RECRUITING

Exercise in Patients Undergoing Urologic Surgery

Study Overview

This clinical trial focuses on testing the efficacy of different digital interventions to promote re-engagement in cancer-related long-term follow-up care for adolescent and young adult (AYA) survivors of childhood cancer.

Description

Patients who are being scheduled for an operative procedure with an inpatient postoperative stay are eligible for this study. Participants will be selected to start a physical fitness plan or a nutrition plan at the time of surgical scheduling. Each participant will be asked to continue their current lifestyle for two days after their pre-operative appointment to get a baseline of activity (by pedometer and functional tests) and nutritional risk (by questionnaire). After two days, patients in the activity group will start their activity plans. They will be encouraged to get 10,000 steps per day and to perform whole body strength training exercises 3 times a week. Five days before and after surgery, participants in the nutrition group will be asked to consume a standard liquid nutrition supplement (i.e. Boost or Ensure) two times per day. Participants in the activity group will record steps and number of strength training sessions completed, while patients in the nutrition group will record the number of supplements consumed.

Official Title

Prospective Randomized Study of Exercise in Patients Undergoing Urologic Surgery

Quick Facts

Study Start:2019-07-30
Study Completion:2025-06
Study Type:Not specified
Phase:Not Applicable
Enrollment:Not specified
Status:RECRUITING

Study ID

NCT03954678

Participation Criteria

Researchers look for people who fit a certain description, called eligibility criteria. Some examples of these criteria are a person's general health condition or prior treatments.

Ages Eligible for Study:18 Years
Sexes Eligible for Study:ALL
Accepts Healthy Volunteers:No
Standard Ages:ADULT, OLDER_ADULT
Inclusion CriteriaExclusion Criteria
  1. * Patients scheduled for operative procedure with an inpatient postoperative stay are eligible for this study
  2. * Patients willing and able to give blood sample as part of standard of care labs
  3. * Patients willing and able to fill out questionnaire
  4. * Patients who will fill out the step log daily
  5. * Patients willing and able to sign informed consent
  1. * None

Contacts and Locations

Study Contact

Kenneth Ogan, MD
CONTACT
(404) 778-4898
kogan@emory.edu

Principal Investigator

Kenneth Ogan, MD
PRINCIPAL_INVESTIGATOR
Emory University

Study Locations (Sites)

Emory University Hospital
Atlanta, Georgia, 30322
United States

Collaborators and Investigators

Sponsor: Emory University

  • Kenneth Ogan, MD, PRINCIPAL_INVESTIGATOR, Emory University

Study Record Dates

These dates track the progress of study record and summary results submissions to ClinicalTrials.gov. Study records and reported results are reviewed by the National Library of Medicine (NLM) to make sure they meet specific quality control standards before being posted on the public website.

Study Registration Dates

Study Start Date2019-07-30
Study Completion Date2025-06

Study Record Updates

Study Start Date2019-07-30
Study Completion Date2025-06

Terms related to this study

Keywords Provided by Researchers

  • Exercise
  • Nutrition supplement
  • Surgery

Additional Relevant MeSH Terms

  • Perioperative Complication