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Completed

NCT Number: NCT00902694

Randomized Trial Of Achieving Healthy Lifestyles In Psych Rehabilitation

This study will determine whether a behavioral weight loss intervention including dietary counseling and exercise is effective in helping people with serious mental illnesses lose weight.

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Key information

Age range

18 year and older

Sex eligibility

All sexes

Study type

Interventional

Phase

Not applicable

Primary location

Prohealth

Baltimore, Maryland, 21207, United States

About this study

The objective of this study is to perform a randomized clinical trial (ACHIEVE) to definitively test the efficacy of an innovative, practical intervention to accomplish weight loss in overweight and obese persons with SMI. This multi-site trial will enroll consumers with SMI who attend ten psychiatric rehabilitation centers in Maryland and randomize participants to the ACHIEVE intervention or control. Intervention participants will receive group and individual weight loss counseling sessions and group physical activity classes. Co-primary outcomes will be change in weight from baseline to 6 and 18 months.

Who can participate

Healthy volunteers accepted: No

Only the study team can determine whether someone qualifies for participation.

Age 18 and older;

  • Overweight, defined by Body Mass Index at least 25.0 kg/m2;
  • Able and willing to give informed consent and participate in the intervention;
  • On the same psychiatric medications within the 30 days before baseline weight (dose changes allowed;)
  • Able to attend at least 2 intervention sessions per week during initial 6-month phase;

Exclusion criteria

  • Contraindication to weight loss
  • Receiving active cancer treatment (radiation/chemotherapy)
  • Liver failure
  • History of anorexia nervosa;
  • Cardiovascular event (unstable angina, myocardial infarction) within previous 6 months;
  • Prior or planned bariatric surgery;

Use of prescription weight loss medication or over-the-counter orlistat within 3 months

if participant does not agree to stop taking it;

  • Twenty pound or greater weight loss in 3 months prior to baseline, as documented by staff measurement;
  • Inability to walk to participate in exercise class;
  • Pregnant or planning a pregnancy during study period. Nursing mothers would need approval from physician;
  • Alcohol or substance use disorder either: 1) active and determined to be incompatible with participation in the intervention through discussion with program staff; or 2) new abstinence from alcohol or substance use disorder in past 30 days;
  • Planning to leave rehabilitation center within 6 months or move out of geographic area within 18 months;
  • Investigator judgment (e.g., for concerns over safety, adherence or follow-up);
  • Weight greater than 400 pounds.

Treatment and study plan

ACHIEVE Intervention

Behavioral

Group and individual weight loss counseling and group physical activity classes for 18 months

Control

Other

group health classes quarterly with topics not related to weight

Primary outcomes

  1. Change in Weight Loss in Kilograms (kg)

    Time frame: 6 and 18 months

    Change is from baseline to 6 months and baseline to 18 months

Secondary outcomes

  1. Minutes Cycled During Cycle Ergometry Testing

    Time frame: Baseline, 6 and 18 months

    Minutes cycled during standardized cycle ergometry testing protocol; higher number of minutes cycled indicates better outcome.

  2. Change in Waist Circumference in Centimeters (cm)

    Time frame: Measured at baseline, 6 and 18 months

    Change in waist circumference in centimeters (cm) from baseline to 18 months

  3. Change in Systolic and Diastolic Blood Pressure (mmHg)

    Time frame: Measured at baseline, 6 and 18 months

    Change in systolic and diastolic blood pressure (mmHg) from baseline to 18 months

  4. Change in Lipids (Total Cholesterol, LDL, HDL and Triglyceride (mg/dL)

    Time frame: Measured at baseline, 6 and 18 months

    Change in Lipids (total cholesterol, LDL, HDL and Triglyceride (mg/dL) from baseline to 18 months

  5. Framingham Cardiovascular Risk Score

    Time frame: Measured at baseline, 6 and 18 months

    Higher score indicates greater cardiovascular risk. The score can range from 0-38 with higher scores yielding increased 10-year probability of stroke

  6. Health Status as Measured by the SF-12

    Time frame: Baseline, 6 and 18 months

    Health status reported for the SF-12 in two subscales-physical component summary (PCS) and the mental component summary (MCS). Subscale score ranges from 0-100 with higher scores indicating better physical or mental health.

  7. Depression Assessed by Center for Epidemiologic Studies Depression Scale (CES-D)

    Time frame: Baseline, 6 and 18 months

    Total score range between 0 and 60, higher scores indicating more depressive symptoms

Sponsors and collaborators

Lead sponsor

Johns Hopkins University

Other

Collaborators

  • National Institute of Mental Health (NIMH)

Registry information

Official study title

Randomized Trial Of Achieving Healthy Lifestyles In Psychiatric Rehabilitation

Acronym: ACHIEVE

Important dates

Study start
2008
Primary completion
2012
Study completion
2012
First posted
May 15, 2009
Registry last updated
Jul 30, 2025

OpenTrials presents study information sourced from ClinicalTrials.gov. The official registry record should be consulted for the latest information.

View the official ClinicalTrials.gov record (opens in a new tab)

This listing is for discovery and informational purposes only. It is not medical advice, does not guarantee that a study is recruiting, and does not determine eligibility. Contact the study team and a qualified healthcare professional when considering participation.

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