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Clinical Trial Details — Status: Completed

Administrative data

NCT number NCT03680703
Other study ID # 2000023155
Secondary ID
Status Completed
Phase N/A
First received
Last updated
Start date July 20, 2018
Est. completion date December 31, 2019

Study information

Verified date January 2020
Source Yale University
Contact n/a
Is FDA regulated No
Health authority
Study type Interventional

Clinical Trial Summary

The purpose of the study is to conduct a randomized clinical trial examining the feasibility and effectiveness of two guided self-help behavioral weight loss (gshBWL) treatments delivered via the internet for individuals struggling with weight loss one year following bariatric surgery. The two treatments will consist of 1) gshBWL delivered through the internet only (gshBWL-I) and 2) gshBWL delivered via the internet with additional complementary phone sessions (gshBWL-IP).


Recruitment information / eligibility

Status Completed
Enrollment 33
Est. completion date December 31, 2019
Est. primary completion date December 31, 2019
Accepts healthy volunteers No
Gender All
Age group 18 Years to 70 Years
Eligibility Inclusion Criteria:

- gastric bypass and sleeve surgery patients from Yale's Bariatric/Gastrointestinal Surgery Program

- surgery 1-2 years prior

- <60% excess weight loss

- able to read English proficiently enough to read the patient self-help materials and study assessments

- available for the duration of the treatment

- availability of internet and phone to participate in study interventions

- agree to the study procedures

Exclusion Criteria:

- medical status judged by the surgeon as contraindication (rare instances of need for additional surgery or medical instability)

- unable to ambulate

- current medications that influence eating/weight

- current substance dependence or other severe psychiatric disturbance (e.g., suicidality) that requires immediate treatment.

Study Design


Related Conditions & MeSH terms


Intervention

Behavioral:
Guided Self-Help Behavioral Weight Loss
Participants will be provided with patient-focused materials and worksheets that contain all the necessary information, procedures, and techniques of the behavioral weight loss program. For 12 weeks, treatment will be provided over the internet. This therapy focuses on making gradual and modest lifestyle changes with goals of normalizing eating patterns, decreasing caloric intake, building coping skills, and increasing physical activity.

Locations

Country Name City State
United States Yale Department of Psychiatry New Haven Connecticut

Sponsors (1)

Lead Sponsor Collaborator
Yale University

Country where clinical trial is conducted

United States, 

Outcome

Type Measure Description Time frame Safety issue
Primary Weight Change Percent weight loss (in pounds) from baseline. 3 months
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