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Self-monitoring Focus Groups With Vibrant Lives Pasadena Participants

Sponsor
M.D. Anderson Cancer Center (Other)
Overall Status
Recruiting
CT.gov ID
NCT04611087
Collaborator
(none)
39
Enrollment
1
Location
50
Anticipated Duration (Months)
0.8
Patients Per Site Per Month

Study Details

Study Description

Brief 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.

Condition or Disease Intervention/Treatment Phase
  • Behavioral: Discussion
  • Other: Interview
  • Other: Survey Administration

Detailed Description

PRIMARY OBJECTIVE:
  1. 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.

Study Design

Study Type:
Observational
Anticipated Enrollment :
39 participants
Observational Model:
Ecologic or Community
Time Perspective:
Cross-Sectional
Official Title:
Self-Monitoring Focus Groups With Vibrant Lives Pasadena Participants
Actual Study Start Date :
Jul 3, 2018
Anticipated Primary Completion Date :
Sep 1, 2022
Anticipated Study Completion Date :
Sep 1, 2022

Arms and Interventions

Arm Intervention/Treatment
Observational (focus group, interview)

PHASE I: Participants attend 4 sessions of focus groups. PHASE II: Participants attend virtual Zoom interviews or one-on-one interviews.

Behavioral: Discussion
Attend focus groups
Other Names:
  • Discuss

    • Other: Interview
    Attend interviews

    Other: Survey Administration
    Ancillary studies

    Outcome Measures

    Primary Outcome Measures

    1. Preferences of food and beverage self-monitoring methodology and respective feedback messages [Up to 3 years]

      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.

    Eligibility Criteria

    Criteria

    Ages Eligible for Study:
    N/A and Older
    Sexes Eligible for Study:
    All
    Accepts Healthy Volunteers:
    Yes
    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

    Contacts and Locations

    Locations

    Site City State Country Postal Code
    1 M D Anderson Cancer Center Houston Texas United States 77030

    Sponsors and Collaborators

    • M.D. Anderson Cancer Center

    Investigators

    • Principal Investigator: Karen M Basen-Engquist, M.D. Anderson Cancer Center

    Study Documents (Full-Text)

    None provided.

    More Information

    Additional Information:

    Publications

    None provided.
    Responsible Party:
    M.D. Anderson Cancer Center
    ClinicalTrials.gov Identifier:
    NCT04611087
    Other Study ID Numbers:
    • PA18-0407
    • NCI-2020-07542
    • PA18-0407
    First Posted:
    Nov 2, 2020
    Last Update Posted:
    Feb 2, 2022
    Last Verified:
    Jan 1, 2022
    Studies a U.S. FDA-regulated Drug Product:
    No
    Studies a U.S. FDA-regulated Device Product:
    No
    Additional relevant MeSH terms:
    Neoplasms

    Study Results

    No Results Posted as of Feb 2, 2022