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Completed

NCT Number: NCT00583726

The Women's Healthy Lifestyle Study

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

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Key information

Age range

18 year–99 year

Sex eligibility

Female

Study type

Interventional

Phase

Not applicable

Primary location

University of Michigan

Ann Arbor, Michigan, 48109, United States

About this study

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.

Who can participate

Healthy volunteers accepted: No

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

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 25-45 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

Treatment and study plan

Motivational Interviewing

Behavioral

telephone counseling

written materials only

Behavioral

dietary guidance materials and pedometers

Primary outcomes

  1. Change in body weight

    Time frame: 12 months

Secondary outcomes

  1. Change in body fat

    Time frame: 12 months

Sponsors and collaborators

Lead sponsor

University of Michigan

Other

Registry information

Official study title

Motivational Interviewing for Weight Maintenance

Important dates

Study start
2007
Primary completion
2010
Study completion
2011
First posted
Dec 31, 2007
Registry last updated
Dec 2, 2015

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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