A Self-Management Program for Adults With Both Schizophrenia and a Co-Occurring Medical Condition
Recruitment status was Recruiting
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Purpose
This study will develop and evaluate the effectiveness of a self-management program for adults living with both schizophrenia and a co-occurring medical condition.
| Condition | Intervention |
|---|---|
|
Schizophrenia |
Behavioral: Self-management program for chronic illness |
| Study Type: | Interventional |
| Study Design: | Allocation: Randomized Endpoint Classification: Efficacy Study Intervention Model: Parallel Assignment Masking: Open Label Primary Purpose: Supportive Care |
| Official Title: | Optimizing Chronic Illness Self-Management for Individuals With Schizophrenia |
- Health-related self-efficacy and recovery orientation [ Time Frame: Measured at pre- and post-intervention ] [ Designated as safety issue: No ]
- Medical illness self-management skills [ Time Frame: Measured at pre- and post-intervention ] [ Designated as safety issue: No ]
- Social and communication skills during interactions with health care providers [ Time Frame: Measured at pre- and post-intervention ] [ Designated as safety issue: No ]
- Physical and mental health status [ Time Frame: Measured at pre- and post-intervention ] [ Designated as safety issue: No ]
- Medical service use patterns [ Time Frame: Measured at pre- and post-intervention ] [ Designated as safety issue: No ]
- Medication use [ Time Frame: Measured throughout the study ] [ Designated as safety issue: No ]
- Neurocognition [ Time Frame: Measured at baseline ] [ Designated as safety issue: No ]
- Substance abuse [ Time Frame: Measured at pre- and post-intervention ] [ Designated as safety issue: No ]
- Psychiatric symptoms [ Time Frame: Measured at pre- and post-intervention ] [ Designated as safety issue: No ]
- Amount and seriousness of related comorbidities [ Time Frame: Measured at pre- and post-intervention ] [ Designated as safety issue: No ]
- Quantitative and qualitative survey ratings [ Time Frame: Measured throughout the study ] [ Designated as safety issue: No ]
| Estimated Enrollment: | 100 |
| Study Start Date: | September 2007 |
| Estimated Study Completion Date: | March 2010 |
| Estimated Primary Completion Date: | March 2010 (Final data collection date for primary outcome measure) |
| Arms | Assigned Interventions |
|---|---|
|
Experimental: 1
Participants will receive a self-management program for chronic illness
|
Behavioral: Self-management program for chronic illness
Self-management program for chronic illness will include between 10 and 16 psychoeducational and supportive group sessions.
|
Detailed Description:
Schizophrenia is a life-long brain disorder affecting approximately 1 percent of Americans each year. Schizophrenia can be extremely disabling, causing people to hear voices, experience paranoia or hallucinations, and believe that others are controlling their thoughts. People with schizophrenia also experience increased rates of concurrent medical conditions, such as diabetes, respiratory illness, and heart disease. This can make holding a job or even caring for oneself very difficult. The purpose of this study is to develop and evaluate a self-management program for adults living with both schizophrenia and a concurrent medical condition.
Participants in this open-label study will attend 10 to 16 group sessions led by two group leaders. Group sessions will meet each week for an hour during which participants will learn new skills to help them take responsibility for the daily management of chronic medical conditions. In addition to learning how to communicate more effectively with medical providers, participants will learn about healthy eating, the importance of physical activity, addictive behaviors that can worsen health conditions, and proper use of medications. Homework will be assigned weekly for participants to review skills learned in each session. After each session, participants will complete a survey to evaluate the session's effectiveness. At the end of the study, participants will attend one additional group meeting and an individual interview to discuss the overall effectiveness of the intervention and their experiences in the group sessions. The results of this study will be used to evaluate and improve the self-management program for future use.
Eligibility| Ages Eligible for Study: | 18 Years to 64 Years |
| Genders Eligible for Study: | Both |
| Accepts Healthy Volunteers: | No |
Inclusion Criteria:
- Meets DSM-IV criteria for schizophrenia or schizoaffective disorder
- Current documented chart diagnosis of at least one chronic medical condition
- Received clinic services for a minimum of 3 months prior to study entry
- English-speaking
- Willing to use an effective form of birth control throughout the study if sexually active
Exclusion Criteria:
- History of a serious neurological disorder or head trauma with loss of consciousness
- Diagnosed with mental retardation or dementia
- Diagnosed with end stage organ disease
- Currently receiving chemotherapy and/or radiation treatment for cancer
- Received psychiatric hospitalization less than 3 months prior to study entry date
- Blind and/or deaf
- Pregnant
- Infected with HIV with a CD4 count under 350
- Diagnosis of AIDS
- Diagnosis of anorexia
- Problematic substance use, as defined by a mental health provider
- Psychiatric instability, as defined by a mental health provider
Contacts and Locations| Contact: Richard W. Goldberg, PhD | 410-706-8473 | rgoldber@psych.umaryland.edu |
| Contact: Wendy L. Potts, MS | 410-706-6638 | wpotts@psych.umaryland.edu |
| United States, Maryland | |
| Fayette Street Clinics | Recruiting |
| Baltimore, Maryland, United States, 21201 | |
| Contact: Richard W. Goldberg, PhD 410-706-8473 rgoldber@psych.umaryland.edu | |
| Contact: Wendy Potts 410-706-2490 wpotts@psych.umaryland.edu | |
| Principal Investigator: Richard W. Goldberg, PhD | |
| Principal Investigator: | Richard W. Goldberg, PhD | University of Maryland |
More Information
No publications provided
| Responsible Party: | William T. Riely, Program Official, NIMH |
| ClinicalTrials.gov Identifier: | NCT00525304 History of Changes |
| Other Study ID Numbers: | R34 MH078168, DAHBR 96-BHB |
| Study First Received: | September 4, 2007 |
| Last Updated: | March 30, 2009 |
| Health Authority: | United States: Federal Government |
Keywords provided by National Institute of Mental Health (NIMH):
|
medical co-morbidity diabetes heart disease respiratory illness |
Additional relevant MeSH terms:
|
Schizophrenia Schizophrenia and Disorders with Psychotic Features Mental Disorders |
ClinicalTrials.gov processed this record on May 19, 2013