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Endometrial Cancer Diet and Exercise

Physical Activity and Nutrition Counseling Intervention in Endometrial Cancer Survivors

Status
Completed
Phases
NA
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT02987881
Enrollment
16
Registered
2016-12-09
Start date
2017-02-01
Completion date
2019-06-01
Last updated
2021-08-02

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

Conditions

Early Stage Endometrial Cancer

Brief summary

This study will evaluate whether the use of the Jawbone wristband monitor, in connection with home-based exercise and nutritional counseling can be safely completed and improve cardiorespiratory fitness (heart and lung health) in women with early stage endometrial cancer who have undergone surgery.

Interventions

BEHAVIORALHome-based aerobic exercise and nutritional counseling

Moderate walking and running with nutritional counseling at study visits.

Sponsors

Duke Cancer Institute
CollaboratorOTHER
Duke University
Lead SponsorOTHER

Study design

Allocation
NA
Intervention model
SINGLE_GROUP
Primary purpose
SUPPORTIVE_CARE
Masking
NONE

Masking description

Open Label

Eligibility

Sex/Gender
FEMALE
Age
18 Years to No maximum
Healthy volunteers
No

Inclusion criteria

* Ages \> 18 years. * Localized endometrial cancer (stage I and II); no evidence of stage III or IV disease. * At least 2 months was passed since the hysterectomy and enrollment. * Karnofsky performance status \> 70%. * Body mass index of 30.0 - 49.9 and body weight \< 300 pounds. * No plan for adjuvant endometrial cancer therapy. * Able to exercise safely on a treadmill. * No absolute contraindications to exercise testing as recommended by the American Thoracic Society. No recent (\<6 months) acute cardiac event unstable angina, uncontrolled dysrhythmias causing symptoms or hemodynamic compromise, symptomatic aortic stenosis, uncontrolled symptomatic heart failure, acute pulmonary embolus, acute myocarditis or pericarditis, suspected or known dissecting aneurism and acute systemic infection. * The subject is not participating in regular physical exercise (more than 60 minutes of moderate intensity or 30 minutes of vigorous intensity exercise per week) or weight reduction dieting. * Able to provide informed consent. * Have reliable transportation to the testing facilities. * Subjects must be able to speak and understand English to participate in this study. * Subjects must have a personal mobile device compatible for the activity monitor Compatible devices for the activity monitors are below: * Android o Activity monitor is compatible with most Android devices equipped with Bluetooth 4.0 and running Android 4.3 (Jelly Bean) or later. * iOS * iPhone 4s (or newer) * iPod touch (5th generation or newer) * iPad (3rd generation or newer) * iPad mini (1st generation or newer) * iPad Air (1st generation or newer)

Exclusion criteria

\-

Design outcomes

Primary

MeasureTime frameDescription
change in cardiorespiratory fitness and CVD risk profile as measured by body compositionbaseline and 12 weeks
Feasibility as measured by adherence to weekly walking sessionsWeek 12Percentage of daily steps divided by total number of steps and daily walking sessions divided by total number of sessions prescribed
Safety as measured by the type and prevalence of adverse events during study-related assessmentsWeek 12Collection of events related to cardiopulmonary testing and self-reported events during off-site exercise training
change in cardiorespiratory fitness and CVD risk profile as measured by VO2peakbaseline and 12 weeks
change in cardiorespiratory fitness and CVD risk profile as measured by blood pressurebaseline and 12 weeks
change in cardiorespiratory fitness and CVD risk profile as measured by lipid profilebaseline and 12 weeks
change in cardiorespiratory fitness and CVD risk profile as measured by C-reactive proteinbaseline and 12 weeks

Secondary

MeasureTime frame
patient experience with exercise and nutrition counseling as measured by telephone questionnaire16 weeks

Countries

United States

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 4, 2026