Self-monitoring Focus Groups With Vibrant Lives Pasadena Participants
For patients and families
In plain language
An automatic summary of structured registry data. It is an orientation aid, not a substitute for the official protocol or a physician assessment.
- What is being studied
- The protocol lists: Discussion, Interview, Survey Administration.
- Who it may be relevant to
- Registry conditions: Obesity-Related Malignant Neoplasm. Basic parameters: No limits · All.
- What needs checking
- Age, condition and sex are only basic indicators. Prior treatment, laboratory values and other mandatory requirements appear in the eligibility criteria below.
- Where it takes place
- United States
- Next step
- Save the trial, show it to the treating physician, and confirm current recruitment with the study center. Costs, documents and travel →
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Official title
Self-Monitoring Focus Groups With Vibrant Lives Pasadena Participants
Overview
This study investigates how individuals feel about a dietary mobile application. Information collected from focus groups and interviews may help doctors and mobile application developers to determine preferences and participant feedback about the appeal and usefulness of a mobile application.
Detailed description
PRIMARY OBJECTIVE:
I. To gather qualitative data to assess appeal, preference, and usefulness of a food and beverage self-monitoring mobile application.
OUTLINE:
PHASE I: Participants attend 4 sessions of focus groups.
PHASE II: Participants attend virtual Zoom interviews or one-on-one interviews.
Interventions
- Behavioral Discussion
Attend focus groups - Other Interview
Attend interviews - Other Survey Administration
Ancillary studies
Primary outcome measures
- Preferences of food and beverage self-monitoring methodology and respective feedback messages [Time frame: Up to 3 years]
Eligibility criteria
Inclusion criteria
- Pasadena Independent School District (ISD) employees who have completed the 6-month Vibrant Lives weight loss program or adults who have completed a weight loss program within the last 12 months
Criteria are shown verbatim from the registry (in English). Final eligibility is always assessed by the study center.
Healthy volunteers: Yes
Study design
- Observational model
- Ecologic or community
Study locations
United States · 1 center
- M D Anderson Cancer Center — Houston
Identifiers
NCT: NCT04611087 · PA18-0407 · NCI-2020-07542 · PA18-0407