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Eccentric Training of the Supraspinatus tendon in Shoulder Impingement syndrome. A pilot study

Eccentric Training of the Supraspinatus tendon in Shoulder Impingement syndrome. A pilot study - Eccentric training in SIS

Status
Active, not recruiting
Phases
Phase 2
Study type
Interventional
Source
NL-OMON
Registry ID
NL-OMON32687
Enrollment
40
Registered
2009-01-09
Start date
2008-07-22
Completion date
Unknown
Last updated
2024-05-06

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Rotator cuff tendinopathy shoulder tendon disease

Interventions

Subjects of the exercise eccentric training program group will perform eccentric home exercises twice a day, 7 days a week, for 12 weeks. The control group will continue their usual care at the phys

Sponsors

Universitair Medisch Centrum Groningen
Lead Sponsor

Eligibility

Age
18 Years to 99 Years

Inclusion criteria

Inclusion criteria: - 1. Painful arc of movement during flexion or abduction* - 2. Positive Neer or Kennedy- Hawkins impingement signs* - 3. Pain on resisted lateral rotation, abduction or Jobe test* - 4. Suffering from SIS with an episode of at least three months and less than one year - 5. Male or female with an age between 18 and 60 years old * Subjects will be included in study if they have at least one positive finding of these categories

Exclusion criteria

Exclusion criteria: . Frozen shoulder - 2. Habitual shoulder luxation in the previous 2 years - 3. (History of) shoulder fracture - 4. Previous shoulder surgery - 5. Cervical radiculopathy - 6. Inflammatory rheumatic diseases - 7. Other musculoskeletal problems of an upper limb - 8. Bilateral SIS - 9. Unable to complete (Dutch) questionnaires

Design outcomes

Secondary

MeasureTime frame
The following secondary outcomes will be used: - Constant -score, to assess shoulder function - 2. Shoulder pain questionnaire, to assess the amount of shoulder pain - 3. Compliance - 4. Illness perception - 5. Satisfaction At the intake (T0), after 6 (T1) and after 12 weeks (T2) the shoulder function will be assessed with questionnaires and shoulder function tests. Outcomes of both groups (eccentric strengthening training and usual care) will be compared to assess the effect of the eccentric strengthening training program.

Primary

MeasureTime frame
Main outcome of the study is rcovery, assessed with the Shoulder Disability Questionnaire.

Countries

Netherlands

Outcome results

None listed

Source: NL-OMON (via WHO ICTRP)