NCT05687955

Brief Summary

Hip injuries are reported to account for 71% and 29% of all injuries reported in female and male performers, respectively, at the National Institute of Circus Arts. There are no reports on hip pathology in circus performers, nor are there any reported exercise interventions for hip pain in circus performers. This study aims to: To assess the effect of an exercise rehabilitation program on patient-reported outcome measures, hip strength and range of movement, and functional assessments in circus arts students with clinically and radiologically diagnosed hip pain-related disorders. Participants will undertake a 12-week strength exercise protocol that has been specifically designed to focus on hip rehabilitation appropriate for circus performance. Expected outcome: Improvements in patient reported outcome measure (PROM) scores and an increase in function, strength and hip range of movement in people with hip pain

Trial Health

43
At Risk

Trial Health Score

Automated assessment based on enrollment pace, timeline, and geographic reach

Trial has exceeded expected completion date
Enrollment
20

participants targeted

Target at below P25 for not_applicable

Timeline
Completed

Started Mar 2023

Geographic Reach
1 country

1 active site

Status
unknown

Health score is calculated from publicly available data and should be used for screening purposes only.

Trial Relationships

Click on a node to explore related trials.

Study Timeline

Key milestones and dates

First Submitted

Initial submission to the registry

January 4, 2023

Completed
14 days until next milestone

First Posted

Study publicly available on registry

January 18, 2023

Completed
2 months until next milestone

Study Start

First participant enrolled

March 28, 2023

Completed
1 year until next milestone

Primary Completion

Last participant's last visit for primary outcome

March 30, 2024

Completed
Same day until next milestone

Study Completion

Last participant's last visit for all outcomes

March 30, 2024

Completed
Last Updated

May 12, 2023

Status Verified

May 1, 2023

Enrollment Period

1 year

First QC Date

January 4, 2023

Last Update Submit

May 11, 2023

Conditions

Outcome Measures

Primary Outcomes (20)

  • The Copenhagen Hip and Groin Outcome Score (HAGOS)

    Patient Reported Outcome Measure, score on 0-100 scale, with zero representing extreme hip and/or groin problems and 100 representing no hip and/or groin problems.

    Baseline

  • The Copenhagen Hip and Groin Outcome Score (HAGOS)

    Patient Reported Outcome Measure, score on 0-100 scale, with zero representing extreme hip and/or groin problems and 100 representing no hip and/or groin problems.

    3-months

  • The Copenhagen Hip and Groin Outcome Score (HAGOS)

    Patient Reported Outcome Measure, score on 0-100 scale, with zero representing extreme hip and/or groin problems and 100 representing no hip and/or groin problems.

    6-months

  • The Copenhagen Hip and Groin Outcome Score (HAGOS)

    Patient Reported Outcome Measure, score on 0-100 scale, with zero representing extreme hip and/or groin problems and 100 representing no hip and/or groin problems.

    9-months

  • International Hip Outcome Tool (iHOT-12)

    Patient Reported Outcome Measure, scored using a visual analog scale from 0 to 100, with a score of 100 being the best function and least amount of symptoms

    Baseline

  • International Hip Outcome Tool (iHOT-12)

    Patient Reported Outcome Measure scored using a visual analog scale from 0 to 100, with a score of 100 being the best function and least amount of symptoms

    3-months

  • International Hip Outcome Tool (iHOT-12)

    Patient Reported Outcome Measure scored using a visual analog scale from 0 to 100, with a score of 100 being the best function and least amount of symptoms

    6-months

  • International Hip Outcome Tool (iHOT-12)

    Patient Reported Outcome Measure scored using a visual analog scale from 0 to 100, with a score of 100 being the best function and least amount of symptoms

    9-months

  • European Quality of life questionnaire (EQ-5D-5L)

    Patient Reported Outcome Measure

    Baseline

  • European Quality of life questionnaire (EQ-5D-5L)

    Patient Reported Outcome Measure

    3-months

  • European Quality of life questionnaire (EQ-5D-5L)

    Patient Reported Outcome Measure

    6-months

  • European Quality of life questionnaire (EQ-5D-5L)

    Patient Reported Outcome Measure

    9-months

  • Tampa Scale of Kinesiophobia (TSK)

    Patient Reported Outcome Measure

    Baseline

  • Tampa Scale of Kinesiophobia (TSK)

    Patient Reported Outcome Measure

    3-months

  • Tampa Scale of Kinesiophobia (TSK)

    Patient Reported Outcome Measure

    6-months

  • Tampa Scale of Kinesiophobia (TSK)

    Patient Reported Outcome Measure

    9-months

  • Hip Strength assessment

    Strength of hip abduction, adduction, sitting hip flexion at 90deg, prone extension with knee extended, prone external and internal rotation will be measured using a hand-held dynamometer.

    Baseline

  • Hip Strength assessment

    Strength of hip abduction, adduction, sitting hip flexion at 90deg, prone extension with knee extended, prone external and internal rotation will be measured using a hand-held dynamometer.

    9-months

  • Hip Range of Motion

    Hip flexion, Hip internal rotation and external rotation will be measured using an inclinometer

    Baseline

  • Hip Range of Motion

    Hip flexion, Hip internal rotation and external rotation will be measured using an inclinometer

    9-months

Secondary Outcomes (8)

  • Functional movement screen Y-balance test

    Baseline

  • Functional movement screen Y-balance test

    9-months

  • Single leg Hop for distance

    Baseline

  • Single leg Hop for distance

    9-months

  • Trunk Muscle Endurance Test

    Baseline

  • +3 more secondary outcomes

Study Arms (1)

Hip Exercise Program

EXPERIMENTAL

A 12-week strength exercise protocol has been specifically designed to focus on hip rehabilitation appropriate for circus performance.

Other: Hip Exercise Program

Interventions

The exercise intervention is being implemented 3 times per week. Two sessions can be completed at home by the participant, and one session per week will be attended by a physiotherapist that will monitor exercise technique and progress the exercise program for each participant. The exercise protocol has been specifically designed to focus on hip rehabilitation appropriate for circus performance. The exercise program will involve hip strength exercises in the sagittal, coronal and transverse planes using weights and elastic bands (Theraband). It will also include trunk strength and postural correction exercises to address swayback posture which is a common clinical presentation in those with hip dysplasia.

Hip Exercise Program

Eligibility Criteria

Age18 Years - 35 Years
Sexall
Healthy VolunteersNo
Age GroupsAdult (18-64)

You may qualify if:

  • month history hip/groin pain +/- symptoms including clicking, giving way, locking, or catching, one or more of a positive
  • positive FADIR pain provocation test
  • positive HEER test (hip extension and external rotation)
  • positive prone instability test
  • imaging to support a pathological hip (e.g., CAM morphology, hip dysplasia)

You may not qualify if:

  • OA degree \>1 on classification of Tönnis
  • Centre Edge-angle \<10 degrees
  • Legg-Calvé-Perthes or epiphysiolysis
  • history of hip joint surgery or significant hip trauma (fracture +/- dislocation)
  • neurologic motor deficit (lower limb power, strength or reflex deficit)
  • hip pain from a lumbar origin (positive passive straight leg raise, combined lumbar extension and rotation)
  • connective tissue disorder (e.g., Ehlers-danlos or Marfan syndrome)
  • pregnancy or breastfeeding.

Contact the study team to confirm eligibility.

Sponsors & Collaborators

Study Sites (1)

Swinburne University of Technology

Hawthorn, Victoria, 3122, Australia

RECRUITING

MeSH Terms

Conditions

Hip DislocationFemoracetabular Impingement

Condition Hierarchy (Ancestors)

Joint DislocationsJoint DiseasesMusculoskeletal DiseasesWounds and InjuriesHip InjuriesPathologic ProcessesPathological Conditions, Signs and Symptoms

Study Design

Study Type
interventional
Phase
not applicable
Allocation
NA
Masking
NONE
Purpose
TREATMENT
Intervention Model
SINGLE GROUP
Sponsor Type
OTHER
Responsible Party
SPONSOR

Study Record Dates

First Submitted

January 4, 2023

First Posted

January 18, 2023

Study Start

March 28, 2023

Primary Completion

March 30, 2024

Study Completion

March 30, 2024

Last Updated

May 12, 2023

Record last verified: 2023-05

Data Sharing

IPD Sharing
Will not share

Locations