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Clinical Trial Details — Status: Completed

Administrative data

NCT number NCT00606840
Other study ID # #2018-07
Secondary ID
Status Completed
Phase N/A
First received January 22, 2008
Last updated April 12, 2012
Start date January 2008
Est. completion date September 2008

Study information

Verified date April 2012
Source The Miriam Hospital
Contact n/a
Is FDA regulated No
Health authority United States: Institutional Review Board
Study type Interventional

Clinical Trial Summary

The specific aim of the proposed project is to test two separate self-regulation interventions to prevent weight gain in young adults, one based on making sustained small changes in behavior to prevent weight gain and the other on making periodic larger behavior changes resulting in weight loss.


Recruitment information / eligibility

Status Completed
Enrollment 52
Est. completion date September 2008
Est. primary completion date September 2008
Accepts healthy volunteers No
Gender Both
Age group 18 Years to 35 Years
Eligibility Inclusion Criteria:

- Age 18-35

- Body mass index between 23 and 30

- Interested in preventing weight gain

Exclusion Criteria:

- BMI outside of range specified

- Age outside of range specified

- History of or current eating disorder or substance abuse

- Recent weight loss greater than 5% of weight

- Currently in another research study that would interfere

Study Design

Allocation: Randomized, Intervention Model: Parallel Assignment, Masking: Single Blind (Outcomes Assessor), Primary Purpose: Prevention


Related Conditions & MeSH terms


Intervention

Behavioral:
large changes in eating and activity
Behavioral self-regulation interventions to prevent weight gain in young adults.
small changes in eating and activity
Behavioral self-regulation interventions to prevent weight gain in young adults.

Locations

Country Name City State
United States The Miriam Hospital Providence Rhode Island

Sponsors (1)

Lead Sponsor Collaborator
The Miriam Hospital

Country where clinical trial is conducted

United States, 

Outcome

Type Measure Description Time frame Safety issue
Primary weight change 8 weeks and 16 weeks No
Secondary frequency of weighing, adherence to intervention, diet, activity 8 weeks and 16 weeks No
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