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NCT06525701 · ClinicalTrials.gov registry record · NA

Surgeon Core-strengthening Program as a Modifier for Exertion Associated With Vaginal Surgery

A NA study of Musculoskeletal Pain and Musculoskeletal Injury, sponsored by Loyola University.

Completed
Registry status
NA
Development phase
18
Enrollment target
1
Study location

NCT06525701: Completed NA study of Musculoskeletal Pain and Musculoskeletal Injury, sponsored by Loyola University.

NCT06525701 is a NA study of Musculoskeletal Pain and Musculoskeletal Injury that has completed, run by Loyola University. The registered enrollment target is 18 participants, below the 155-participant average among 37 other Musculoskeletal Pain trials with a reported enrollment target (88% lower). The trial reports 1 study location across 1 state. According to ClinicalTrials.gov, the official US trial registry.

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The verdict

NCT06525701, a NA study of Musculoskeletal Pain and Musculoskeletal Injury, has completed, sponsored by Loyola University.

COMPLETED
Registry status
NA
Development phase
18 participants
Enrollment target
1
Study location

Study Summary

Work-related musculoskeletal pain and injury is a growing concern in surgery. Vaginal surgery has unique ergonomic risks, but no studies have addressed the potential for an exercise regimen to reduce physical strain by vaginal surgeons

Primary Outcome

The effect of a core-strengthening program on surgeons' physical exertion during and after vaginal prolapse surgery as measured by the Borg Category Ratio (CR-10). The Borg Category Ratio scale is a self-reported tool that describes level of exertion and ranges from 0-10 where larger numbers represent greater exertion.

Interventions

  • OTHER Control Group
  • OTHER Execise Group

Study Locations (1)

Illinois

  • Loyola University Medical Center - Maywood

Trial Details

FieldValue
Enrollment Target 18 participants
Start Date 2024-08-12
Est. Completion 2025-07-01
Phase NA
Loyola University

92 total trials

What the finished NCT06525701 record still lists

NCT06525701 is an interventional study that assigns participants to a tested intervention. The registry caps enrollment at 18 participants, a relatively small participant target, below the 155-participant average among 37 other Musculoskeletal Pain trials with a reported enrollment target (88% lower).

The record links to 2 conditions, with Musculoskeletal Pain appearing as the primary indexed condition, and to 2 interventions - of which Control Group is the first listed.

NCT06525701 reports a single indexed study location in Illinois.

Frequently Asked Questions

What is clinical trial NCT06525701 about?

NCT06525701 is a clinical study titled "Surgeon Core-strengthening Program as a Modifier for Exertion Associated With Vaginal Surgery". Work-related musculoskeletal pain and injury is a growing concern in surgery. Vaginal surgery has unique ergonomic risks, but no studies have addressed the potential for an exercise regimen to reduce physical strain by vaginal surgeons

What is the current status of trial NCT06525701?

This trial is currently completed. It is a NA study. The enrollment target is 18 participants. The study started on 2024-08-12. Estimated completion is 2025-07-01.

What conditions does trial NCT06525701 study?

This clinical trial studies the following conditions: Musculoskeletal Pain, Musculoskeletal Injury.

What interventions are being tested in trial NCT06525701?

The interventions under investigation include: Control Group (OTHER), Execise Group (OTHER).

Who is sponsoring clinical trial NCT06525701?

This trial is sponsored by Loyola University, which has 92 total clinical trials registered on ClinicalTrials.gov.

Where is trial NCT06525701 being conducted?

This trial has 1 study location across Illinois. Contact the study sites directly through ClinicalTrials.gov for enrollment availability.

Similar trials for Musculoskeletal Pain

Matched on the same primary condition, ranked to surface studies in the same phase first, then by recruiting status, no relevance scoring or editorial curation.

Where NCT06525701's enrollment target sits among peer trials

18 34th of 37 higher than 4 of 37 other Musculoskeletal Pain trials

participants (enrollment target), bucketed by value

Each bar is a band; taller bars hold more other Musculoskeletal Pain trials. The dashed line + filled bar mark this entry. Hover or tap any bar for its full count and share, and where it sits relative to this entry.

Source ClinicalTrials.gov registry export · 2026-08-08

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Source: ClinicalTrials.gov NCT06525701, the US trial registry maintained by the National Library of Medicine. NCT06525701 (small enrollment · single site footprint · completed) retrieved and formatted by PlainTrial, see methodology.