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Recovery Group Pilot

Recovery Group Pilot

Status
Completed
Phases
NA
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT00522613
Enrollment
50
Registered
2007-08-30
Start date
2005-07-31
Completion date
2006-12-31
Last updated
2009-02-04

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Bipolar Disorder, Schizoaffective Disorder, Schizophrenia

Keywords

recovery, serious mental illness, bipolar disorder, schizophrenia, schizoaffective disorder

Brief summary

The purpose of this study is to develop and evaluate a low-cost, joint consumer/counselor-led, health education and support intervention that will foster self-care and recovery among adults with serious mental illness. Results from the study will indicate how well the workbook and the overall program were received by individuals with serious mental illness, and whether participating in the program appeared to improve recovery and functioning.

Detailed description

Recent research suggests that many individuals with serious mental illnesses may recover from these conditions and become fully integrated into their communities. Although improved medications may be most responsible for these developments, self-help groups, social support, and empowerment have been identified as important facilitators of the recovery process. Recovery-oriented, consumer-led approaches are gaining in popularity, but few of these interventions have been evaluated scientifically. This pilot study proposes to develop and evaluate a recovery-oriented program that centers on the use of a self-help workbook. Results from the study will indicate how well the workbook and the overall program were received by individuals with serious mental illness, and whether participating in the program appeared to improve recovery and functioning. Objectives: 1. To develop group-facilitator materials to complement the self-help workbook. 2. To conduct a randomized trial of the intervention with kaiser Permanente Northwest (KPNW) members with bipolar disorder or schizophrenia/schizoaffective disorder, using a delayed control group design and 6- and 12-month post-intervention follow-up. 3. To assess participant attendance and satisfaction with the group sessions; 4. To assess whether participating in the group intervention was associated with improvements in short-term recovery and functioning.

Interventions

BEHAVIORALRecovery Group Project

Recovery Group Workbook & Group Sessions

Sponsors

Portland State University
CollaboratorOTHER
University of South Florida
CollaboratorOTHER
Kaiser Permanente
Lead SponsorOTHER

Study design

Allocation
RANDOMIZED
Intervention model
PARALLEL
Primary purpose
SUPPORTIVE_CARE
Masking
NONE

Eligibility

Sex/Gender
ALL
Age
18 Years to No maximum
Healthy volunteers
No

Inclusion criteria

* diagnosis of bipolar disorder or schizophrenia/schizoaffective disorder * current membership in KPNW * age 18 or over

Exclusion criteria

* having a guardian * psychotic symptoms that interfere with group interactions * dementia, mental retardation (other than mild) or other organic brain conditions that affect an individual's ability to participate in an interview, a group intervention, or complete questionnaires

Design outcomes

Primary

MeasureTime frame
To develop group-facilitator materials to complement the self-help workbook6 weeks
To conduct a randomized trial of the intervention with KPNW members6 weeks
To assess participant attendance and satisfaction with the group sessions6 weeks
To assess whether participating in the group intervention was associated with improvements in short-term recovery and functioning6 weeks

Countries

United States

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 4, 2026