- ICH GCP
- US Clinical Trials Registry
- Clinical Trial NCT01236417
Exercise Intervention in Breast Cancer Patients With Treatment-Induced Arthralgia
April 12, 2012 updated by: Roswell Park Cancer Institute
This is a pilot study of a specifically designed exercise intervention developed for breast cancer patients with aromatase-inhibitor related joint pain.
Study Overview
Status
Completed
Conditions
Intervention / Treatment
Study Type
Interventional
Enrollment (Actual)
27
Phase
- Not Applicable
Contacts and Locations
This section provides the contact details for those conducting the study, and information on where this study is being conducted.
Study Locations
-
-
New York
-
Buffalo, New York, United States, 14263
- Roswell Park Cancer Institute
-
-
Participation Criteria
Researchers look for people who fit a certain description, called eligibility criteria. Some examples of these criteria are a person's general health condition or prior treatments.
Eligibility Criteria
Ages Eligible for Study
18 years and older (Adult, Older Adult)
Accepts Healthy Volunteers
No
Genders Eligible for Study
Female
Description
Inclusion Criteria:
- Post menopausal women with a history of estrogen positive breast cancer who are receiving aromatase inhibitors for at least one month.
- Patients must complain of mild to moderate arthralgia.
- Ability to understand and sign informed consent.
- Patients meet criteria for low to moderate risk for moderate exercise based oon the ACSM guidelines.
Exclusion Criteria:
- Inability to comply with study requirements.
- Metastatic breast cancer.
- Patients with orthopedic or neuromuscular disorders that preclude participation in exercise.
- Rheumatoid arthritis.
- History of MI, angina or congestive heart failure.
- Pregnant or lactating females.
- Patients that are high risk for moderate exercise based on ACSM risk classification.
- Patients who exceed minimal physical activity recommendations from the US Surgeon General's Report: Accumulation of 30 minutes or more of moderate physical activity on most days of the week.
- Morbidly obese with BMI ≥ 40
Study Plan
This section provides details of the study plan, including how the study is designed and what the study is measuring.
How is the study designed?
Design Details
- Primary Purpose: Prevention
- Allocation: N/A
- Interventional Model: Single Group Assignment
- Masking: None (Open Label)
Arms and Interventions
Participant Group / Arm |
Intervention / Treatment |
---|---|
Experimental: Exercise
Subjects will be participating in a home-based flexibility and exercise program
|
Exercising for 8 weeks using an elastic band
|
What is the study measuring?
Primary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
---|---|---|
Effects of exercise
Time Frame: Length of study
|
To assess the effect of an exercise intervention in breast cancer patients with arthralgia secondary to adjuvant treatment with aromatase inhibitors.
|
Length of study
|
Secondary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
---|---|---|
Feasibility of Multi-institutional study
Time Frame: Length of the study
|
To perform a pilot to access the feasibility of a multi-institutional approach
|
Length of the study
|
Collaborators and Investigators
This is where you will find people and organizations involved with this study.
Sponsor
Investigators
- Principal Investigator: Tracy O'Connor, MD, Roswell Park Cancer Institute
Study record dates
These dates track the progress of study record and summary results submissions to ClinicalTrials.gov. Study records and reported results are reviewed by the National Library of Medicine (NLM) to make sure they meet specific quality control standards before being posted on the public website.
Study Major Dates
Study Start
March 1, 2010
Primary Completion (Actual)
March 1, 2012
Study Registration Dates
First Submitted
November 5, 2010
First Submitted That Met QC Criteria
November 5, 2010
First Posted (Estimate)
November 7, 2010
Study Record Updates
Last Update Posted (Estimate)
April 13, 2012
Last Update Submitted That Met QC Criteria
April 12, 2012
Last Verified
April 1, 2012
More Information
Terms related to this study
Additional Relevant MeSH Terms
Other Study ID Numbers
- I 169310
This information was retrieved directly from the website clinicaltrials.gov without any changes. If you have any requests to change, remove or update your study details, please contact register@clinicaltrials.gov. As soon as a change is implemented on clinicaltrials.gov, this will be updated automatically on our website as well.
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