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Prospective randomised pilotstudy physiotherapy for patients with a subacromial-impingementsyndrome

Prospective randomised pilotstudy physiotherapy for patients with a subacromial-impingementsyndrome - Pilotstudy physiotherapy for shouldercomplaints

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
NL-OMON
Registry ID
NL-OMON31726
Enrollment
20
Registered
2008-05-07
Start date
2008-06-16
Completion date
Unknown
Last updated
2024-05-13

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

Conditions

CANS (complaints of the arm neck and/or shoulder)

Interventions

During a period of three months patients will receive six sessions of treatment with tape or manual therapy in wide sense. Both methods of treatment will be given by a manual therapist.

Sponsors

Medisch Centrum Alkmaar
Lead Sponsor

Eligibility

Age
18 Years to 99 Years

Inclusion criteria

Inclusion criteria: Positive impingement tests and significant reduction of pain for the same tests after an injection of 8 ml 1% lidocaïne in the subacromial area, Duration of shouderpain between 1/2 and 2 years, Age between 35 and 70 years, Patients accept the consequences of participation at the study

Exclusion criteria

Exclusion criteria: Anatomical abnormalities as dysplasie art. glenohumeralis, total cufftear etc. confirmed with radiography and/or sonography (with exception of minor arthrosis, calcifications and partial cufftears), Being operated at the shoulder or cervical spine, Reumatic diseases as polymyalgia rheumatica, artritis rheumatica, lupus erythematosis en fibromyalgia, Severe arthritis of the glenohumeral joint, The shoulder has been treated by three or more injections with cortisone, Professional sportactivities with severe stress on the shoulder (hockey, golf, javelin throwing), Severe disease or suspected of a severe disease (as malignities), Complaints in both shoulders, Severe trauma of the shoulder last 6 months, Neurologic disease with negative consequences for the shoulder (as CVA, MS, Parkinson), Diabetis mellitis with the dependence of insuline, Luxation or fracture of the shoulder in the past, Cervico-radicular syndrome, Pathology of organs with negative consequences for the shoulder, Demented, Psychiatric diseases, Insufficient understanding of the Dutch language, Very bad general condition, Very bad condition of the skin because of a skindisease, Allergic for tape.

Design outcomes

Primary

MeasureTime frame
- Perceived overall improvement compared to baseline on a 7 point Likertscale. - Severity of perceived disability by means of the 'Disabilities of the Arm, Shoulder and Hand Scale' (DASH).

Secondary

MeasureTime frame
- Pain (VAS) - Individual disability measure - Mobility of the shoulder - 'Constant-Murley' score (a combination of pain, activities in daily life, mobility and strength) - Quality of life (Rand 36) - Cost-effectiveness (Health related quality of life and economic consequences will be assessed, the latter by means of a cost-diary. Costs of allocated treatment, direct and non-direct health care costs, and direct non-health care costs will be determined.)

Countries

Netherlands

Outcome results

None listed

Source: NL-OMON (via WHO ICTRP)