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


N/A
25 Years
65 Years
Not Enrolling
Both
Obesity

Thank you

Trial Information

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


- 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.


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

Type of Study:

Interventional

Study Design:

Allocation: Randomized, Endpoint Classification: Efficacy Study, Intervention Model: Parallel Assignment, Masking: Open Label, Primary Purpose: Supportive Care

Outcome Measure:

Weight

Outcome Time Frame:

24 weeks

Safety Issue:

No

Principal Investigator

Gary Bennett, Ph.D

Investigator Role:

Principal Investigator

Investigator Affiliation:

Dana-Farber Cancer Institute

Authority:

United States: Institutional Review Board

Study ID:

06-007

NCT ID:

NCT00644202

Start Date:

May 2006

Completion Date:

February 2007

Related Keywords:

  • Obesity
  • weight control
  • Obesity

Name

Location

Dana-Farber Cancer Institute Boston, Massachusetts  02115
Department of Ambulatory Care and Prevention Boston, Massachusetts  02215