Exercise and Patient Education for Patients With Lateral Hip Pain

Trial statusRecruiting
Trial phaseNot applicable
Trial typeInterventional
Biological sexAll
Age18-75
SponsorJeppe Lange

About this trial

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.

Eligibility criteria

This trial does not accept healthy volunteers

Qualifiers

Age 18-75 years

MRI verified HATP

Lateral hip pain duration > 6 months

Ability to read and understand Danish.

Disqualifiers

Corticosteroid injection in the affected hip joint within the last six weeks prior to the intervention

Previous bone-related surgery to the affected hip,

Signs of bilateral HATP

X-ray verified hip osteoarthritis

Trial design

Design model

Single group

Treatments tested in this trial

  • Exercise and Patient Education

    Procedure/Surgery

    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.

Treatment groups

60 Participants
are divided into 1 treatment group
Group A: Physiotherapist-led exerciseExperimental treatment 1 intervention

Trial outcomes

Primary outcomes

1

Changes in patient-reported pain measured with the revised Copenhagen Hip And Groin Outcome Score (HAGOS) (continuous data)

The subscale "pain" on HAGOS measures the patients perception of hip and/or groin pain. It consist of ten items. A score from 0 to 100 is calculated, where a higher score is indicating lower pain.

Time frame
From baseline to 3 months follow-up. The outcome is also conducted at 6-week follow-up.

Secondary outcomes

1

Changes in patient-reported symptoms measured with the revised Copenhagen Hip And Groin Outcome Score (HAGOS) (continuous data)

The subscale "symptoms" on HAGOS measures the patients perception of hip and/or groin pain. It consist of seven items. A score from 0 to 100 is calculated, where a higher score is indicating lower symptoms.

Time frame
From baseline to 3 months follow-up. The outcome is also conducted at 6-week follow-up.
2

Changes in patient-reported physical function in daily living (ADL) measured with the revised Copenhagen Hip And Groin Outcome Score (HAGOS) (continuous data)

The subscale "ADL" on HAGOS measures the patients perception of hip and/or groin pain. It consist of five items. A score from 0 to 100 is calculated, where a higher score is indicating higher function.

Time frame
From baseline to 3 months follow-up. The outcome is also conducted at 6-week follow-up.
3

Changes in patient-reported physical function in sport and recreational activities (sport/recreation) measured with the revised Copenhagen Hip And Groin Outcome Score (HAGOS) (continuous data)

The subscale "sport/recreation" on HAGOS measures the patients perception of hip and/or groin pain. It consist of eight items. A score from 0 to 100 is calculated, where a higher score is indicating higher function.

Time frame
From baseline to 3 months follow-up. The outcome is also conducted at 6-week follow-up.
4

Changes in patient-reported participation in physical activities (PA) measured with the revised Copenhagen Hip And Groin Outcome Score (HAGOS) (continuous data)

The subscale "PA" on HAGOS measures the patients perception of hip and/or groin pain. It consist of two items. A score from 0 to 100 is calculated, where a higher score is indicating higher ability to participate in physical activity.

Time frame
From baseline to 3 months follow-up. The outcome is also conducted at 6-week follow-up.

Other outcomes

1

Adherence to the exercise program.

The adherence will be calculated as the proportion of completed exercise sessions in relation to the planned exercise sessions. A high adherence will be defined as completion of 75% or more of the planned exercises sessions (both supervised and home-based), medium adherence with completion of 50-74%, and low adherence with completion of less than 50%.

Time frame
From baseline to 3 months follow-up.

Sponsors and contacts

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Jeppe Lange

Lead sponsor

Horsens Hospital

Sponsor institution

University of Aarhus

Collaborator