- ICH GCP
- US Clinical Trials Registry
- Clinical Trial NCT05601804
TARGETing Healthy Weight Loss in the Context of Food Insecurity (TARGET P&F I)
October 10, 2023 updated by: Candice A. Myers, Ph.D., Pennington Biomedical Research Center
TARGETing Healthy Weight Loss in the Context of Food Insecurity Pilot and Feasibility Trial I
This pilot and feasibility study will collect information from food insecure, as well as food secure, women with obesity to detail their desires and needs for healthy weight reduction.
Up to 60 women with obesity will be enrolled.
Pennington Biomedical Research Center will coordinate this qualitative study and use focus groups discussion to collect formative data.
Study Overview
Status
Active, not recruiting
Conditions
Study Type
Observational
Enrollment (Actual)
45
Contacts and Locations
This section provides the contact details for those conducting the study, and information on where this study is being conducted.
Study Contact
- Name: Candice A. Myers, PhD
- Phone Number: 225-763-2849
- Email: candice.myers@pbrc.edu
Study Locations
-
-
Louisiana
-
Baton Rouge, Louisiana, United States, 70808
- Pennington Biomedical Research Center
-
-
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 65 years (Adult, Older Adult)
Accepts Healthy Volunteers
Yes
Sampling Method
Non-Probability Sample
Study Population
Women aged 18 to 65 years with a BMI of 30.0 kg/m2 or greater.
Description
Inclusion Criteria:
- Willing to provide written informed consent
- Female
- 18 to 65 years of age
- BMI ≥ 30 kg/m2
- Ability to read and write using English
- Willing to participate in focus group discussions
- Willing to be audio/video recorded
Exclusion Criteria:
- Male
- Currently pregnant
- BMI <30 kg/m2
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
- Observational Models: Other
- Time Perspectives: Cross-Sectional
Cohorts and Interventions
Group / Cohort |
---|
Food Insecure Women with Obesity
4 focus groups with 6-8 participants each
|
Food Secure Women with Obesity
3 focus groups with 6-8 participants each
|
What is the study measuring?
Primary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
---|---|---|
Desires and needs for weight loss
Time Frame: Through study completion, up to 1 year
|
Via focus group discussions, we will elicit in-depth information from women with food insecurity and obesity to detail their desires and needs for weight loss.
|
Through study completion, up to 1 year
|
Collaborators and Investigators
This is where you will find people and organizations involved with this study.
Investigators
- Principal Investigator: Candice A. Myers, PhD, Pennington Biomedical Research Center
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 (Actual)
September 1, 2022
Primary Completion (Estimated)
August 31, 2024
Study Completion (Estimated)
August 31, 2024
Study Registration Dates
First Submitted
October 21, 2022
First Submitted That Met QC Criteria
October 26, 2022
First Posted (Actual)
November 1, 2022
Study Record Updates
Last Update Posted (Actual)
October 11, 2023
Last Update Submitted That Met QC Criteria
October 10, 2023
Last Verified
October 1, 2023
More Information
Terms related to this study
Keywords
Additional Relevant MeSH Terms
Other Study ID Numbers
- PBRC 2022-039
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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