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NCT03954678 · ClinicalTrials.gov registry record · NA
Exercise in Patients Undergoing Urologic Surgery
A NA study of Perioperative Complication, sponsored by Emory University.
- Recruiting
- Registry status
- NA
- Development phase
- 400
- Enrollment target
- 1
- Study location
NCT03954678 is a NA study of Perioperative Complication that is actively recruiting participants, run by Emory University. The registered enrollment target is 400 participants. The trial reports 1 study location across 1 state.
The verdict
NCT03954678, a NA study of Perioperative Complication, is actively recruiting participants, sponsored by Emory University.
- RECRUITING
- Registry status
- NA
- Development phase
- 400 participants
- Enrollment target
- 1
- Study location
Study Summary
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.
Conditions Studied
Interventions
- BEHAVIORAL Exercise Group
- DIETARY_SUPPLEMENT Nutrition Group
Study Locations (1)
Georgia
- Emory University Hospital - Atlanta
Trial Details
| Field | Value |
|---|---|
| Enrollment Target | 400 participants |
| Start Date | 2019-07-30 |
| Est. Completion | 2026-07 |
| Phase | NA |
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Full Details on ClinicalTrials.gov ↗What the Registry Record Tells You About NCT03954678
The ClinicalTrials.gov registry entry for NCT03954678 describes a study currently listed as recruiting, categorized as NA. The registered enrollment target is 400 participants, a figure that helps gauge the scale of data the investigators plan to collect. The listed sponsor is Emory University, which has 1,208 total studies on file at ClinicalTrials.gov.
The record links to 1 condition, with Perioperative Complication appearing as the primary indexed condition, and to 2 interventions - of which Exercise Group is the first listed.
NCT03954678 reports 1 study location spanning 1 distinct geographic area - top geographies include Georgia.
Frequently Asked Questions
What is clinical trial NCT03954678 about?
NCT03954678 is a clinical study titled "Exercise in Patients Undergoing Urologic Surgery". 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 curren...
What is the current status of trial NCT03954678?
This trial is currently recruiting. It is a NA study. The enrollment target is 400 participants. The study started on 2019-07-30. Estimated completion is 2026-07.
What conditions does trial NCT03954678 study?
This clinical trial studies the following conditions: Perioperative Complication.
What interventions are being tested in trial NCT03954678?
The interventions under investigation include: Exercise Group (BEHAVIORAL), Nutrition Group (DIETARY_SUPPLEMENT).
Who is sponsoring clinical trial NCT03954678?
This trial is sponsored by Emory University, which has 1,208 total clinical trials registered on ClinicalTrials.gov.
Where is trial NCT03954678 being conducted?
This trial has 1 study location across Georgia. Contact the study sites directly through ClinicalTrials.gov for enrollment availability.
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