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The Women's Healthy Lifestyle Study

This study is currently recruiting participants.
Verified by University of Michigan, June 2008

Sponsored by: University of Michigan
Information provided by: University of Michigan
ClinicalTrials.gov Identifier: NCT00583726
  Purpose

This study aims to determine if a motivational interviewing counseling style can help women eat a healthy diet and exercise during breast canecr treatment and beyond.


Condition Intervention
Breast Cancer
Behavioral: motivational interviewing
Behavioral: written materials only

Genetics Home Reference related topics:   breast cancer   

MedlinePlus related topics:   Breast Cancer    Cancer    Exercise and Physical Fitness   

U.S. FDA Resources

Study Type:   Interventional
Study Design:   Supportive Care, Randomized, Open Label, Dose Comparison, Parallel Assignment, Efficacy Study
Official Title:   Motivational Interviewing for Weight Maintenance

Further study details as provided by University of Michigan:

Primary Outcome Measures:
  • chnage in body weight [ Time Frame: 12 months ] [ Designated as safety issue: No ]

Secondary Outcome Measures:
  • change in body fat [ Time Frame: 12 months ] [ Designated as safety issue: No ]

Estimated Enrollment:   40
Study Start Date:   December 2007
Estimated Study Completion Date:   November 2010
Estimated Primary Completion Date:   August 2010 (Final data collection date for primary outcome measure)

Arms Assigned Interventions
1: Active Comparator
The control arm receives written information and pedometers
Behavioral: written materials only
dietary guidenace materials and pedometers
2: Experimental
This arm also receives telephone counseling.
Behavioral: motivational interviewing
telephone counseling

Detailed Description:

Women receiving chemotherapy for early stage breast cancer often gain weight and body fat, and this contributes to the health burden that cancer survivors face. Weight gain is a concern not only for overall health status, but also as a possible factor for risk of cancer recurrence. Unfortunately achieving weight loss, after a gain has occurred, is difficult, and there are no satisfactory methods for maintenance of weight loss. This study proposes to design and test a novel telephone-based intervention for preventing weight gain during treatment for breast cancer in a pilot, randomized study. The 12-month intervention will target maintenance of current weight and prevention of body fat gain using counseling for moderate exercise and a low-fat, high fruit-vegetable diet. The counseling approach will be based on motivational interviewing techniques and will be delivered through telephone appointments. Motivational interviewing is a client-centered type of counseling that elicits active participation of the patient. By taking a more active role, patients may be more likely to follow through with the recommended lifestyle changes. Study endpoints will include blood markers of dietary compliance, pedometer steps, self-monitoring logs, questionnaires (including quality of life) and anthropometric measures (including body fat by DEXA). An important goal of the study is to establish recruitment methods and demonstrate recruitment rates in newly diagnosed stage I-IIIA breast cancer patients. The study data also will demonstrate implementation of the counseling approach and provide a basis for sample size estimates for a larger trial. This type of intervention, namely a combination of exercise and diet, has been indicated to have good potential for prevention of recurrence. It is therefore necessary to develop effective methods for eliciting these behaviors.

  Eligibility
Ages Eligible for Study:   18 Years and older
Genders Eligible for Study:   Female
Accepts Healthy Volunteers:   No

Criteria

Inclusion Criteria:

  • Adult female, age 18 and older
  • Stage I, II, or IIIA breast cancer
  • Scheduled for chemotherapy and completed no more than two weeks of chemotherapy
  • Body mass index 25-40 kg/m2
  • Stable body weight within 5 pounds in the past 2 months
  • Physician approval for participating in a weight control program
  • Willing and able to follow advice for exercise and diet quality

Exclusion Criteria:

  • Previous invasive cancers, excluding basal cell carcinoma, in the past 10 years
  • Following a medically-prescribed diet
  • Currently participating in a formal weight loss program
  • Medical conditions that preclude safe exercise
  Contacts and Locations

Please refer to this study by its ClinicalTrials.gov identifier: NCT00583726

Contacts
Contact: Jennifer Ellsworth, RD, MS     7346154844     jennells@umich.edu    
Contact: Zora Djuric, PhD     7346156210     zoralong@umich.edu    

Locations
United States, Michigan
University of Michigan     Recruiting
      Ann Arbor, Michigan, United States, 48109

Sponsors and Collaborators
University of Michigan

Investigators
Principal Investigator:     Zora Djuric, PhD     University of Michigan    
  More Information


Responsible Party:   Unviesrity of Michigan ( Dr. Zora Djuric )
Study ID Numbers:   HUM00012524
First Received:   December 20, 2007
Last Updated:   June 9, 2008
ClinicalTrials.gov Identifier:   NCT00583726
Health Authority:   United States: Institutional Review Board

Keywords provided by University of Michigan:
chemotherapy  
exercise  
diet  
fruit
vegetables
low-fat

Study placed in the following topic categories:
Body Weight
Skin Diseases
Breast Neoplasms
Healthy
Breast Diseases

Additional relevant MeSH terms:
Neoplasms
Neoplasms by Site

ClinicalTrials.gov processed this record on October 31, 2008




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