Motivational Interviewing for Weight Loss With Young Adults

Completed · Not applicable

Conditions studied: Obesity

In brief

This study is a 2-arm randomized controlled trial to evaluate the feasibility, acceptability and preliminary efficacy of an MI-based program for weight loss in young adults.

Key facts

Study ID

NCT01899625

Run by

Virginia Commonwealth University

People needed

51

Starts

2012-09-01

Expected to finish

2014-10-01

Last updated by the study team

2016-02-26

Who can join

Age: 18 and older, up to 25. Sex: any. Healthy volunteers: not accepted.

You may qualify if…

• Between 18-25 years of age.
• Body Mass Index (BMI) between 25 and 45 kg/m2.
• Men and women will be recruited.
• All race and ethnic groups will be recruited.

You may not qualify if…

• Currently receiving treatment for Type 2 Diabetes, hypertension, hyperlipidemia, or report a history of cardiovascular disease.
• Other health problems which may influence the ability to walk for physical activity or be associated with unintentional weight change, including cancer treatment within the past 5 years or tuberculosis.
• Report a history of, or current diagnosed DSM-IV-TR eating disorder (i.e., anorexia nervosa or bulimia nervosa) or any current compensatory behaviors (e.g., vomiting, laxative use, excessive exercise).
• Report a heart condition, chest pain during periods of activity or rest, or loss of consciousness on the Physical Activity Readiness Questionnaire (PAR-Q). Individuals endorsing joint problems, prescription medication usage, or other medical conditions that could limit exercise will be required to obtain written physician consent to participate.
• Report a history of any psychotic disorder, bipolar disorder, or organic brain syndromes; report hospitalization for any psychiatric disorder within the last 12 months.
• Are currently participating in a weight loss program and/or taking weight loss medication.
• Lost > 5% of body weight during the past 6 months or history of bariatric surgery.
• Participation in any other research study that may interfere with this study.
• Intend to move outside of the surrounding area within the time frame of the investigation or will be out of town / unavailable for three or more weeks during the initial intervention period.
• Are pregnant, lactating, less than 6 months post-partum, or plan to become pregnant during the time frame of the investigation.
• Failure to complete screening appointments. -

Where it is running

• Virginia Commonwealth University School of Medicine — Richmond, Virginia, United States

Full record on ClinicalTrials.gov

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