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Clinical Trial Details — Status: Withdrawn

Administrative data

NCT number NCT05584215
Other study ID # 12462
Secondary ID
Status Withdrawn
Phase N/A
First received
Last updated
Start date June 3, 2023
Est. completion date January 2, 2024

Study information

Verified date March 2024
Source Lawson Health Research Institute
Contact n/a
Is FDA regulated No
Health authority
Study type Interventional

Clinical Trial Summary

This is a feasibility study of cognitive behavioural therapy-informed groups for psychiatric inpatients with positive symptoms of psychosis.


Description:

The majority of inpatients at Parkwood Institute Mental Health have symptoms of psychosis. In line with Health Quality Ontario standards for the treatment of psychosis, the investigators would like to implement and evaluate cognitive behavioural therapy for psychosis (CBTp) informed groups. The feasibility, acceptability, and preliminary efficacy of CBTp groups for inpatients will be examined. Pragmatically, the investigators propose to undergo training in CBTp, implement empirically-supported CBTp protocols developed for inpatients, track outcomes, and publish our findings. The investigators would also incorporate patient feedback to improve future iterations of the protocol. Such an undertaking would build research capacity in front line staff by encouraging engagement in CBTp group training, survey design, participant screening, data collection, analyses, and dissemination of findings.


Recruitment information / eligibility

Status Withdrawn
Enrollment 0
Est. completion date January 2, 2024
Est. primary completion date January 2, 2024
Accepts healthy volunteers No
Gender All
Age group 18 Years to 65 Years
Eligibility Inclusion Criteria: - Can read/write in English - Has positive symptoms of psychosis that are distressing to them Exclusion Criteria: - Inability to tolerate group participation

Study Design


Related Conditions & MeSH terms


Intervention

Behavioral:
Cognitive Behavioural Therapy for Psychosis Groups
Groups based on cognitive behavioural therapy for psychosis

Locations

Country Name City State
n/a

Sponsors (1)

Lead Sponsor Collaborator
Lawson Health Research Institute

Outcome

Type Measure Description Time frame Safety issue
Other Satisfaction Questionnaire Brief open-ended questions about program satisfaction. Responses are qualitative. Up to 2 months
Primary Clinical Outcomes in Routine Evaluation 10 (CORE-10) The Clinical Outcomes in Routine Evaluation 10 is a short 10 item easy-to-use assessment measure for common presentations of psychological distress, designed to be used for screening as well as over the course of treatment to track progress. The minimum value is 0, the maximum value is 40, and higher scores indicate a worse outcome. Up to 2 months
Primary Process of Recovery Questionnaire (QPR) The Process of Recovery Questionnaire is a 15 item questionnaire which was co-produced by people who experience psychosis and their accounts of recovery. The minimum value is 0, the maximum value is 60, and higher scores indicate a better outcome. Up to 2 months
Secondary The Positive and Negative Syndrome Scale (PANSS) - Positive Symptoms A brief measure of positive symptoms of psychosis. The minimum value is 7, the maximum values is 49. Higher scores indicate a worse outcome. Up to 2 months
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