Individually Based Psychosocial Rehabilitation for Older People With Serious Mental Illness (SMI)
This study is ongoing, but not recruiting participants.
Sponsor:
Dartmouth-Hitchcock Medical Center
Collaborator:
Information provided by (Responsible Party):
Dartmouth-Hitchcock Medical Center
ClinicalTrials.gov Identifier:
NCT00817154
First received: January 5, 2009
Last updated: April 24, 2013
Last verified: April 2013
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Purpose
The major goal of this project is to adapt an existing group-based psychosocial program to enhance community functioning in older people with serious mental illness (SMI). The focus of the adaptation is designing and evaluating an individually based rehabilitative program for older people with SMI who either cannot or choose not to access a group program.
| Condition | Intervention | Phase |
|---|---|---|
|
Schizophrenia Schizoaffective Disorder Bipolar Disorder Major Depression |
Behavioral: HOPES-I |
Phase 1 |
| Study Type: | Interventional |
| Study Design: | Endpoint Classification: Efficacy Study Intervention Model: Single Group Assignment Masking: Open Label Primary Purpose: Health Services Research |
| Official Title: | Individually Based Psychosocial Rehabilitation for Older People With SMI |
Resource links provided by NLM:
MedlinePlus related topics:
Bipolar Disorder
Depression
Mental Disorders
Rehabilitation
Schizophrenia
U.S. FDA Resources
Further study details as provided by Dartmouth-Hitchcock Medical Center:
Primary Outcome Measures:
- To develop an individually based psychosocial rehabilitation program for older adults with SMI. The program will be specified in treatment manuals and will match relevant skills training modules to the functional needs and preferences of consumers. [ Time Frame: baseline, 9 months and 12 months, 15 months ] [ Designated as safety issue: No ]
| Estimated Enrollment: | 40 |
| Study Start Date: | November 2009 |
| Estimated Study Completion Date: | December 2013 |
| Estimated Primary Completion Date: | September 2013 (Final data collection date for primary outcome measure) |
| Arms | Assigned Interventions |
|---|---|
|
Experimental: Hopes-I
The program progresses in three steps. First, participants receive a 10-week Basic Skills for Community Living course covering essential skills from each of the five modules to ensure that all participants establish basic competency in a core set of skills. Second, clinicians assess participants' functioning to identify skill areas that warrant additional improvement and engage participants in a shared decision making process to select skill areas to pursue in greater depth. Third, clinicians have weekly 60 minute sessions with participants in community settings for 7 months to provide training and to facilitate and support acquisition of core skills and rehabilitation goals.
|
Behavioral: HOPES-I
The program progresses in three steps. First, participants receive a 10-week Basic Skills for Community Living course covering essential skills from each of the five modules to ensure that all participants establish basic competency in a core set of skills. Second, clinicians assess participants' functioning to identify skill areas that warrant additional improvement and engage participants in a shared decision making process to select skill areas to pursue in greater depth. Third, clinicians have weekly 60 minute sessions with participants in community settings for 7 months to provide training and to facilitate and support acquisition of core skills and rehabilitation goals.
|
Eligibility| Ages Eligible for Study: | 50 Years and older |
| Genders Eligible for Study: | Both |
| Accepts Healthy Volunteers: | No |
Criteria
Inclusion Criteria:
- Age 50+;
- ability to provide voluntary informed consent or assent, with formal consent by a legal guardian;
- Axis I Disorder of schizophrenia, schizoaffective disorder, bipolar disorder, or major depression;
- Functional impairment based on NH state eligibility criteria for services to people with SMI;
- Enrollment in treatment for at least three months.
Exclusion Criteria:
- residence in a nursing home or assisted living facility;
- Terminal illness expected to result in death within one year or less;
- Diagnosis of dementia, or significant cognitive impairment as indicated by a Mini Mental Status Evaluation (MMSE) score <24;
- Current active substance abuse or dependence;
- Past Participation in HOPES-G
Contacts and Locations
Please refer to this study by its ClinicalTrials.gov identifier: NCT00817154
Locations
| United States, New Hampshire | |
| Riverbend Community Mental Health Center | |
| Concord, New Hampshire, United States, 03301 | |
| Community Council of Nashua | |
| Nashua, New Hampshire, United States, 03060 | |
Sponsors and Collaborators
Dartmouth-Hitchcock Medical Center
Investigators
| Principal Investigator: | Sarah I Pratt, Ph.D. | Dartmouth-Hitchcock Medical Center |
More Information
No publications provided
| Responsible Party: | Dartmouth-Hitchcock Medical Center |
| ClinicalTrials.gov Identifier: | NCT00817154 History of Changes |
| Other Study ID Numbers: | K23MH080021 |
| Study First Received: | January 5, 2009 |
| Last Updated: | April 24, 2013 |
| Health Authority: | United States: Institutional Review Board |
Keywords provided by Dartmouth-Hitchcock Medical Center:
|
Older persons with SMI |
Additional relevant MeSH terms:
|
Bipolar Disorder Depression Depressive Disorder Psychotic Disorders Schizophrenia Depressive Disorder, Major |
Affective Disorders, Psychotic Mood Disorders Mental Disorders Behavioral Symptoms Schizophrenia and Disorders with Psychotic Features |
ClinicalTrials.gov processed this record on May 19, 2013