Effects of Exercise Intervention on Insulin Levels in Breast Cancer Survivors

Breast Cancer Clinical Trial

Official title:

Pilot Study of the Effects of an Exercise Intervention on Insulin Levels in Breast Cancer Survivors

Clinical Trial Details — Status: Completed

Administrative data

• NCT number: NCT00153894
• Other study ID #: 03-327
• Status: Completed
• Phase: N/A
• First received: September 8, 2005
• Last updated: June 24, 2016
• Start date: December 2003
• Est. completion date: February 2008

Study information

• Verified date: June 2016
• Source: Dana-Farber Cancer Institute
• Contact: n/a
• Is FDA regulated: No
• Health authority: United States: Institutional Review Board
• Study type: Interventional

Clinical Trial Summary

The purpose of this study is to determine whether an exercise program comprised of strength and endurance training will lower fasting insulin levels in a group of breast cancer survivors. Insulin may be involved in the risk of breast cancer recurrence.

Description:

• All women taking part in this study will take part in an exercise program. Group A will start exercising immediately and Group B wil have a delay period of 16 weeks before starting to exercise so investigators can look at the changes in insulin levels that occur in a women who is not exercising.

• The exercise program will be made up of two parts: strength (or weight) training and cardiovascular exercise. The strength exercise will take place at a gym close to Dana-Farber Cancer Institute. Patients will work one on one with a personal trainer twice a week for 50 minutes. During each of these sessions, participants will have a brief warm up period and then will perform a series of Nautilus machine-based exercises under the guidance of the personal trainer. The goal of each session will be to increase strength by increasing weight lifted and repetitions.

• Participants will also do cardiovascular exercises on their own at home. Each participant will receive a pedometer and heart rate monitor. Women will be advised to exercise for at least 30 minutes three times per week on their own and will keep a journal recording how long and how intensively they exercised. Participants will receive weekly phone calls from the project manager to review the cardiovascular exercise.

• Women will undergo a series of measurements before and after the 16 week exercise intervention. They will be asked to fast for 12 hours prior to each of these measurement sessions. Measurements will include blood testing for insulin and glucose levels. Women will also be weighed, height will be measured, body composition will be computed using a noninvasive bioelectric impedance monitor, and hip/waist measurements will be taken. Group A participants will undergo testing at the time of enrolling in the study and after 16 weeks of exercise. Group B participants will undergo these tests after enrollment, after the 16 week waiting period and at the end of the exercise program.

• Participants will also complete two surveys by mail, 3 months and 9 months after completing the exercise portion of the protocol.

Recruitment information / eligibility

• Status: Completed
• Enrollment: 100
• Est. completion date: February 2008
• Est. primary completion date: June 2006
• Accepts healthy volunteers: No
• Gender: Female
• Age group: 18 Years and older

Eligibility

Inclusion Criteria:

• History of pathologically confirmed stage I-IIIa invasive breast cancer

• Adjuvant chemotherapy and/or radiation must be completed at least 3 months prior to enrollment

• Body mass index > 25 and/or a body composition analysis of >30

Exclusion Criteria:

• Patients taking herceptin

• Evidence of residual or distant disease

• Use of any medication expected to affect insulin levels

• Baseline exercise of more than 20 minutes two times per week

• Active malignancy

• Diabetes mellitus

• Heart disease or uncontrolled hypertension

• Presence of any condition that might be expected to impact a participant's ability to perform physical activity

Study Design

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

Related Conditions & MeSH terms

• Breast Cancer
• Breast Neoplasms

Intervention

Behavioral:
• Strength training
One-on-One training with a personal trainer for 50 minutes twice a week using Nautilus machines for 16 weeks.
• Endurance training
Cardiovascular training at home for 30 minutes three times per week for 16 weeks.

Locations

Country	Name	City	State
United States	Dana Farber Cancer Institute	Boston	Massachusetts

Sponsors (1)

Lead Sponsor	Collaborator
Dana-Farber Cancer Institute

Country where clinical trial is conducted

United States, 

References & Publications (2)

Ligibel JA, Campbell N, Partridge A, Chen WY, Salinardi T, Chen H, Adloff K, Keshaviah A, Winer EP. Impact of a mixed strength and endurance exercise intervention on insulin levels in breast cancer survivors. J Clin Oncol. 2008 Feb 20;26(6):907-12. doi: 1 — View Citation

Ligibel JA, Giobbie-Hurder A, Olenczuk D, Campbell N, Salinardi T, Winer EP, Mantzoros CS. Impact of a mixed strength and endurance exercise intervention on levels of adiponectin, high molecular weight adiponectin and leptin in breast cancer survivors. Ca — View Citation

Outcome

Type	Measure	Description	Time frame	Safety issue
Primary	To determine whether strength and endurance training will lower fasting insulin levels in a group of breast cancer survivors.		3 years	No
Secondary	To assess the compliance of a group of breast cancer survivors to a 16 week exercise intervention		3 years	No
Secondary	to determine whether a combination strength and endurance training intervention can increase strength and endurance by 25% over a 16 week training period		3 years	No
Secondary	to evaluate the impact of an exercise intervention on weight, waist-hip ratio and body composition in breast cancer survivors.		3 years	No