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Clinical Trial Details — Status: Completed

Administrative data

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

Study information

Verified date May 2018
Source Université de Montréal
Contact n/a
Is FDA regulated No
Health authority
Study type Interventional

Clinical Trial Summary

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.


Description:

This study was a three-arm pilot randomized control trial with mixed methods. Participants were randomized to PMR, AT, or control group (CG), with four assessments (baseline, one-, three-, and six-month). The PMR and AT interventions consisted of six one-hour sessions of individual training over 12 weeks and home practice. Recruitment, attrition, and completion rates were calculated. Depressive symptoms and quality of life were assessed at all times. Participants' perceptions of the interventions were collected in semi-structured interviews.


Recruitment information / eligibility

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

Study Design


Related Conditions & MeSH terms


Intervention

Behavioral:
Jacobson progressive muscular relaxation
PMR involves learning to identify the tension in specific muscle groups by tightening and relaxing each muscle group. It includes three different exercises: 1) contraction-relaxation of 12 large muscle groups in the arms, legs, and trunk; 2) identification and relaxation of tensions without the need for movement or contractions; and 3) contraction-relaxation of 12 small muscle groups in the neck, eyes, and mouth
Schultz's autogenic training
AT is a relaxation technique that is based on body attitude, reduction of exterior stimulation, inner concentration, and mental repetition of verbal formulas [28]. These formulas are organized into six exercises: 1) heaviness; 2) warmth; 3) calm and regular heart function; 4) self-regulation of respiration; 5) warmth in the upper abdominal area; and 6) agreeable cooling of the forehead.

Locations

Country Name City State
Canada Research center CHUM Montréal Quebec

Sponsors (3)

Lead Sponsor Collaborator
Université de Montréal Laval University, RRISIQ

Country where clinical trial is conducted

Canada, 

Outcome

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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