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Clinical Trials/NCT02529150
NCT02529150
Completed
Not Applicable

WISER After Ovarian Cancer - Exercise Pilot Study

Abramson Cancer Center at Penn Medicine1 site in 1 country10 target enrollmentMay 2015
ConditionsOvarian Cancer

Overview

Phase
Not Applicable
Intervention
Not specified
Conditions
Ovarian Cancer
Sponsor
Abramson Cancer Center at Penn Medicine
Enrollment
10
Locations
1
Primary Endpoint
Number of adverse events
Status
Completed
Last Updated
6 years ago

Overview

Brief Summary

One in four deaths in the United States is due to cancer, and one in three women will develop cancer in her lifetime. Despite improvements in survival among other forms of cancer, ovarian cancer prognosis remains poor. Eighty percent of women with ovarian cancer will present with advanced disease (stage 3 or 4) where 5-year survival ranges from 18-34%.2 Among patients with stage III and IV epithelial ovarian cancer (EOC), recurrence rates are high.4 Therefore, interventions focused on preventing recurrence or slowing progression of EOC is a critical problem in the field. The investigators have submitted an R21 to NCI for a dose response exercise intervention trial to examine the dose response effects of aerobic exercise on biomarkers relevant to ovarian cancer progression and recurrence. The reviewers would like assurance that the investigators can recruit ovarian cancer patients into an exercise study and that these women will do the exercise protocol we plan to prescribe in our high dose of exercise.

Registry
clinicaltrials.gov
Start Date
May 2015
End Date
May 6, 2016
Last Updated
6 years ago
Study Type
Interventional
Study Design
Single Group
Sex
Female

Investigators

Responsible Party
Sponsor

Eligibility Criteria

Inclusion Criteria

  • Diagnosis of stage III-IV EOC, completed surgery,
  • \> 12 months life expectancy (physician estimate),
  • able to walk 15 minutes at a time (use of a cane is acceptable).

Exclusion Criteria

  • medical or psychiatric conditions (beyond ovarian cancer, its treatment, and its symptoms) that would impair our ability to test study hypotheses (e.g. cardiac, pulmonary, or
  • orthopedic history that would prohibit a program of walking for exercise;
  • psychotic disorders,
  • dementia,
  • inability to give informed consent

Outcomes

Primary Outcomes

Number of adverse events

Time Frame: 26 weeks

Study Sites (1)

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