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Automated Guidance Tool for Medical Encounters Addressing Therapeutic Lifestyle Changes (AuGMEnT).
This study is ongoing, but not recruiting participants.
Sponsored by: Griffin Hospital
Information provided by: Griffin Hospital
ClinicalTrials.gov Identifier: NCT00790491
  Purpose

ABSTRACT Although most primary healthcare practitioners recognize the important relationship among nutrition, physical activity and health, few incorporate either dietary or physical activity counseling into routine practice. AUGMENT will employ interactive technology to support effective patient life-style counseling during routine office visits. AUGMENT technology will automate the administration, collection, and analysis of dietary and physical activity questionnaires, and it will guide counseling and present intervention resources and strategies tailored to the patient's unique needs. Using tablet computers, wireless LANs, and inexpensive Internet communications, AUGMENT will have advantages over existing tools: 1.) Lower usage costs (minimal office personal required), 2.) Ability to customize the system, and 3.) Real-time, comprehensive assessment.

The AUGMENT system efficiently and relentlessly gathers important healthcare information (such as total fat, type of fat consumption; fruit and vegetable consumption; fiber and micronutrient intake; and energy output). This means patients are less likely to have their preventive needs overlooked by a busy practitioner. The assessment includes questions to determine the amount of effort the patient will commit to improved health. This will enable the physician to effectively guide the patient via targeted recommendations, obtainable goals, and a course of action that is both preventive and prescriptive; and to monitor progress. Patients who receive objective assessments of their healthcare practices and recommendations based on their own unique health history will be more likely to accept and act on the recommendations.

The specific aims of the study are to: 1) Incorporate key elements of a previously developed prototype tool into a dietary and physical activity risk assessment system, 2) Create a provider training tool to build proficiency in using AUGMENT for counseling to reduce disease risk.

3) Validate the AUGMENT dietary and physical activity assessments using dietary recalls and accelerometer data, 4) Complete a process evaluation of the AUGMENT program by using it in interventions managed by six physicians with at least 240 patients, and 5) Survey participating providers and patients to assess acceptability of AUGMENT within a clinical setting.


Condition Intervention
Heart Disease
Diabetes
Behavioral: guidance tool for providers for lifestyle changes

MedlinePlus related topics: Diabetes Heart Diseases
U.S. FDA Resources
Study Type: Interventional
Study Design: Prevention, Non-Randomized, Open Label, Single Group Assignment
Official Title: Automated Guidance Tool for Medical Encounters Addressing Therapeutic Lifestyle Changes (AuGMEnT)

Further study details as provided by Griffin Hospital:

Primary Outcome Measures:
  • Validate the AUGMENT dietary and physical activity assessments using dietary recalls and accelerometer data, [ Time Frame: 2 years ] [ Designated as safety issue: No ]

Secondary Outcome Measures:
  • Survey participating providers and patients to assess acceptability of AUGMENT within a clinical setting. [ Time Frame: 2 years ] [ Designated as safety issue: No ]

Estimated Enrollment: 240
Study Start Date: October 2007
Estimated Primary Completion Date: October 2009 (Final data collection date for primary outcome measure)
Arms Assigned Interventions
Lifestyle counseling: Experimental Behavioral: guidance tool for providers for lifestyle changes
automated guidance tool for medical providers involved in patient encounters addressing lifestyle changes. Addresses dietary and physical activity. Seeks to reduce cardiac disease risk.

  Eligibility

Ages Eligible for Study:   18 Years and older
Genders Eligible for Study:   Both
Accepts Healthy Volunteers:   No
Criteria

Inclusion Criteria:

  • adult patients at Staywell Community Health Center, Waterbury CT

Exclusion Criteria:

  • terminally ill
  • pregnant women
  • children
  • decisionally impaired / dementia
  Contacts and Locations
Please refer to this study by its ClinicalTrials.gov identifier: NCT00790491

Locations
United States, Connecticut
Greater Waterbury Management Resources and Family Care
Waterbury, Connecticut, United States, 06702
Sponsors and Collaborators
Griffin Hospital
  More Information

Responsible Party: Viocare, Inc ( Rick Weiss )
Study ID Numbers: 2007-11
Study First Received: November 11, 2008
Last Updated: November 12, 2008
ClinicalTrials.gov Identifier: NCT00790491  
Health Authority: United States: Institutional Review Board

Keywords provided by Griffin Hospital:
reduction in risk of heart disease and diabetes

Study placed in the following topic categories:
Heart Diseases
Diabetes Mellitus

Additional relevant MeSH terms:
Cardiovascular Diseases

ClinicalTrials.gov processed this record on January 16, 2009