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Problem Management Plus (PM+) in the management of common mental disorders in a specialized mental healthcare facility in Pakistan; study protocol for a randomized controlled trial

BACKGROUND: The World Health Organization (WHO) has developed Problem Management Plus (PM+), a 5-session, psychological intervention program delivered by trained non-specialist that addresses common mental disorders. The objectives of this study are to evaluate effectiveness and cost-effectiveness o...

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Autores principales: Hamdani, Syed Usman, Ahmed, Zainab, Sijbrandij, Marit, Nazir, Huma, Masood, Aqsa, Akhtar, Parveen, Amin, Hania, Bryant, Richard A., Dawson, Katie, van Ommeren, Mark, Rahman, Atif, Minhas, Fareed Aslam
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2017
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5465445/
https://www.ncbi.nlm.nih.gov/pubmed/28603552
http://dx.doi.org/10.1186/s13033-017-0147-1
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author Hamdani, Syed Usman
Ahmed, Zainab
Sijbrandij, Marit
Nazir, Huma
Masood, Aqsa
Akhtar, Parveen
Amin, Hania
Bryant, Richard A.
Dawson, Katie
van Ommeren, Mark
Rahman, Atif
Minhas, Fareed Aslam
author_facet Hamdani, Syed Usman
Ahmed, Zainab
Sijbrandij, Marit
Nazir, Huma
Masood, Aqsa
Akhtar, Parveen
Amin, Hania
Bryant, Richard A.
Dawson, Katie
van Ommeren, Mark
Rahman, Atif
Minhas, Fareed Aslam
author_sort Hamdani, Syed Usman
collection PubMed
description BACKGROUND: The World Health Organization (WHO) has developed Problem Management Plus (PM+), a 5-session, psychological intervention program delivered by trained non-specialist that addresses common mental disorders. The objectives of this study are to evaluate effectiveness and cost-effectiveness of PM+ in a specialized mental health care facility in Pakistan. METHODS: A single blind individual randomized controlled trial (RCT) will be carried out in the outpatient department of a specialized mental healthcare facility in Rawalpindi, Pakistan. After informed consent, patients with high psychological distress (General Health Questionnaire-12 (score >2) and functional impairment (WHO Disability Assessment Schedule 2.0 score >16) will be randomised to PM+ plus treatment as usual (n = 96) or TAU only (n = 96). The primary outcome is the psychological distress, measured by levels of anxiety and depression on the Hospital Anxiety and Depression Scale and improvement in functioning as measured by WHODAS at 20 weeks after baseline. Secondary outcomes include improvement in symptoms of depression, post-traumatic stress disorder, levels of social support and cost effectiveness evaluation. Qualitative interviews will be conducted to evaluate the process of implementing PM+ including barriers and facilitators in implementation and possibility of integration of PM+ program in specialized mental health care facilities in Pakistan. DISCUSSION: The results of this study will be helpful in evaluating the effectiveness of the approach of training non specialists, based in the specialized mental health care facilities in delivering evidence based psychological interventions in the low resource settings. Trial registration Australian New Zealand Clinical Trials Registry, ACTRN12616000381482. Registered Retrospectively on March 23, 2016 ELECTRONIC SUPPLEMENTARY MATERIAL: The online version of this article (doi:10.1186/s13033-017-0147-1) contains supplementary material, which is available to authorized users.
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spelling pubmed-54654452017-06-09 Problem Management Plus (PM+) in the management of common mental disorders in a specialized mental healthcare facility in Pakistan; study protocol for a randomized controlled trial Hamdani, Syed Usman Ahmed, Zainab Sijbrandij, Marit Nazir, Huma Masood, Aqsa Akhtar, Parveen Amin, Hania Bryant, Richard A. Dawson, Katie van Ommeren, Mark Rahman, Atif Minhas, Fareed Aslam Int J Ment Health Syst Study Protocol BACKGROUND: The World Health Organization (WHO) has developed Problem Management Plus (PM+), a 5-session, psychological intervention program delivered by trained non-specialist that addresses common mental disorders. The objectives of this study are to evaluate effectiveness and cost-effectiveness of PM+ in a specialized mental health care facility in Pakistan. METHODS: A single blind individual randomized controlled trial (RCT) will be carried out in the outpatient department of a specialized mental healthcare facility in Rawalpindi, Pakistan. After informed consent, patients with high psychological distress (General Health Questionnaire-12 (score >2) and functional impairment (WHO Disability Assessment Schedule 2.0 score >16) will be randomised to PM+ plus treatment as usual (n = 96) or TAU only (n = 96). The primary outcome is the psychological distress, measured by levels of anxiety and depression on the Hospital Anxiety and Depression Scale and improvement in functioning as measured by WHODAS at 20 weeks after baseline. Secondary outcomes include improvement in symptoms of depression, post-traumatic stress disorder, levels of social support and cost effectiveness evaluation. Qualitative interviews will be conducted to evaluate the process of implementing PM+ including barriers and facilitators in implementation and possibility of integration of PM+ program in specialized mental health care facilities in Pakistan. DISCUSSION: The results of this study will be helpful in evaluating the effectiveness of the approach of training non specialists, based in the specialized mental health care facilities in delivering evidence based psychological interventions in the low resource settings. Trial registration Australian New Zealand Clinical Trials Registry, ACTRN12616000381482. Registered Retrospectively on March 23, 2016 ELECTRONIC SUPPLEMENTARY MATERIAL: The online version of this article (doi:10.1186/s13033-017-0147-1) contains supplementary material, which is available to authorized users. BioMed Central 2017-06-08 /pmc/articles/PMC5465445/ /pubmed/28603552 http://dx.doi.org/10.1186/s13033-017-0147-1 Text en © The Author(s) 2017 Open AccessThis article is distributed under the terms of the Creative Commons Attribution 4.0 International License (http://creativecommons.org/licenses/by/4.0/), which permits unrestricted use, distribution, and reproduction in any medium, provided you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons license, and indicate if changes were made. The Creative Commons Public Domain Dedication waiver (http://creativecommons.org/publicdomain/zero/1.0/) applies to the data made available in this article, unless otherwise stated.
spellingShingle Study Protocol
Hamdani, Syed Usman
Ahmed, Zainab
Sijbrandij, Marit
Nazir, Huma
Masood, Aqsa
Akhtar, Parveen
Amin, Hania
Bryant, Richard A.
Dawson, Katie
van Ommeren, Mark
Rahman, Atif
Minhas, Fareed Aslam
Problem Management Plus (PM+) in the management of common mental disorders in a specialized mental healthcare facility in Pakistan; study protocol for a randomized controlled trial
title Problem Management Plus (PM+) in the management of common mental disorders in a specialized mental healthcare facility in Pakistan; study protocol for a randomized controlled trial
title_full Problem Management Plus (PM+) in the management of common mental disorders in a specialized mental healthcare facility in Pakistan; study protocol for a randomized controlled trial
title_fullStr Problem Management Plus (PM+) in the management of common mental disorders in a specialized mental healthcare facility in Pakistan; study protocol for a randomized controlled trial
title_full_unstemmed Problem Management Plus (PM+) in the management of common mental disorders in a specialized mental healthcare facility in Pakistan; study protocol for a randomized controlled trial
title_short Problem Management Plus (PM+) in the management of common mental disorders in a specialized mental healthcare facility in Pakistan; study protocol for a randomized controlled trial
title_sort problem management plus (pm+) in the management of common mental disorders in a specialized mental healthcare facility in pakistan; study protocol for a randomized controlled trial
topic Study Protocol
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5465445/
https://www.ncbi.nlm.nih.gov/pubmed/28603552
http://dx.doi.org/10.1186/s13033-017-0147-1
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