A mixed-method randomized feasibility trial evaluating progressive muscle relaxation or autogenic training on depressive symptoms and quality of life in people living with human immunodeficiency virus (HIV) who have depressive symptoms

Author:

Ramirez-Garcia Maria Pilar123ORCID,Leclerc-Loiselle Jérôme45ORCID,Gagnon Marie-Pierre635,Côté José453,Brouillette Marie-Josée78,Thomas Réjean98

Affiliation:

1. Faculty of Nursing , Université de Montréal , Montréal , Quebec , Canada

2. Research Center of the Centre Hospitalier de l' , Université de Montréal , Montréal , Quebec , Canada

3. Quebec Nursing Intervention Research Network (RRISIQ) , Quebec , Canada

4. Faculté des sciences infirmières , Université de Montréal , Montréal , Quebec , Canada

5. Centre de recherche du CHUM , Montréal , Quebec , Canada

6. Faculté des Sciences Infirmières de l'Université Laval , Quebec , Canada

7. Department of Psychiatry , McGill University , Montréal , Quebec , Canada

8. AIDS and Infectious Disease Network (SIDA-MI) , Quebec , Canada

9. Clinique médicale l'Actuel , Montréal , Quebec , Canada

Abstract

Abstract Background 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. Methods This study was a three-arm pilot randomized control trial with mixed methods. Participants were randomized to PMR, AT, or a control group (CG), with four assessments (baseline, and at one, three, and six months). The PMR and AT interventions consisted of six 1 h sessions of individual training over 12 weeks, plus 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. Results Following the screening, 54/63 people met the inclusion criteria, and 42/54 were randomly allocated to the PMR group (n=14), AT group (n=14), and CG (n=14). Six participants (43%; 95% CI 18–71%) in the PMR group and 10 (71%; 95% CI 42–92%) in the AT group completed the intervention. Participants reported better emotion management and improvements in depressive symptoms and quality of life. Conclusions The pilot study suggests that a randomized trial to test the effectiveness of these interventions is feasible. Trial registration ClinicalTrials.gov NCT01901016

Funder

Université Laval – Faculty of Nursing

Quebec Nursing Intervention Research Network, Université Laval

Canadian Institutes of Health Research

Publisher

Walter de Gruyter GmbH

Subject

Complementary and alternative medicine

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