Clinical Trials Directory

Trials / Terminated

TerminatedNCT00641849

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

Status
Terminated
Phase
N/A
Study type
Interventional
Enrollment
54 (actual)
Sponsor
University of Missouri-Columbia · Academic / Other
Sex
All
Age
18 Years – 80 Years
Healthy volunteers
Accepted

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.

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emails will also state that those subjects not completing their "follow-up" visit within the visit window will be withdrawn from the study.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.

Conditions

Interventions

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

Timeline

Start date
2008-07-01
Primary completion
2010-04-01
Completion
2010-04-01
First posted
2008-03-24
Last updated
2016-10-04

Locations

2 sites across 1 country: United States

Source: ClinicalTrials.gov record NCT00641849. Inclusion in this directory is not an endorsement.