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OpenTrials
Completed

NCT Number: NCT00644202

A Pilot Weight Control Intervention at HPHC

The purpose of this study is to examine how adults can improve their physical activity levels and eating habits using an interactive web-based weight control program and regular contact with a dietician.

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Key information

Age range

25 year–65 year

Sex eligibility

All sexes

Study type

Interventional

Phase

Not applicable

Primary location

Dana-Farber Cancer Institute, Boston, Massachusetts, United States

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About this study

  • All study participants must have regular access to the Internet, however, the study will not provide this access. Participants will be randomly placed in one of two study groups (Group 1 or Group 2).
  • Group 1 participants will be asked to make 3 in-person visits, each lasting 75-90 minutes. The following information will be collected: name, mailing address, telephone number, and email address. During the study visit, the following measurements will be taken: height, weight, waist circumference, blood pressure and dietary patterns.
  • Group 1 participants will also receive counseling around diet and physical activity from a registered dietician and be asked to use a specialized website that will allow them to track eating and physical activity patterns, learn new weight management skills, interact with the dietician, and receive support from other participants.
  • Group 1 will also receive 5 telephone counseling calls with a health counselor. During the telephone calls, we will teach the participant new skills such as tracking diet and physical activity, goal-setting and staying motivated.
  • Group 2 participants will be asked to make 2 in-person visits, each lasting 75-90 minutes in length. The following information will be collected: your name, mailing address, and telephone number. During the study visit, the following measurements will be taken: height, weight, waist circumference, blood pressure and dietary patterns.

Who can participate

Healthy volunteers accepted: No

Only the study team can determine whether someone qualifies for participation.

Inclusion criteria

  • 25 to 65 years of age
  • Body mass index between 30-40 kg/m2
  • Non-smoker (quit within previous 6 months)
  • Comfort reading and speaking English
  • Stage 1 hypertension
  • Not currently pregnant
  • Regular web access from home

Treatment and study plan

Counseling Sessions

Behavioral

Counseling Sessions at each study visit around diet and physical activity from a registered dietician

Specialized Website

Behavioral

Specialized website that allows participants to track their eating and physical activity patterns, learn new weight management skills, interact with the dietician, and receive support from other participants

Telephone Counseling Calls

Behavioral

5 telephone calls with a health counselor, lasting 15-20 minutes each.

Primary outcomes

  1. Weight

    Time frame: 24 weeks

Secondary outcomes

  1. Blood pressure

    Time frame: 24 weeks

  2. Diet

    Time frame: 24 weeks

  3. Physical activity

    Time frame: 24 weeks

Sponsors and collaborators

Lead sponsor

Dana-Farber Cancer Institute

Other

Collaborators

  • Harvard Pilgrim Health Care

Registry information

Official study title

A Pilot Weight Control Intervention at Harvard Pilgrim Health Care (HPHC)

Important dates

Study start
2006
Primary completion
2007
Study completion
2007
First posted
Mar 26, 2008
Registry last updated
Mar 26, 2008

OpenTrials presents study information sourced from ClinicalTrials.gov. The official registry record should be consulted for the latest information.

View the official ClinicalTrials.gov record (opens in a new tab)

This listing is for discovery and informational purposes only. It is not medical advice, does not guarantee that a study is recruiting, and does not determine eligibility. Contact the study team and a qualified healthcare professional when considering participation.

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