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NCT04611087 Clinical Trial

Self-monitoring Focus Groups With Vibrant Lives Pasadena Participants

Obesity-Related Malignant Neoplasm Clinical Trial

Official title:
Self-Monitoring Focus Groups With Vibrant Lives Pasadena Participants

Clinical Trial Details — Status: Recruiting

Administrative data
NCT number NCT04611087
Other study ID # PA18-0407
Secondary ID NCI-2020-07542PA
Status Recruiting
Phase
First received
Last updated
Start date July 3, 2018
Est. completion date April 30, 2025

Study information
Verified date February 2024
Source M.D. Anderson Cancer Center
Contact Karen M Basen-Engquist
Phone 713-745-3123
Email kbasenen@mdanderson.org
Is FDA regulated No
Health authority
Study type Observational

Clinical Trial Summary

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.

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.

Recruitment information / eligibility
Status Recruiting
Enrollment 39
Est. completion date April 30, 2025
Est. primary completion date April 30, 2025
Accepts healthy volunteers Accepts Healthy Volunteers
Gender All
Age group N/A and older
Eligibility 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

Study Design

Related Conditions & MeSH terms

  • Neoplasms
  • Obesity-Related Malignant Neoplasm

Intervention

Behavioral:
• Discussion
Attend focus groups
Other:
• Interview
Attend interviews
• Survey Administration
Ancillary studies

Locations
Country Name City State
United States M D Anderson Cancer Center Houston Texas

Sponsors (1)
Lead Sponsor Collaborator
M.D. Anderson Cancer Center

Country where clinical trial is conducted

United States, 

Outcome
Type Measure Description Time frame Safety issue
Primary Preferences of food and beverage self-monitoring methodology and respective feedback messages Thematic and narrative analyses will be conducted from the transcriptions to gain an understanding for the preferences of food and beverage self-monitoring methodology and respective feedback messages. Up to 3 years
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