Activity and Cancer Survivorship Exercise Pilot

N/AActive Not RecruitingNCT07283029

University of Iowa10 enrolled

Overview

This early phase I clinical trial measures the changes in functional fitness following home-based comprehensive exercise program in patients who have endometrial cancer who have completed treatment. Endometrial cancer is an increasingly common diagnosis, with health and quality of life concerns persisting after the active cancer treatment period. Exercise in cancer survivors has the potential to reduce the risk of death by improving cardiovascular fitness, quality of life, strength, longevity, and independence. A home-based exercise programs may be a feasible approach for exercise programming in patients who have endometrial cancer who have completed treatment.

Study Type

INTERVENTIONAL

Allocation

Purpose

SUPPORTIVE_CARE

Masking

NONE

Enrollment

Conditions

Endometrial Cancer

Interventions

Eligibility

Sex: FEMALEMin age: 18 YearsMax age: 74 Years

Medical Language ↔ Plain English

Inclusion Criteria: * Willing to provide written informed consent * Willing to comply with all study procedures and be available for the duration of the study * Fluent in spoken and written English * Women 18-74 years of age * Documented diagnosis of type I, stage I-IIIc endometrial cancer within the past 5 years * Completion of current treatment for endometrial cancer * Technology access (cellphone with data, broadband internet, WiFi) for tele coaching * Pass the Physical Activity Readiness Questionnaire (PAR-Q) Exclusion Criteria: * Absolute contraindications to exercise (i.e., acute myocardial infarction, severe orthopedic or musculoskeletal limitations * Have evidence of recurrent or metastatic disease * Are currently performing resistance training \>= 2 days per week * Are currently exceeding 150 minutes of at least moderate intensity activity per week * Report of chest pain, shortness of breath, fainting, or angina pectoris * Have physical disability that would limit range of motion through exercises such as sitting, standing and inability to walk one block * Plans to move from the area * Enrolled in another clinical trial or has used of any investigational drugs, biologics, or devices within 30 days prior to randomization * Women who are pregnant or breast-feeding * Not suitable for study participation due to other reasons at the discretion of the investigator * Failing the Physical Activity Readiness Questionnaire

Outcomes

Primary Outcomes

Chair sit to stand test

Will be assessed using the Functional Fitness Test, which is a battery of six tests including the 30 second chair stand, the 30 second arm curl, the 6-minute walk, the chair sit and reach, the 8-foot up and go, and the back scratch tests. Mixed effects regression models will be used to estimate changes in each of the 6 tests included in the Functional Fitness Test from pre- to post-intervention. Random effects will be included to account for the longitudinally correlated nature of repeat measurements within a patient. Estimated mean changes and associated 90% confidence intervals will be reported. Primary outcome is number of repetitions in the chair sit to stand test

Time frame: baseline, pre-intervention and immediately after the intervention

Secondary Outcomes

Incidence of adverse events

Will be summarized by system organ class and/or preferred term, type of adverse event, severity (based on National Cancer Institute Common Terminology Criteria for Adverse Events (CTCAE) version 5.0, \[NCI CTCAE v 5.0\] grades), and relation to study treatment. The most severe grade per patient will be reported.

Time frame: Up to 10 weeks

Muscle strengthening exercise session adherence

Exercise session adherence will be defined as the proportion of planned exercise sessions in which a participant completes at least 50% of the prescribed exercises. The mean and associated 90% confidence interval will be reported

Time frame: Up to 10 weeks

Aerobic physical activity adherence

Aerobic physical activity adherence will be defined as the proportion of planned weeks a participant accumulates 150 minutes of moderate intensity activity. The mean and associated 90% confidence interval will be reported.

Time frame: Up to 10 weeks

Tele coaching adherence

Tele coaching adherence will be defined as the proportion of planned exercise sessions in which a participant completes. The mean and associated 90% confidence interval will be reported.

Time frame: Up to 10 weeks

Exercise program acceptability

Acceptability will be assessed using Likert scale ratings of quality of exercise equipment, educational materials, health coaching, study feedback and distance-delivery format. Means and associated 90% confidence intervals will be reported for each item.

Time frame: Up to 10 weeks

Body weight

Will be assessed by the within patient change of weight, waist and hip circumferences will be assessed from pre- to post-intervention. Mixed effects regression models will be used to estimate changes in anthropometrics. Random effects will be included to account for the longitudinally correlated nature of repeat measurements within a patient. Estimated mean changes and associated 90% confidence intervals will be reported. Primary secondary outcome is changes in weight.

Time frame: baseline, pre-intervention and immediately after the intervention

Ambulatory activity levels

Will be assessed by the within patient change in average daily steps taken within a week will be assessed from pre- to post-intervention. Mixed effects regression models will be used to estimate changes in ambulatory activity levels. Random effects will be included to account for the longitudinally correlated nature of repeat measurements within a patient. Estimated mean and associated 90% confidence interval will be reported.

Time frame: baseline, pre-intervention and immediately after the intervention

Activity and Cancer Survivorship Exercise Pilot

Overview

Conditions

Interventions

Eligibility

Locations (1)

Outcomes

Primary Outcomes

Secondary Outcomes