HIV Clinical Trial
Official title:
Relaxation, Depressive Symptoms, Quality of Life, Immunological and Virological Status o in People Living With HIV: a Pilot Study
NCT number | NCT01901016 |
Other study ID # | RELHIV-13 |
Secondary ID | |
Status | Completed |
Phase | N/A |
First received | |
Last updated | |
Start date | June 2013 |
Est. completion date | December 2015 |
Verified date | May 2018 |
Source | Université de Montréal |
Contact | n/a |
Is FDA regulated | No |
Health authority | |
Study type | Interventional |
Progressive muscle relaxation (PMR) and autogenic training (AT) are effective relaxation techniques to reduce depressive symptoms. However, no studies on their effectiveness have been conducted among people living with HIV and depressive symptoms. The primary aim of this pilot study was to assess the feasibility and acceptability of PMR and AT interventions among people living with HIV who have depressive symptoms. A secondary aim was to assess the potential effectiveness of these interventions on depressive symptoms and quality of life.
Status | Completed |
Enrollment | 42 |
Est. completion date | December 2015 |
Est. primary completion date | September 2015 |
Accepts healthy volunteers | No |
Gender | All |
Age group | 18 Years and older |
Eligibility | Inclusion Criteria: - Age > 18 years - HIV diagnosis of at least two years - Depressive symptoms between 5 and 14 in the PHQ-9 scale - Untreated with antidepressants or psychotherapy - Able to speak and understand French Exclusion Criteria: - Started antiretroviral treatment within the last 6 months - Start or already receiving Interferon |
Country | Name | City | State |
---|---|---|---|
Canada | Research center CHUM | Montréal | Quebec |
Lead Sponsor | Collaborator |
---|---|
Université de Montréal | Laval University, RRISIQ |
Canada,
Type | Measure | Description | Time frame | Safety issue |
---|---|---|---|---|
Other | Change from baseline in viral load assessed at 6 months | Change from baseline in viral load assessed at 6 months | baseline and 6 months | |
Other | Change from baseline in CD4+ T cells count at 6 months | Change from baseline in CD4+ T cells count at 6 months | baseline and 6 months | |
Primary | Change from baseline in depressive symptoms measured with Personal Health Questionnaire (PHQ-9) assessed at 3 months | Depressive symptoms at 3 months will be measured with Personal Health Questionnaire (PHQ-9) | baseline and 3 months | |
Primary | Change from baseline in depressive symptoms measured with Personal Health Questionnaire (PHQ-9) assessed at 6 months | Depressive symptoms at 6 months will be measured with Personal Health Questionnaire (PHQ-9) | baseline and 6 months | |
Primary | Change from baseline in depressive symptoms measured with Personal Health Questionnaire (PHQ-9)assessed at 1 month | Depressive symptoms at 1 month will be measured with Personal Health Questionnaire (PHQ-9) | baseline and 1 month | |
Secondary | Change from baseline in quality of life measured with (MOS-HIV) Medical Outcome Study-HIV assessed at 6 months | Quality of life at 6 months will be measured with MOS-HIV) Medical Outcome Study-HIV | baseline and 6 months | |
Secondary | Change from baseline in quality of life measured with MOS-HIV) Medical Outcome Study-HIV assessed at 3 months | Quality of life at 3 months will be measured with MOS-HIV) Medical Outcome Study-HIV | baseline and 3 months |
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