Compliance: Physical Activity and Dietary Behaviors of Adults 18 to 80 Years of Age

Sponsor
University of Missouri-Columbia (Other)
Overall Status
Terminated
CT.gov ID
NCT00641849
Collaborator
Northern Arizona University (Other)
54
2
2
21
27
1.3

Study Details

Study Description

Brief Summary

This research will focus on the effect of a 6-month behavioral intervention delivered via the World Wide Web that is aimed at increasing physical activity levels and decreasing dietary fat intake in a general population of adults. The study will be randomized and blinded. We are also planning to study subjects' compliance and retention rates when enrolled in a completely on-line study.

Condition or Disease Intervention/Treatment Phase
  • Behavioral: Group A
  • Behavioral: Group B
N/A

Detailed Description

The research is designed as a prospective multi-site, randomized, blinded trial.

Participants will fill out an initial questionnaire 72 hours (time 0) after completing the inclusion/exclusion questionnaire and consent documents. An email will be sent sixty (60) hours after participants who agreed to the online consent and HIPAA articles. Subjects who have consented to participate in the trial will not be considered as enrolled until after they have completed their time 0 data forms and completed the education module.

The subjects will be randomly assigned to either the minimum or maximum treatment group. Both groups will be sent an email reminder 7 days prior to their "follow-up" date. They will then be sent an email reminder 24 hours prior to their "follow-up" date. Subjects will receive an email reminder every 48 hours until 336 hours (14 days) post visit date. Reminder emails will also state that those subjects not completing their "follow-up" visit within the visit window will be withdrawn from the study. Subjects will be not be blinded as to how frequently they will be required to make "follow-up" visits to the site.

Group A: Minimum Intervention Group A will fill out data forms at zero (0), two (2), four (4), and six (6) months.

Group B: Maximum Intervention Group B will fill out data forms at zero (0), one (1), two (2), three (3), four (4), five (5), and six (6) months.

A short online education module will be given after the initial surveys (time 0) have been completed by the study subject. They will receive their initial "feedback" letter after completing the education module. It will also tell them the date of their "follow-up" visit, and that they will be periodically prompted to return to the site and complete a questionnaire.

Both groups will receive a "feedback" letter upon completion of each online "follow-up" visit. This letter will give them "feedback" based off of how they answered their data forms. All "feedback" given will be based off of established recommended physical activity and the USDA food pyramid guidelines. The BMI will be calculated; BMI = weight (kg)/height2 (m2).

Subjects in both groups who have not completed their "follow-up" visits after 336 hours (14 days) post visit date will be sent an email notifying them that they have been dropped from the study.

Study Design

Study Type:
Interventional
Actual Enrollment :
54 participants
Allocation:
Randomized
Intervention Model:
Parallel Assignment
Masking:
Single (Investigator)
Primary Purpose:
Supportive Care
Official Title:
Physical Activity and Dietary Behaviors of Adults 18 to 80 Years of Age
Study Start Date :
Jul 1, 2008
Actual Primary Completion Date :
Apr 1, 2010
Actual Study Completion Date :
Apr 1, 2010

Arms and Interventions

Arm Intervention/Treatment
Active Comparator: Group A

Minimum Intervention Group A will fill out data forms at zero (0), two (2), four (4), and six (6) months.

Behavioral: Group A
Minimum Intervention Group A will fill out data forms at zero (0), two (2), four (4), and six (6) months.
Other Names:
  • Minimal intervention
  • Active Comparator: Group B

    Maximum Intervention Group B will fill out data forms at zero (0), one (1), two (2), three (3), four (4), five (5), and six (6) months.

    Behavioral: Group B
    Maximum Intervention Group B will fill out data forms at zero (0), one (1), two (2), three (3), four (4), five (5), and six (6) months.
    Other Names:
  • Maximum intervention
  • Outcome Measures

    Primary Outcome Measures

    1. Comparison of the level of compliance and retention between the two groups. [Six months]

    Secondary Outcome Measures

    1. Mean physical activity levels of trial completers relative to their mean baseline PA levels. [Six months]

    2. Mean fat intake score of trial completers relative to their mean baseline fat intake. [Six months]

    3. Mean body mass index (BM) of trial completers relative to their mean baseline BMI. [Six Months]

    4. Comparison of mean physical activity level, fat intake scores, and BMI of trial completers in each treatment arm at 6 months (outcome means adjusted for baseline values). [Six months]

    5. Changes in PA levels, fat intake scores and BMI over time for subjects in each treatment arm. [Six months]

    6. Intent-to treat analysis will be conducted at outcome for physical activity, fat intake scores and BMI by carrying the last entered values forward to represent the values at outcome. Intent to treat analysis may be precluded by a high dropout rate. [Six months]

    7. Subject reported satisfaction with participation in an on-line study [Six months]

    Eligibility Criteria

    Criteria

    Ages Eligible for Study:
    18 Years to 80 Years
    Sexes Eligible for Study:
    All
    Accepts Healthy Volunteers:
    Yes
    Inclusion Criteria:
    • Adults 18 years to 80 years

    • Participants must be willing to complete initial questionnaire 72 hours after completing inclusion criteria screening and review of informed consent

    • Participants must be willing to review educational module

    • Participants must be willing to fill out seven (7) questionnaires per protocol.

    Exclusion Criteria:

    -Individuals who do not have access to the Internet

    Contacts and Locations

    Locations

    Site City State Country Postal Code
    1 Northern Arizona University Flagstaff Arizona United States 86011-5066
    2 University of Missouri Columbia Missouri United States 65212

    Sponsors and Collaborators

    • University of Missouri-Columbia
    • Northern Arizona University

    Investigators

    • Principal Investigator: Pamela S Cooper, PhD, University of Missouri-Columbia

    Study Documents (Full-Text)

    None provided.

    More Information

    Additional Information:

    Publications

    Responsible Party:
    University of Missouri-Columbia
    ClinicalTrials.gov Identifier:
    NCT00641849
    Other Study ID Numbers:
    • 1103057
    First Posted:
    Mar 24, 2008
    Last Update Posted:
    Oct 4, 2016
    Last Verified:
    Oct 1, 2016
    Individual Participant Data (IPD) Sharing Statement:
    No
    Plan to Share IPD:
    No
    Keywords provided by University of Missouri-Columbia

    Study Results

    No Results Posted as of Oct 4, 2016