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Weight Loss Counseling for African American Women Who Are Breast Cancer Survivors

A Culturally-Tailored Weight Loss Program

Status
Completed
Phases
Unknown
Study type
Observational
Source
ClinicalTrials.gov
Registry ID
NCT00872677
Enrollment
31
Registered
2009-03-31
Start date
2004-05-31
Completion date
2008-11-30
Last updated
2013-04-29

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Breast Cancer, Obesity, Weight Changes

Keywords

weight changes, obesity, stage I breast cancer, stage II breast cancer, stage IIIA breast cancer

Brief summary

RATIONALE: A culturally sensitive weight loss program for obese African American breast cancer survivors may be more effective than a standard weight loss program in helping women lose weight. PURPOSE: This randomized clinical trial is studying personalized weight loss counseling to see how well it works in African American women who are breast cancer survivors.

Detailed description

OBJECTIVES: * To develop a weight loss intervention for obese African American women who are breast cancer survivors. OUTLINE: This is a randomized study. Participants are randomized to 1 of 2 intervention groups. * Group 1: Participants receive traditional individual dietary and exercise counseling in combination with the Weight Watchers weight loss program for 18 months. * Group 2: Participants receive individual dietary and exercise counseling in combination with the Weight Watchers weight loss program as in group 1. They also receive spiritual counseling that incorporates meditation, readings, and the recording of thoughts into a long-term weight management program. The program addresses coping with stress, setting priorities, dealing with emotional issues that trigger old behavior patterns, and developing accountability for following desired diet and exercise patterns.

Interventions

BEHAVIORALDiet

Talk to study dietitian (eight in person or by phone) weekly for the first 3 months, every other week for the next 3 months and monthly thereafter.

OTHERSpiritual counseling

Spiritual counselor weekly in months 6-9, every other week in months 9-12 and monthly thereafter.

Sponsors

National Center for Complementary and Integrative Health (NCCIH)
CollaboratorNIH
National Cancer Institute (NCI)
CollaboratorNIH
Barbara Ann Karmanos Cancer Institute
Lead SponsorOTHER

Study design

Observational model
CASE_CONTROL
Time perspective
PROSPECTIVE

Eligibility

Sex/Gender
FEMALE
Age
18 Years to 70 Years
Healthy volunteers
No

Inclusion criteria

DISEASE CHARACTERISTICS: * Diagnosis of breast cancer within the past 5 years * Stage I-IIIA disease * No recurrence of cancer * Identified as African American * Body Mass Index 30-40 * Hormone receptor status not specified PATIENT CHARACTERISTICS: * Menopausal status not specified * Stable body weight * Not currently following a special diet * No uncontrolled congestive heart failure, untreated hypertension, disabling osteoarthritis, drug or alcohol abuse, or psychiatric conditions that may interfere with counseling PRIOR CONCURRENT THERAPY: * More than 3 months since prior chemotherapy or radiotherapy

Design outcomes

Primary

MeasureTime frame
Weight change18 months

Countries

United States

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 4, 2026