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Trial Title: A Study of Physical Activity in Cancer Survivors

NCT ID: NCT05988892

Condition: Cancer
Hematopoietic and Lymphatic System Neoplasm
Malignant Solid Neoplasm

Conditions: Official terms:
Neoplasms

Conditions: Keywords:
Rural
Physical Activity

Study type: Interventional

Study phase: N/A

Overall status: Recruiting

Study design:

Allocation: N/A

Intervention model: Single Group Assignment

Primary purpose: Health Services Research

Masking: None (Open Label)

Intervention:

Intervention type: Behavioral
Intervention name: Physical Activity
Description: Use Exercise to increase physical activity (PA), as measured by cardiovascular endurance, muscular strength, and balance in underserved cancer survivors >60 years of age and/or those of any age residing at a rural address and to increase quality of life (QOL), as measured by physical functioning and fatigue, in underserved cancer survivors >60 years of age and/or those of any age residing at a rural address.
Arm group label: Community Oncology patients entering cancer survivorship

Summary: The purpose of this study is to determine if increasing physical activity (PA) will increase physical functioning, as measured by cardiovascular endurance, muscular strength, and balance in underserved adult cancer survivors > 60 years of age and/or those of any age residing at a rural address. Also, to determine if increasing PA will increase quality of life (QOL), as measured by physical functioning and fatigue, in underserved cancer survivors >60 years of age and/or those of any age residing at a rural address.

Criteria for eligibility:
Criteria:
Inclusion Criteria: - Adult, cancer survivors (no active disease) at Mayo Clinic Health System (MCHS) in Northwest Wisconsin (NWWI), Southwest Wisconsin (SWWI), Southeast Minnesota (SEMN), or Southwest Minnesota (SWMN) - Any stage cancer - Age ≥18 years residing at a rural address (as defined by Rural America, census.gov) - Completed active treatment of surgery, (neo)adjuvant chemotherapy, and/or (neo) adjuvant radiation. Patients receiving adjuvant endocrine therapy, targeted therapy, or immunotherapy therapies are eligible. - Ownership of a computer/tablet/smartphone with internet access. - Willingness to create a google account and maintain the account for use of the Fitbit - Willingness and ability to attend study visits. - Must be able to complete semi-tandem (10 seconds), side-by-side tandem [10 seconds and short physical performance batters(SPPB)] Score of 6 or greater to qualify for virtual exercise. - Must be ambulatory without the use of assisted device(s). Exclusion Criteria: - Receiving surgery, (neo)adjuvant chemotherapy, (neo) adjuvant radiation, palliative treatment - Are already performing >150 minutes/week of moderate activity or 75 min/week of vigorous physical activity - Cancer-free for greater than 5 years - Unable to complete weekly interventions/exercise due to traveling or unable to be active for more than 7 consecutive days.

Gender: All

Minimum age: 18 Years

Maximum age: N/A

Healthy volunteers: Accepts Healthy Volunteers

Locations:

Facility:
Name: Mayo Clinic Health System-Eau Claire Clinic

Address:
City: Eau Claire
Zip: 54701
Country: United States

Status: Recruiting

Contact:
Last name: Clinical Trials Referral Office

Phone: 855-776-0015
Email: mayocliniccancerstudies@mayo.edu

Contact backup:
Last name: Sara Herrick

Phone: 507-422-9514
Email: Herrick.Sara@mayo.edu

Contact backup:
Last name: Kaye T. Sturz, APRN, CNP

Start date: June 29, 2023

Completion date: December 2025

Lead sponsor:
Agency: Mayo Clinic
Agency class: Other

Source: Mayo Clinic

Record processing date: ClinicalTrials.gov processed this data on November 12, 2024

Source: ClinicalTrials.gov page: https://clinicaltrials.gov/ct2/show/NCT05988892
https://www.mayo.edu/research/clinical-trials

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