Prohealth
Baltimore, Maryland, 21207, United States
NCT Number: NCT00902694
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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Notify Me18 year and older
All sexes
Interventional
Not applicable
Baltimore, Maryland, 21207, United States
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.
Healthy volunteers accepted: No
Only the study team can determine whether someone qualifies for participation.
Age 18 and older;
Exclusion criteria
Use of prescription weight loss medication or over-the-counter orlistat within 3 months
if participant does not agree to stop taking it;
Group and individual weight loss counseling and group physical activity classes for 18 months
group health classes quarterly with topics not related to weight
Time frame: 6 and 18 months
Change is from baseline to 6 months and baseline to 18 months
Time frame: Baseline, 6 and 18 months
Minutes cycled during standardized cycle ergometry testing protocol; higher number of minutes cycled indicates better outcome.
Time frame: Measured at baseline, 6 and 18 months
Change in waist circumference in centimeters (cm) from baseline to 18 months
Time frame: Measured at baseline, 6 and 18 months
Change in systolic and diastolic blood pressure (mmHg) from baseline to 18 months
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
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
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.
Time frame: Baseline, 6 and 18 months
Total score range between 0 and 60, higher scores indicating more depressive symptoms
Johns Hopkins University
Other
Randomized Trial Of Achieving Healthy Lifestyles In Psychiatric Rehabilitation
Acronym: ACHIEVE
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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