youths (AFQ-Y8). | This is a process measure and mechanism of change. AFQ-Y8 measures cognitive fusion and experiential avoidance as impediments to attaining Psychological Flexibility. Scores of the AFQ-Y8 range from 0-24, with higher scores indicating higher levels of psychological inflexibility. The outcome measure for Psychological flexibility will be the number of participants in a given study arm reporting change from baseline psychological inflexibility at post intervention and at three months follow-up as assessed by the AFQ-Y8. | At three months | |
Primary | Change in levels of Depression; measured by Beck's Depression Inventory-ii | The outcome measure will be; number of participants in a given study group reporting change from baseline depression levels at post intervention and after three months follow-up. The change will be assessed by Beck's depression inventory-ii. According to the BDI-ii, scores in the range of 0-13 represent minimal depression, 14-19 mild depression, 20-28 moderate, while 29-63 severe depression. | pre-intervention and at four weeks post intervention assessment | |
Primary | Change in Health related anxiety; measured by the short health anxiety inventory | The outcome measure will be number of participants in a given study arm reporting change from baseline health anxiety at post intervention and at three months follow-up. According to the SHAI, 40.5 is the cut-off score separating clinical and non-clinical health related anxiety. | At pre-intervention and at four weeks post intervention assessment | |
Primary | Change in AIDS related Internalized stigma; measured by Internalized AIDS related stigma scale (IARSS-6) | After dichotomizing the IARSS-6 at median value (0-2 & 3-6), two categories will be created. Category 1 is in the 0-2 range (representing low-moderate stigma) while category 2 is the 3-6 range (representing higher experience of stigma). The measure will then be; the number of participants in a given study arm reporting change from baseline AIDS related stigma at post intervention and at three months follow-up as assessed by the internalized AIDS related stigma scale. | At pre-intervention and at four weeks post intervention assessment | |
Secondary | Self-reported medication adherence; measured by the Morisky Medication Adherence scale-MMAS-8. | The 3 categorical Likert Scale is low adherence = <6, medium adherence = 6-<8 and high adherence is = 8. | At three months | |
Secondary | Viral load | This measure will be based on clinic records. Viral load measures (copies/milliliter of blood) for each participant in both groups will be recorded at baseline and at follow-up. A comparison will be made to detect if there is a difference at time points and across groups. | At three months |
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