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Randomized controlled trial of taping patients with a shoulder subacromial impingement syndrome

Randomized controlled trial of taping patients with a shoulder subacromial impingement syndrome - physiotherapy for shouldercomplaints

Status
Active, not recruiting
Phases
Phase 2
Study type
Interventional
Source
NL-OMON
Registry ID
NL-OMON35014
Enrollment
140
Registered
2010-09-20
Start date
2010-09-08
Completion date
Unknown
Last updated
2025-03-24

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

Conditions

shoulder complaints subacromial impingement syndrome

Interventions

1. Usual care: Physiotherapy or manual therapy 2. Usual care plus taping Physiotherapy or manual therapy At the end of each treatment session the schouder of the patient will be strapped. The tape d

Sponsors

Academisch Medisch Centrum
Lead Sponsor

Eligibility

Age
18 Years to 99 Years

Inclusion criteria

Inclusion criteria: signs of subacromial impingement complaints with history taking at least two positive impingementtests age between 18 and 65 years willing to participate

Exclusion criteria

Exclusion criteria: severe radiculopathy serious co-morbidity serious psychopathology previous surgery of the shoulder major shouldertrauma in teh previous 6 months severe synovitis of the glenohumeral joint not able to speak and understand Dutch

Design outcomes

Primary

MeasureTime frame
- Pain intensity will be measured on an 11-point numerical rating scale (0=no pain to 10=worst imaginable pain). - Functional status will be measured according to the Dutch version of 'Disabilities of the Arm, Shoulder and Hand Scale' (DASH). The DASH is widely used in shoulder pain studies, and has shown a good content and construct validity, and a good reliability and responsiveness.

Secondary

MeasureTime frame
- De main complaint of the patient will be recorded and scored on a visual analoque scale (0=no restriction, 10=not possible) - Global perceived recovery will be measured by self-assessment on a 7-point Likert scale ranging from *completely recovered* to *worse than ever* - The reasons for prematurely terminating treatment will be recorded.

Countries

Netherlands

Outcome results

None listed

Source: NL-OMON (via WHO ICTRP)