Weight Control Programs in Women Who Have Undergone Surgery for Early Stage Breast Cancer

B- AHEAD Study (Breast - Activity & Healthy Eating After Diagnosis) Randomised Comparison of 3 Weight Control Programmes During Adjuvant Treatment for Early Breast Cancer.

RATIONALE: Measuring changes in body weight and body composition in women with early-stage breast cancer may help doctors plan the best weight control program and improve patients' quality of life. It is not yet known which program is most effective in women with breast cancer.

PURPOSE: This randomized clinical trial is comparing three weight control programs to see how well they work in women who have undergone surgery for early stage breast cancer.

Study Overview

• Status: Completed
• Conditions: Breast Cancer; Weight Changes
• Intervention / Treatment: Other: laboratory biomarker analysis; Other: questionnaire administration; Procedure: support group therapy; Procedure: quality-of-life assessment; Other: educational intervention; Other: counseling intervention; Behavioral: behavioral dietary intervention; Behavioral: exercise intervention

Detailed Description

OBJECTIVES:

Primary

• To assess changes in body weight and composition (i.e., body fat, fat-free mass, dual energy x-ray absorptiometry, bioelectrical impedance, and waist and hip circumference) in patients with early stage breast cancer.

Secondary

• To assess uptake and retention to the interventions and adverse effects of the interventions in these patients.

OUTLINE: This is a multicenter study.

Patients are stratified according to adjuvant treatment (chemotherapy vs no chemotherapy), body mass index (> 27kg/m² vs < 27 kg/m²), treating hospital (UHSM vs North Manchester vs Royal Oldham vs Stepping Hill Hospital), high vs low risk of reducing bone density (i.e., patients receiving aromatase inhibitors vs premenopausal women receiving chemotherapy and/or tamoxifen vs postmenopausal women receiving tamoxifen), and high vs low risk of developing lymphedema (i.e., axillary node clearance vs no axillary node clearance). Patients are randomized to 1 of 3 interventions.

• Arm I: Patients receive standard written advice "Healthy Living With Breast Cancer" booklet from South Manchester University Hospital.
• Arm II: Patients receive individualized diet and exercise advice from a study dietitian for 40 minutes and from the exercise referral officer for 40 minutes. Advice is reinforced with 20-minute bi-weekly phone calls checking compliance, changes in diet, physical activity, individual problems and goals, and recommendations. Patients also receive mailed information summarizing key motivational, behavioral, diet, and exercise issues; information covered in group sessions on weight management; and a booklet providing a program of walking, strengthening, toning, and flexibility exercises.
• Arm III: Patients undergo a supervised group community weight control intervention based on Courneya's exercise prescription guidelines for breast cancer patients and survivors. The intervention consists of a 5-minute warm-up comprising walking and movement to music, 20-30 minutes of circuit training with approximately 10 stations incorporating aerobic activities (i.e., brisk walking, cycling, low-level exercise to music) and muscle strengthening activities (i.e., wall press-up, side leg raises, light weights, and resistance bands), 10-minute cool-down with stretch and flexibility exercises, and 5-minute relaxation period. Patients also undergo a 30-minute diet and behavior change educational session based on the trans theoretical model of behavior changes. The intervention repeats once weekly for 12 weeks. Patients receive a booklet providing a program of walking, strengthening, toning, and flexibility exercises. Patients also receive booster phone calls to reinforce advice, problem solve, and monitor compliance at 4, 6, and 9 months.

In all arms, quality of life is assessed at baseline and 3, 6, and 12 months. Serum bone markers, insulin, glucose, and cardiovascular disease markers are measured periodically.

• Study Type: Observational
• Enrollment (Actual): 409

Contacts and Locations

Study Locations

• United Kingdom
  • England
    • Manchester, England, United Kingdom, M20 4BX
      • Christie Hospital
    • Manchester, England, United Kingdom, M23 9LT
      • South Manchester University Hospital
    • Manchester, England, United Kingdom, M13 9WL
      • Wellcome Trust Clinical Research Facility
    • Manchester, England, United Kingdom, M23 9LT
      • Nightingale Centre and Genesis Prevention Centre at Wythenshawe Hospital
    • Stirling, England, United Kingdom, FK9 4NF
      • Cancer Care Research Centre at University of Stirling

Participation Criteria

Eligibility Criteria

• Ages Eligible for Study: 18 years and older (Adult, Older Adult)
• Accepts Healthy Volunteers: No
• Genders Eligible for Study: Female

Description

DISEASE CHARACTERISTICS:

• Diagnosis of early breast cancer

  • Stage I-III disease
  • Invasive or in situ disease
• No metastatic or inoperable disease
• Underwent primary surgery for primary breast cancer at UHSM, North Manchester, Royal Oldham, Stepping Hill, Hope Macclesfield General, Tameside General, Leighton Hospitals, or Rochdale Infirmary within the past 10 weeks
• Receiving/due to start adjuvant chemotherapy, radiotherapy, endocrine therapy, or no adjuvant treatment
• Hormonal receptor status not specified

PATIENT CHARACTERISTICS:

• Pre or postmenopausal status
• Any weight allowed
• Resident within Greater Manchester or Cheshire area

• No physical/psychiatric condition that impairs compliance or mobility as assessed from medical history or baseline fitness assessment, including any of the following:

  • Insulin-requiring diabetes (non-insulin requiring diabetics are eligible)
  • Serious digestive and/or absorptive problems, including inflammatory bowel disease
  • Cardiovascular or respiratory disease
  • Musculoskeletal disease or joint problems
  • Psychiatric disorders or conditions (e.g., untreated major depression, psychosis, substance abuse, or severe personality disorder)
• Not considering reconstructive surgery in the next 12 months

PRIOR CONCURRENT THERAPY:

• See Disease Characteristics

• No concurrent daily medication known to affect body composition (e.g., corticosteroids)

  • Patients receiving 2-3 days of steroids with chemotherapy are eligible
• No prior neoadjuvant chemotherapy or endocrine therapy

Study Plan

How is the study designed?

What is the study measuring?

Primary Outcome Measures

Outcome Measure
Changes in body weight and composition (i.e., body fat, fat-free mass, dual energy x-ray absorptiometry, bioelectrical impedance, and waist and hip circumference) at baseline and at 6 and 12 months

Secondary Outcome Measures

Outcome Measure
Uptake and retention of information about the interventions and adverse effects of the interventions
Changes in quality of life as assessed by FACT-B, B-ES, and -F at baseline and at 6 and 12 months
Changes in markers of breast cancer prognosis at baseline and at 6 and 12 months
Changes in insulin resistance and glucose homeostasis model assessment (HOMA) at baseline and at 6 and 12 months
Cardiovascular disease-risk markers (i.e., total LDL and HDL cholesterol, triglycerides, and systolic/diastolic blood pressure) at baseline and at 6 and 12 months
Changes in fitness as assessed by a 12-minute walk test at baseline and at 6 and 12 months
Changes in arm mobility, function (as assessed by quick DASH), and pain (as assessed by pain rating scale and S-LANSS for neuropathic pain) at baseline and at 6 and 12 months
Changes in dietary intake (as assessed by a 7-day food diary) and activity (as assessed by a 7-day activity diary) as measures of compliance at baseline and at 6 and 12 months
Changes in serum bone markers/bone specific alkaline phosphatase for bone formation and the cross linked C-telopeptides of type I collagen for bone resorption at baseline and at 6 and 12 months
Changes in ipsilateral arm circumference (compared to contralateral arm) using perometer in patients having axillary node clearance at baseline and at 6 and 12 months
Changes in generic health status and quality of life (as assessed by EQ-5D utility measure) and health resource usage to assess the relative cost effectiveness of the interventions at baseline and at 3, 6, and 12 months
Changes in isometric and isokinetic muscle strength of quadriceps in patients receiving aromatase inhibitors and age-matched patients receiving tamoxifen in a subset of patients in the standard written only group
Patient experience of interventions through in-depth focus group discussions and individual interviews
Factors predicting adherence to interventions with scales of stage of behavior change for weight control and exercise

Collaborators and Investigators

• Sponsor: Wythenshawe Hospital
• Investigators: Principal Investigator: Michelle Harvie, MD, Wythenshawe Hospital

Study record dates

Study Major Dates

• Study Start: August 1, 2008
• Study Completion (Actual): February 1, 2011

Study Registration Dates

• First Submitted: March 25, 2009
• First Submitted That Met QC Criteria: March 25, 2009
• First Posted (Estimate): March 26, 2009

Study Record Updates

• Last Update Posted (Estimate): April 4, 2013
• Last Update Submitted That Met QC Criteria: April 2, 2013
• Last Verified: March 1, 2009

More Information

Terms related to this study

• Keywords: stage IIIA breast cancer; stage IIIB breast cancer; stage II breast cancer; stage IIIC breast cancer; stage IA breast cancer; stage IB breast cancer; weight changes
• Additional Relevant MeSH Terms: Skin Diseases; Neoplasms; Neoplasms by Site; Breast Diseases; Breast Neoplasms; Body Weight; Body Weight Changes
• Other Study ID Numbers: NCGPC-B-AHEAD; CDR0000633348 (Registry Identifier: PDQ (Physician Data Query)); EU-20906