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Exercise and Patient Education for Patients With Lateral Hip Pain

NCT06418217 · Status: RECRUITING · Phase: NA · Type: INTERVENTIONAL · Enrollment: 60

Last updated 2025-06-26

No results posted yet for this study

Summary

This prospective cohort trial will investigate a progressive exercise protocol and patient education for patients with hip abductor tendon pathology. The primary outcome is patient reported pain measured by the revised Copenhagen Hip And Groin Outcome Score (HAGOS), that will be conducted at baseline and at a 12 week follow-up.

Conditions

  • Gluteal Tendinitis
  • Greater Trochanteric Pain Syndrome
  • Hip and Thigh Injury
  • Rupture of Hip Abductor Tendon (Disorder)

Interventions

PROCEDURE

Exercise and Patient Education

Patients will undergo a 12-week physiotherapist-led exercise program consisting of 8 supervised sessions and home-based training in between. Patients will keep training diaries, where each session is tracked in regards of completed repetitions and pain before and after the sessions. Each session will consist of four exercises.

Sponsors & Collaborators

  • University of Aarhus

    collaborator OTHER

  • Jeppe Lange

    lead OTHER

Principal Investigators

  • Mathias Høgsholt, PT, PhD.st. · Horsens Regional Hospital; Aarhus University

  • Jeppe Lange, MD, PhD · Horsens Regional Hospital; Aarhus University

  • Signe Kierkegaard-Brøchner, PhD · Regionshospitalet Horsens

  • Kristian Thorborg, PhD · Copenhagen University Hospital, Hvidovre

  • Marie Bagger Bohn, MD, PhD · Regionshospitalet Horsens

Study Design

Allocation
NA
Purpose
TREATMENT
Masking
NONE
Model
SINGLE_GROUP

Eligibility

Min Age
18 Years
Max Age
75 Years
Sex
ALL
Healthy Volunteers
No

Timeline & Regulatory

Start
2024-05-17
Primary Completion
2026-11-01
Completion
2027-02-01

Countries

  • Denmark

Study Locations

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Read the full study record

This page highlights key information. For complete eligibility criteria, study locations, investigator contacts, and the full protocol, visit the original record on ClinicalTrials.gov.

View NCT06418217 on ClinicalTrials.gov