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The Role of a Virtual Coach in Improving Adherence to an Activity Program for Overweight Adults

Not Applicable
Completed
Conditions
Overweight
Interventions
Other: Virtual Coach software
Other: Activity monitor and website
Registration Number
NCT00792207
Lead Sponsor
Massachusetts General Hospital
Brief Summary

Hypothesis: Overweight subjects using a Virtual Coach will demonstrate improved adherence to an exercise regime.

This study is designed to examine the effect of a computer program called a "Virtual Coach" and find out if it helps people become more active. This program acts as a kind of a personal trainer and will give you feedback. All participants in the study will receive an activity monitor to wear during the study and a website to use to track activity. Half of the participants will also receive the virtual coach software. This software will have to be downloaded onto your computer, and we will ask that you check in with the coach using the software three times a week for 12 weeks. The group you will be placed in will be selected by chance.

Detailed Description

Not available

Recruitment & Eligibility

Status
COMPLETED
Sex
All
Target Recruitment
70
Inclusion Criteria
  • Adults age 20-55 inclusive
  • BMI between 25 and 35 inclusive (overweight and Class 1 obese subjects)
  • PC Computer with an available USB port, speakers and high-speed internet access in a secure setting (home or private office)
  • Fluency in English (spoken and written)
  • Have a Primary Care Physician
  • Answer "No" to all 7 questions on PAR-Q OR have letter from PCP clearing them to take part in study
Exclusion Criteria
  • Disability, medical or surgical condition preventing or precluding moderate physical activity.
  • Cognitive impairment.

Study & Design

Study Type
INTERVENTIONAL
Study Design
PARALLEL
Arm && Interventions
GroupInterventionDescription
InterventionVirtual Coach softwareIntervention Group: The intervention being tested, the Virtual Coach, is an automated empathic computer agent which will run on patient's home computer and engage the patient in dialogues to deliver personalized feedback, education and coaching based on physiological data recorded by an activity monitor.
ControlActivity monitor and websiteThe control group will use an activity monitor and will have access to a website to monitor activity, but will not receive the Virtual Coach program.
Primary Outcome Measures
NameTimeMethod
The primary outcome being measured is the level of activity monitored by the activity monitor. Control and Intervention subjects will be encouraged to wear the activity monitor on a daily basis for the 12 week course of the study.12 weeks
Secondary Outcome Measures
NameTimeMethod
Change in subject waist circumference. Subjects will be measured at their first study visit and their final visit12 weeks
Changes in self-efficacy, quality of or readiness to change (as measured through surveys at the beginning and end of the study).12 weeks
Change in subject weight. Subjects will be weighed at their first study visit and their final visit.12 weeks
Subject rating on the working alliance inventory score12 weeks, assessed at the end of the study

Trial Locations

Locations (1)

Partners Health Care Center for Connected Health

🇺🇸

Boston, Massachusetts, United States

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