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Peer Support for Increasing Physical Activity in People With Serious Mental Illnesses

Activating Consumers to Exercise in Community Psychiatry Through Peer Support

Status
Completed
Phases
NA
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT00458094
Enrollment
100
Registered
2007-04-09
Start date
2007-03-31
Completion date
2009-12-31
Last updated
2017-12-06

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

Conditions

Anxiety Disorders, Bipolar Disorder, Cognitive Disorders, Depression, Personality Disorders, Schizophrenia

Keywords

Exercise, Mental Illness, Community Psychiatry, Peer Support, Mental Disorders

Brief summary

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.

Detailed 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.

Interventions

BEHAVIORALPhysical activity intervention with peer support (PA+PS)

Participants in the PA+PS group will have three exercise sessions each week for 4 months, 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.

BEHAVIORALPhysical activity intervention without peer support (PA)

Participants in the PA group will attend the three weekly exercise sessions for 4 months but will not attend meetings with the peer educator.

Sponsors

National Institute of Mental Health (NIMH)
CollaboratorNIH
Johns Hopkins University
Lead SponsorOTHER

Study design

Allocation
RANDOMIZED
Intervention model
PARALLEL
Primary purpose
TREATMENT
Masking
SINGLE (Outcomes Assessor)

Eligibility

Sex/Gender
ALL
Age
18 Years to 70 Years
Healthy volunteers
Yes

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

Design outcomes

Primary

MeasureTime frame
Cardiorespiratory fitnessMeasured at Month 4

Secondary

MeasureTime frame
Waist circumferenceMeasured at Month 4
Physical activityMeasured at Month 4
Health statusMeasured at Month 4
WeightMeasured at Month 4
Exercise-related self-efficacyMeasured at Month 4
General perceived efficacyMeasured at Month 4
ParticipationMeasured at Month 4
Center for Epidemiology Depression ScaleMeasured at Month 4

Countries

United States

Outcome results

None listed

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