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OpenTrials
Completed

NCT Number: NCT00522613

Recovery Group Pilot

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.

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Key information

Age range

18 year and older

Sex eligibility

All sexes

Study type

Interventional

Phase

Not applicable

Primary location

Kaiser Permanente Center for Health Research

Portland, Oregon, 97227, United States

About this study

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:

  • To develop group-facilitator materials to complement the self-help workbook.
  • 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.
  • To assess participant attendance and satisfaction with the group sessions;
  • To assess whether participating in the group intervention was associated with improvements in short-term recovery and functioning.

Who can participate

Healthy volunteers accepted: No

Only the study team can determine whether someone qualifies for participation.

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

Treatment and study plan

Recovery Group Project

Behavioral

Recovery Group Workbook & Group Sessions

Primary outcomes

  1. To develop group-facilitator materials to complement the self-help workbook

    Time frame: 6 weeks

  2. To conduct a randomized trial of the intervention with KPNW members

    Time frame: 6 weeks

  3. To assess participant attendance and satisfaction with the group sessions

    Time frame: 6 weeks

  4. To assess whether participating in the group intervention was associated with improvements in short-term recovery and functioning

    Time frame: 6 weeks

Sponsors and collaborators

Lead sponsor

Kaiser Permanente

Other

Collaborators

  • Portland State University
  • University of South Florida

Registry information

Important dates

Study start
2005
Primary completion
2006
Study completion
2006
First posted
Aug 30, 2007
Registry last updated
Feb 4, 2009

OpenTrials presents study information sourced from ClinicalTrials.gov. The official registry record should be consulted for the latest information.

View the official ClinicalTrials.gov record (opens in a new tab)

This listing is for discovery and informational purposes only. It is not medical advice, does not guarantee that a study is recruiting, and does not determine eligibility. Contact the study team and a qualified healthcare professional when considering participation.

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