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A Study of Physical Activity in Cancer Survivors

Improving Physical Activity in Rural Cancer Survivors

Status
Completed
Phases
Unknown
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT05988892
Enrollment
100
Registered
2023-08-14
Start date
2023-06-29
Completion date
2025-04-23
Last updated
2026-03-23

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Cancer, Hematopoietic and Lymphatic System Neoplasm, Malignant Solid Neoplasm

Keywords

Rural, Physical Activity

Brief 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.

Interventions

BEHAVIORALPhysical Activity

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.

Sponsors

Mayo Clinic
Lead SponsorOTHER

Study design

Allocation
NA
Intervention model
SINGLE_GROUP
Primary purpose
HEALTH_SERVICES_RESEARCH
Masking
NONE

Eligibility

Sex/Gender
ALL
Age
18 Years to No maximum
Healthy volunteers
Yes

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 Urban Areas 2020 metric) * 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. * Squamous cell or basal cell skin cancers (melanoma still eligible) * Stage 0/in situ vulvar/cervical cancers

Design outcomes

Primary

MeasureTime frameDescription
Change in physical functioning using Short Physical Performance BatteryBaseline; 12 weeksChange in physical functioning based on improvement in endurance, strength, and balance assessed using Short Physical Performance Battery (SPPB) pre- and post-12-week exercise intervention.
Change in Quality of Life (QOL) using Patient-Reported Outcomes Measurement Information System (PROMIS)Baseline; 12 weeksQOL evaluated based on physical functioning and fatigue, assessed using Patient-Reported Outcomes Measurement Information System (PROMIS) pre- and post-12-week exercise intervention.
Change in satisfaction using a 5-point Likert scaleBaseline; 12 weeksSatisfaction assessed using a 5-point Likert scale following 12-week exercise intervention and participant-reporting likelihood of recommending program.
Rate of adherence to program based on participation in virtual exercise sessionsBaseline; 12 weeksAdherence evaluated based on participation in virtual exercise sessions during 12-week exercise intervention.

Countries

United States

Contacts

PRINCIPAL_INVESTIGATORKaye T. Sturz, APRN, CNP

Mayo Clinic Health System in Eau Claire

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Mar 24, 2026