- ICH GCP
- US Clinical Trials Registry
- Clinical Trial NCT01937845
Evaluating the Health Outcomes of the Joslin Why WAIT? Program
March 6, 2024 updated by: Joslin Diabetes Center
Evaluating the Health Outcomes of the Joslin Why WAIT? Program (Weight Achievement & Intensive Treatment Program)
Evaluating the health outcomes of patients that were enrolled in Joslin's Why WAIT Program.
These outcomes include BMI, A1C, lipid profile.
Study Overview
Detailed Description
This study is aimed to evaluate the health outcomes of patients enrolled in Joslin's Why WAIT Program.
This program aims to control diabetes and help patients lose weight.
Study Type
Observational
Enrollment (Actual)
110
Participation Criteria
Researchers look for people who fit a certain description, called eligibility criteria. Some examples of these criteria are a person's general health condition or prior treatments.
Eligibility Criteria
Ages Eligible for Study
18 years to 90 years (Adult, Older Adult)
Accepts Healthy Volunteers
No
Sampling Method
Non-Probability Sample
Study Population
Patients with Type 2 diabetes enrolled in the Why WAIT?
Program
Description
Inclusion Criteria:
- Patients with Type 2 diabetes with BMI over 35
Exclusion Criteria:
- Patients with type 1 diabetes
Study Plan
This section provides details of the study plan, including how the study is designed and what the study is measuring.
How is the study designed?
Design Details
What is the study measuring?
Primary Outcome Measures
Outcome Measure |
Time Frame |
---|---|
Weight loss of 7% body weight
Time Frame: 13 weeks
|
13 weeks
|
Collaborators and Investigators
This is where you will find people and organizations involved with this study.
Sponsor
Publications and helpful links
The person responsible for entering information about the study voluntarily provides these publications. These may be about anything related to the study.
Study record dates
These dates track the progress of study record and summary results submissions to ClinicalTrials.gov. Study records and reported results are reviewed by the National Library of Medicine (NLM) to make sure they meet specific quality control standards before being posted on the public website.
Study Major Dates
Study Start
August 1, 2006
Primary Completion (Estimated)
September 1, 2025
Study Completion (Estimated)
December 1, 2025
Study Registration Dates
First Submitted
September 4, 2013
First Submitted That Met QC Criteria
September 9, 2013
First Posted (Estimated)
September 10, 2013
Study Record Updates
Last Update Posted (Actual)
March 8, 2024
Last Update Submitted That Met QC Criteria
March 6, 2024
Last Verified
March 1, 2024
More Information
Terms related to this study
Other Study ID Numbers
- CHS#: 06-26
Plan for Individual participant data (IPD)
Plan to Share Individual Participant Data (IPD)?
NO
Drug and device information, study documents
Studies a U.S. FDA-regulated drug product
No
Studies a U.S. FDA-regulated device product
No
This information was retrieved directly from the website clinicaltrials.gov without any changes. If you have any requests to change, remove or update your study details, please contact register@clinicaltrials.gov. As soon as a change is implemented on clinicaltrials.gov, this will be updated automatically on our website as well.
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