Peer Support for Increasing Physical Activity in People With Serious Mental Illnesses
Status
Conditions
Treatments
Study type
Funder types
Identifiers
Details and patient eligibility
About
This study will determine the effectiveness of a peer support system in increasing physical activity and effecting health behavior change in people with serious mental illnesses.
Full description
People with serious mental illnesses (SMIs) are, by definition, significantly functionally impaired by the illness for an indefinite period of time. Schizophrenia, major depression, and bipolar disorder are considered SMIs. Severe anxiety disorders, cognitive disorders, and some personality disorders are sometimes categorized as SMIs, as well. The rate of obesity among people with SMIs is higher than that of people without mental illnesses. This disparity may be due to the negative symptoms that people with SMIs experience, such as vulnerability to stress, extreme dependency, and lack of motivation. This study will design and test a culturally appropriate physical activity intervention based on a peer support model for people with SMIs in an urban community psychiatry program. The intervention will be evaluated to determine its effectiveness in increasing physical activity and effecting health behavior change in people with SMIs.
Participants in this 4-month, open-label study will be randomly assigned to participate in either a physical activity intervention with peer support (PA+PS) or a physical activity intervention without peer support (PA). Participants in the PA+PS group will have three exercise sessions each week, which will include group exercise classes and open gym hours for supervised individual exercise. They will also meet with a peer educator once a week for 15 minutes. Peer educators will provide emotional, informational, instrumental, and appraisal support that is aimed to motivate participants to partake in the exercise sessions. Participants in the PA group will attend the three weekly exercise sessions but will not attend meetings with the peer educator. All outcomes will be assessed at a follow-up visit at the end of the intervention.
Enrollment
Sex
Ages
Volunteers
Inclusion criteria
- Patient at the Johns Hopkins Community Psychiatry program
- Plans to remain in Baltimore for 8 months after study entry
- If currently breastfeeding, has received approval from a physician to participate in the study
Exclusion criteria
- Any condition that would make weight loss medically inadvisable
- Diagnosis of or treatment for cancer (except non-melanoma skin cancer) within 2 years prior to study entry
- Liver failure
- History of anorexia nervosa
- Pregnant or planning to become pregnant during the study
- Inability to walk or participate in an exercise class
- Consumes more than 14 alcoholic drinks per week
- Symptoms of angina or a cardiovascular event within 6 months prior to study entry
Trial design
Primary purpose
Allocation
Interventional model
Masking
100 participants in 2 patient groups
Trial contacts and locations
Loading...
Data sourced from clinicaltrials.gov
Clinical trials
Research sites
Resources
Legal