Exercise for Subacromial Pain Syndrome

NCT ID: NCT03317808

Last Updated: 2019-01-25

Study Results

Results pending

The study team has not published outcome measurements, participant flow, or safety data for this trial yet. Check back later for updates.

Basic Information

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Recruitment Status

COMPLETED

Clinical Phase

NA

Total Enrollment

22 participants

Study Classification

INTERVENTIONAL

Study Start Date

2017-10-16

Study Completion Date

2018-12-13

Brief Summary

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This study evaluates the effect of Heavy Slow Resistance exercise (HSR) exercise in comparison with traditional supervised exercise as treatment for patients with subacromial shoulder pain. The purpose is to evaluate if HSR is feasible fir these patients, and compare its effect to traditional exercise at pain and function of the shoulder. One half will complete the heavy slow resistance exercise, the other will complete the conventional exercise.

Detailed Description

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Conditions

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Subacromial Pain Syndrome

Study Design

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Allocation Method

RANDOMIZED

Intervention Model

PARALLEL

Primary Study Purpose

TREATMENT

Blinding Strategy

DOUBLE

Investigators Outcome Assessors

Study Groups

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Heavy slow resistance exercise

Group Type ACTIVE_COMPARATOR

Different exercise

Intervention Type DIAGNOSTIC_TEST

Evaluating the difference between Heavy slow resistance and traditional exercise, based on the SPADI score.

Traditional supervised exercise

Group Type PLACEBO_COMPARATOR

Different exercise

Intervention Type DIAGNOSTIC_TEST

Evaluating the difference between Heavy slow resistance and traditional exercise, based on the SPADI score.

Interventions

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Different exercise

Evaluating the difference between Heavy slow resistance and traditional exercise, based on the SPADI score.

Intervention Type DIAGNOSTIC_TEST

Eligibility Criteria

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Inclusion Criteria

* Shoulder pain \> Three months
* Subacromial pain
* Dysfunction or pain during abduction
* Pain during isometric strength test of abduction or external rotation of the shoulder.
* Positive Hawkins test
* Normal passive range of movement in the glenohumeral joint

Exclusion Criteria

* Surgery of the affected shoulder
* Patients that are not considered suitable to complete the treatment, or able to answer a Norwegian questionnaire
* Shoulder dislocation or shoulder instability
* Clinical sign of cervical nerve root affection
* Rheumatoid arthritis
* Clinical sign of full rupture of the rotator cuff.
* Pregnancy
* Cortisone injection past six weeks
Minimum Eligible Age

25 Years

Maximum Eligible Age

70 Years

Eligible Sex

ALL

Accepts Healthy Volunteers

No

Sponsors

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Oslo University Hospital

OTHER

Sponsor Role lead

Responsible Party

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Hans-Hugo Fredriksen Høiland

Stud.med

Responsibility Role PRINCIPAL_INVESTIGATOR

Principal Investigators

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Høiland

Role: PRINCIPAL_INVESTIGATOR

Oslo University Hospital

Locations

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Ullevål Sykehus

Oslo, , Norway

Site Status

Countries

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Norway

Other Identifiers

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2017/1277

Identifier Type: -

Identifier Source: org_study_id

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