Group Cognitive Behavioral Therapy (CBT) Intervention for Women With Mild to Moderate Depression

The purpose of this study is to develop a structured CBT group intervention for women with depression of mild or moderate severity and to pilot a randomized controlled trial to compare this intervention with usual care in socially deprived areas in Bristol, incorporating qualitative methods to assess acceptability.

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Key information

Conditions

Depression Anxiety Anxiety Disorders Behavior Behavioral Symptoms Mental Disorders

Age range

30 year–54 year

Sex eligibility

Female

Study type

Interventional

Phase

Early Phase 1

Primary location

Wellspring Healthy Living Centre, Bristol, United Kingdom

Who can participate

Healthy volunteers accepted: No

Only the study team can determine whether someone qualifies for participation.

Inclusion criteria

mild to moderate depression
antidepressant use is also OK

Exclusion criteria

able to speak english
abusing drugs or alcohol
using secondary mental health services

Treatment and study plan

Brief CBT Group therapy

Behavioral

CBT based therapy also expert patient programme

Primary outcomes

PHQ-9 Score

Time frame: 3 months and 6 months

Sponsors and collaborators

Lead sponsor

University of Bristol

Other

Registry information

Official study title

A Pilot Study to Develop a Brief Group Intervention for Women With Mild and Moderate Depression

Acronym: BackonTrack

Important dates

Study start: 2007
Primary completion: 2009
Study completion: 2009
First posted: Apr 22, 2008
Registry last updated: Jan 14, 2010

OpenTrials presents study information sourced from ClinicalTrials.gov. The official registry record should be consulted for the latest information.

View the official ClinicalTrials.gov record (opens in a new tab)

This listing is for discovery and informational purposes only. It is not medical advice, does not guarantee that a study is recruiting, and does not determine eligibility. Contact the study team and a qualified healthcare professional when considering participation.

Published trials that share one or more normalized conditions with this study.

Completed