Evaluation of the In SHAPE Fitness Intervention for Adults With Serious Mental Illness

January 7, 2015 updated by: Dartmouth-Hitchcock Medical Center

Promoting Health and Functioning in Persons With SMI

Few studies targeting obesity in serious mental illness have reported clinically significant risk reduction, and non have been replicated in community settings or demonstrated sustained outcomes after intervention withdrawal. The researchers sought to replicate positive health outcomes demonstrated in a previous randomized effectiveness study of the In SHAPE program across urban community mental health organizations serving an ethnically diverse population.

Study Overview

Detailed Description

In this randomized, controlled study, 133 adults age 21 and older with serious mental illness (SMI) and poor physical fitness (BMI>25, or <10 minutes of exercise 2x over the past month) were randomized to either: a) In SHAPE Lifestyles (ISL) intervention or b) Health Club Membership and Education (HCME): consisting of a YMCA membership, educational materials on exercise and healthy diet, and an on-site introduction to the health club. The following three specific aims were addressed: 1) To compare ISL and HCME with respect to: a) participation in regular exercise and dietary change; (b) participation in preventive health care; and (c) improved fitness and health; (2) to compare ISL and HCME with respect to: (a) indicators of mental health and (b) personal self-efficacy; and (3) to explore differences in ISL and HCME with respect to (a) selected physical, metabolic, dietary, and community functioning secondary outcomes; and (b) the relationship of demographic variables and readiness to change to outcomes. ISL participants received a 6-month intensive program of one-to-one health mentoring, followed by a 3-month period of transitioning to self-directed individual and group programming, with assessments conducted at baseline, 3, 6, 9, and 12 months. If found to be effective, ISL will provide a practical approach to improving health, independent functioning, and longevity in disabled persons with SMI.

Study Type

Interventional

Enrollment (Actual)

133

Phase

  • Not Applicable

Contacts and Locations

This section provides the contact details for those conducting the study, and information on where this study is being conducted.

Study Locations

    • New Hampshire
      • Concord, New Hampshire, United States, 03301
        • Riverbend Community Mental Health

Participation Criteria

Researchers look for people who fit a certain description, called eligibility criteria. Some examples of these criteria are a person's general health condition or prior treatments.

Eligibility Criteria

Ages Eligible for Study

17 years and older (Adult, Older Adult)

Accepts Healthy Volunteers

No

Genders Eligible for Study

All

Description

Inclusion Criteria:

  • Age 21 or older
  • Serious mental illness defined by an axis I diagnosis of major depression, bipolar disorder, schizoaffective disorder, or schizophrenia
  • Persistent impairment in multiple areas of functioning (e.g., work, school, self-care)
  • Body mass index (BMI) greater than 25
  • Able and willing to provide informed consent
  • On stable pharmacological treatment (same psychiatric medications over prior 2 months)

Exclusion Criteria:

  • Residing in a nursing home of other institution
  • Diagnosis of dementia or significant cognitive impairment (MMSE<24)
  • Unable to walk one city block
  • Pregnant or planning to become pregnant within the next 18 months
  • Unable to speak English
  • Terminal illness with life expectancy <1 year
  • Current diagnosis of an active substance dependence disorder

Study Plan

This section provides details of the study plan, including how the study is designed and what the study is measuring.

How is the study designed?

Design Details

  • Primary Purpose: Prevention
  • Allocation: Randomized
  • Interventional Model: Parallel Assignment
  • Masking: Single

Arms and Interventions

Participant Group / Arm
Intervention / Treatment
Experimental: In SHAPE Lifestyles
In SHAPE Lifestyle is a health promotion intervention consisting of a fitness club membership and a health promotion coach with basic certification as a fitness trainer, instruction on principles of healthy eating and nutrition, and training in tailoring individual wellness plans to the needs of persons with serious mental illness.
In SHAPE Lifestyles is a health promotion intervention consisting of a fitness club membership and a health promotion coach with basic certification as a fitness trainer, instruction on principles of healthy eating and nutrition, and training in tailoring individual wellness plans to the needs of persons with serious mental illness.
Active Comparator: Health Club Membership and Education
Fitness club membership with education in using the exercise equipment.
Fitness club membership with education in using the exercise equipment.

What is the study measuring?

Primary Outcome Measures

Outcome Measure
Measure Description
Time Frame
Change in Exercise Capacity
Time Frame: Baseline, 3-, 6-, 9-, and 12-months
Change in fitness as measured by the 6-minute walk test.
Baseline, 3-, 6-, 9-, and 12-months

Secondary Outcome Measures

Outcome Measure
Measure Description
Time Frame
Body Mass Index
Time Frame: Baseline, 3-, 6-, 9-, and 12-months
Baseline, 3-, 6-, 9-, and 12-months
Change in Weight
Time Frame: Baseline, 3-, 6-, 9-, and 12-months
Change in weight over time was measured at baseline, 3-, 6-, 9-, and 12-months. Measures were weight (lbs).
Baseline, 3-, 6-, 9-, and 12-months
Change in Triglycerides and Cholesterol
Time Frame: Baseline, 3-, 6-, 9-, and 12-months
Change in triglycerides and cholesterol measured with the CardioChek PA Analyzer: Fasting blood glucose and lipids.
Baseline, 3-, 6-, 9-, and 12-months
Change in Health Status
Time Frame: Baseline, 3-, 6-, 9-, and 12-months
Change in health status was measured by the SF-12: Medical Outcomes Study Short Form -12
Baseline, 3-, 6-, 9-, and 12-months
Change in Community Functioning
Time Frame: Baseline, 9-, and 12-months
Change in community functioning was measured by the ILSS: Independent Living Skills Scale
Baseline, 9-, and 12-months
Change in Physical Measurements (Fitness)
Time Frame: Baseline, 3-, 6-, 9-, and 12-months
Change is physical measurements was determined by measuring waist circumference and resting pulse
Baseline, 3-, 6-, 9-, and 12-months
Change in Psychological State
Time Frame: Baseline, 3-, 6-, 9-, and 12-months
Change in psychological state was measured using the CESD: Cntr Epid Studies Dep; SANS: Scale Assess Neg Sx; R-SES: Revised Self-efficacy Scale
Baseline, 3-, 6-, 9-, and 12-months
Change in Participation in Exercise
Time Frame: Baseline, 3-, 6-, 9-, and 12-months
Change in participation in exercise was determined by measuring weekly exercise at 3-, 6-, 9-, and 12-months using a physical activity log; weekly health club attendance at 3-, 6-, 9-, and 12-months based on frequency of YMCA visits; total physical activity at baseline, 3-, 6-, 9-, and 12-months based on the YPAS: Yale Physical Activity Scale.
Baseline, 3-, 6-, 9-, and 12-months
Change in Diet Behaviors
Time Frame: Baseline, 3-, 6-, 9-, and 12-months
Change in diet behaviors was measured based on the WLB-SOC: Weight Loss Behavior State of Change Scale.
Baseline, 3-, 6-, 9-, and 12-months
Change in Preventative Health Care
Time Frame: Baseline and 12-months
Change in preventative health care was based on the PHC: Preventative Healthcare Checklist
Baseline and 12-months

Collaborators and Investigators

This is where you will find people and organizations involved with this study.

Investigators

  • Principal Investigator: Stephen J Bartels, MD,MS, Dartmouth-Hitchcock Medical Center

Study record dates

These dates track the progress of study record and summary results submissions to ClinicalTrials.gov. Study records and reported results are reviewed by the National Library of Medicine (NLM) to make sure they meet specific quality control standards before being posted on the public website.

Study Major Dates

Study Start

September 1, 2006

Primary Completion (Actual)

August 1, 2009

Study Completion (Actual)

August 1, 2009

Study Registration Dates

First Submitted

January 6, 2015

First Submitted That Met QC Criteria

January 7, 2015

First Posted (Estimate)

January 8, 2015

Study Record Updates

Last Update Posted (Estimate)

January 8, 2015

Last Update Submitted That Met QC Criteria

January 7, 2015

Last Verified

January 1, 2015

More Information

This information was retrieved directly from the website clinicaltrials.gov without any changes. If you have any requests to change, remove or update your study details, please contact register@clinicaltrials.gov. As soon as a change is implemented on clinicaltrials.gov, this will be updated automatically on our website as well.

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