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Spots Global Cancer Trial Database for Strength and Range of Motion in Women Undergoing Surgery for Breast Cancer

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We do not endorse or review these studies in any way.

Trial Identification

Brief Title: Strength and Range of Motion in Women Undergoing Surgery for Breast Cancer

Official Title: Breast Clinic Strength and Range of Motion Study

Study ID: NCT00489125

Conditions

Breast Cancer

Interventions

physiologic testing

Study Description

Brief Summary: RATIONALE: Gathering information about strength and range of motion over time from women undergoing surgery for breast cancer may help doctors learn more about recovery from surgery and on-going care. PURPOSE: This clinical trial is collecting information about strength and range of motion over time from women undergoing surgery for breast cancer.

Detailed Description: OBJECTIVES: * Collect data regarding diagnosis, type of surgery, receipt of adjuvant therapy, age, height, weight, waist circumference, arm strength, grip strength, shoulder range of motion, and physical activity participation from women undergoing surgery for breast cancer. * Examine changes in physical activity participation, measures of body composition, shoulder range of motion, grip strength, and arm strength over time in these patients. * Determine differences in changes in physical activity and indices of fitness according to type of surgery and adjuvant therapy. * Examine relationships between exercise participation, fitness, and body composition over time. * Correlate data with an ongoing randomized exercise trial that includes strength and flexibility assessments with no pre-surgery measures. OUTLINE: This is a prospective, cohort study. Patients submit data comprising demographic/medical information, anthropometrics (weight, height, waist circumference), grip strength, bicep strength, shoulder range of motion, and physical activity participation prior to surgery, at each surgical follow-up visit, and at 2 years after surgery.

Eligibility

Minimum Age:

Eligible Ages: CHILD, ADULT, OLDER_ADULT

Sex: FEMALE

Healthy Volunteers: No

Locations

Wake Forest University Comprehensive Cancer Center, Winston-Salem, North Carolina, United States

Contact Details

Name: Shannon Mihalko, PhD

Affiliation: Wake Forest University Health Sciences

Role: PRINCIPAL_INVESTIGATOR

Name: Edward A. Levine, MD

Affiliation: Wake Forest University Health Sciences

Role: PRINCIPAL_INVESTIGATOR

Useful links and downloads for this trial

Clinicaltrials.gov

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