AMP WellBeing Intervention trial

Not Applicable

Completed

• Conditions: Anxiety and/or depression; Mental and Behavioural Disorders; Anxiety disorder, unspecified

• Registration Number: ISRCTN68572159
• Lead Sponsor: niversity of Liverpool (UK)

Brief Summary

Not available

Detailed Description

Not available

Study Timeline

• Study Start: 2013-02-25
• Last Update Posted: 7 November 2016

Recruitment & Eligibility

• Status: Completed
• Sex: All
• Target Recruitment: 100

Inclusion Criteria

1. Male and female aged 50 and over for Croxteth and Wythenshawe participants
2. Aged 18 and over for Picton and Longsight participants
3. Somali heritage in Picton and South Asian (Pakistani or Bangladeshi) in Longsight; registered with one of the 16 primary care practices working with the AMP Development Partnership
4. Scoring 10 or more on the Patient Health Questionnaire 9 (PHQ)-9 and/or the Generalized Anxiety Disorder 7 (GAD-7)

Exclusion Criteria

1. Currently deemed to be at significant risk to themselves or others
2. Significant learning disabilities and cognitive impairment

Study & Design

• Study Type: Interventional
• Study Design: Not specified

Primary Outcome Measures

Name	Time	Method
CORE-OM, a 34-item self report scale designed to measure global distress, including subjective well being, life/social functioning and risk measured at baseline and 20 weeks

Secondary Outcome Measures

Name	Time	Method
1. PHQ-9 for depression<br>2. GAD-7 for anxiety<br>3. The Work and Social Adjustment Scale <br>4. The EQ-5D for quality of life<br>Measured at baseline and 20 weeks