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NCT02481713 Clinical Trial

Improving Adherence to Cognitive Rehabilitation

Psychosis Clinical Trial

Official title:
Enhancing Adherence to Cognitive Rehabilitation

Clinical Trial Details — Status: Completed

Administrative data
NCT number NCT02481713
Other study ID # D1790-R
Secondary ID
Status Completed
Phase N/A
First received
Last updated
Start date December 1, 2015
Est. completion date September 30, 2020

Study information
Verified date October 2021
Source VA Office of Research and Development
Contact n/a
Is FDA regulated No
Health authority
Study type Interventional

Clinical Trial Summary

Purpose of study is to evaluate impact of brief motivational interviewing vs. feedback on learning styles in improving attendance to cognitive training

Description:

This study is evaluating whether motivational enhancement can improve outcomes of cognitive rehabilitation in Veterans with schizophrenia spectrum disorders. Approximately 120 individuals will be randomized to either a 2-session motivational interview (MI, experimental condition) or a 2-session assessment and feedback on learning styles (CI, active control), and will then be asked to participate in 4 months of cognitive rehabilitation. Booster MI or CI sessions will be administered monthly over the course of the cognitive rehabilitation. Primary outcome is number of cognitive rehabilitation sessions attended.

Recruitment information / eligibility
Status Completed
Enrollment 114
Est. completion date September 30, 2020
Est. primary completion date September 30, 2020
Accepts healthy volunteers No
Gender All
Age group 18 Years and older
Eligibility Inclusion Criteria: - diagnosis of psychotic disorder - 18 years old or older Exclusion Criteria: - meeting criteria for substance abuse/dependence in past 30 days - psychiatric hospitalization in past 30 days - change in psychiatric medications in past 30 days - severe auditory/visual impairment - evidence of developmental disability

Study Design

Related Conditions & MeSH terms

Intervention

Behavioral:
• motivational interviewing
motivational interviewing
• learning style interviews
interview and feedback about learning style

Locations
Country Name City State
United States VA Connecticut Healthcare System West Haven Campus, West Haven, CT West Haven Connecticut

Sponsors (1)
Lead Sponsor Collaborator
VA Office of Research and Development

Country where clinical trial is conducted

United States, 

Outcome
Type Measure Description Time frame Safety issue
Primary Number of Sessions Attended number of cognitive training sessions attended end of four month training period
Primary Number of Sessions Attended number of sessions attended among patients who attended at least 1 session end of 4 month training period
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