Viewing Study NCT00375167



Ignite Creation Date: 2024-05-05 @ 5:03 PM
Last Modification Date: 2024-10-26 @ 9:27 AM
Study NCT ID: NCT00375167
Status: COMPLETED
Last Update Posted: 2019-03-06
First Post: 2006-09-11

Brief Title: Efficacy of the Recovery Workbook as a Psychoeducational Tool for Facilitating Recovery
Sponsor: Queens University
Organization: Queens University

Study Overview

Official Title: Efficacy of the Recovery Workbook as a Psychoeducational Tool for Facilitating Recovery in Persons With Severe and Persistent Mental Illness
Status: COMPLETED
Status Verified Date: 2018-11
Last Known Status: None
Delayed Posting: No
If Stopped, Why?: Not Stopped
Has Expanded Access: False
If Expanded Access, NCT#: N/A
Has Expanded Access, NCT# Status: N/A
Acronym: None
Brief Summary: The present study will determine if Spaniol and colleagues 1994 Recovery Workbook group intervention is an effective clinical tool to move a person with SMI along in their journey of recovery The primary outcome measurements of this study will be the participants perceived level of empowerment hope and optimism knowledge of recovery and life satisfaction This kind of information would add to the current body of knowledge about how principles of recovery can be used in psychoeducational programs used by outpatient community mental health services
Detailed Description: ABSTRACT

Objective Adopting the principles of recovery into the mental health field has been a growing area for discussion at many different levels of care The present study will determine if Spaniol and colleagues 1994 Recovery Workbook group intervention can be used as an effective clinical tool to move a person with a severe mental illness along in their journey of recovery The primary outcome measurements of this study will be the participants perceived level of empowerment hope and optimism knowledge of recovery and life satisfaction Method The study will be a multicenter prospective single-blinded randomized control trial Sixty participants will be recruited from three Assertive Community Treatment Teams ACTT in Kingston Ontario and individuals will be randomized to either the control or intervention arm of the study The control arm of the study will receive their regular services from ACTT The intervention arm will participate in a 10-week psychoeducational group program in addition to receiving their regular services from ACTT Results Analysis will be performed by intention to treat based on total scores of four assessments which will be performed at the trial commencement and termination

Study Oversight

Has Oversight DMC: None
Is a FDA Regulated Drug?: None
Is a FDA Regulated Device?: None
Is an Unapproved Device?: None
Is a PPSD?: None
Is a US Export?: None
Is an FDA AA801 Violation?: None