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Clinical Trial Details — Status: Completed

Administrative data

NCT number NCT03499548
Other study ID # 238927
Secondary ID
Status Completed
Phase N/A
First received
Last updated
Start date June 1, 2018
Est. completion date April 26, 2019

Study information

Verified date August 2019
Source University of Manchester
Contact n/a
Is FDA regulated No
Health authority
Study type Interventional

Clinical Trial Summary

This study aims to assess the acceptability and feasibility of a short-term, intensive Cognitive Behavioural Therapy (CBT) delivered to male prisoners who have thoughts of ending their lives.


Description:

10 hours of an adapted CBT therapy for suicide will be delivered across 2 weeks in 5 2 hour sessions to male prisoners. They will initially be assessed on several measures of mood, social support and suicidality. They will then undergo therapy. Following this they will be asked to re-completed the initial measures and a post-therapy interview to ascertain their thoughts on their experience of the therapy.


Recruitment information / eligibility

Status Completed
Enrollment 13
Est. completion date April 26, 2019
Est. primary completion date April 26, 2019
Accepts healthy volunteers No
Gender Male
Age group 21 Years and older
Eligibility Inclusion Criteria:

- Aged over 21 years old.

- Has been managed under the Assessment, Care in Custody, and Teamwork (ACCT) system within the last 1 month (including current ACCT review).

- Sufficient English language proficiency, as judged by the researcher, in order to complete psychometric questionnaires (i.e. adequate reading comprehension) and engage in intensive CBT programme (i.e. adequate verbal communication).

- Adult is able to provide informed consent as established during baseline clinical interview (BPS, 2006; MCA, 2005).

- Currently residing in HM Prison (and expected to remain there for at least six weeks; determined through staff and prisoner report).

Exclusion Criteria:

- A primary organic disorder (indicated by prison medical staff report or records).

- Any current risk behaviour which would compromise the safety of others, as identified by prison staff.

Study Design


Related Conditions & MeSH terms


Intervention

Other:
INSPiRe Programme
Intensive CBT for suicide

Locations

Country Name City State
United Kingdom HMP Risley Warrington Greater Manchester

Sponsors (1)

Lead Sponsor Collaborator
University of Manchester

Country where clinical trial is conducted

United Kingdom, 

Outcome

Type Measure Description Time frame Safety issue
Primary The Client Satisfaction Questionnaire (CSQ-8) A measure of participant satisfaction with therapy 20 minutes
Primary Therapist Session Summary Measuring levels of adherence and engagement 5 minutes
Primary Discharge summary sheet Capturing individuals' adherence to the programme or discharge from it 15 minutes
Primary Therapist Rating Form Giving an overall picture of each individual's engagement and progress during the study. 20 minutes
Primary Post-intervention interview Qualitative interview to explore the participant's experience of therapy 1 hour
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