Clinical Trials Logo

Clinical Trial Details — Status: Completed

Administrative data

NCT number NCT01854320
Other study ID # R01DK095069
Secondary ID
Status Completed
Phase N/A
First received
Last updated
Start date July 2012
Est. completion date June 2018

Study information

Verified date August 2018
Source Drexel University
Contact n/a
Is FDA regulated No
Health authority
Study type Interventional

Clinical Trial Summary

The primary goal of this project is to determine if an innovative behavioral weight loss program that incorporates new developments from the field of behavior therapy produces superior weight control than standard behavioral treatment. A sample of 200 adults from the community are participating in this study.


Recruitment information / eligibility

Status Completed
Enrollment 192
Est. completion date June 2018
Est. primary completion date June 2018
Accepts healthy volunteers Accepts Healthy Volunteers
Gender All
Age group 18 Years to 70 Years
Eligibility Inclusion Criteria:

- Be between the ages of 18 and 70

- Have a BMI between 27-50

- Have the ability to engage in physical activity (i.e., can walk at least 2 blocks without stopping for rest).

- Agree to provide permission for the research team to regularly contact your physician throughout the study to share information on changes in your weight.

- Successfully complete all steps in the enrollment process

Exclusion Criteria:

- You have a medical condition or psychiatric condition that may limit your ability to comply with the behavioral recommendations of the program or pose a risk to you during weight loss.

- You are pregnant or plan to become pregnant in the next three years.

- Report recently beginning a course of or changing the dosage of prescription medications that can cause significant weight loss or weight gain.

- You are participating in or plan to participate in another weight loss program in the next three years.

- The research team identifies any factors that would render you potentially unable or unlikely to follow the protocol, or unable to benefit from it.

Study Design


Intervention

Behavioral:
Acceptance-based treatment

Standard behavioral treatment


Locations

Country Name City State
United States Drexel University Philadelphia Pennsylvania

Sponsors (1)

Lead Sponsor Collaborator
Drexel University

Country where clinical trial is conducted

United States, 

Outcome

Type Measure Description Time frame Safety issue
Primary Weight Baseline - 2-year follow-up