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Treatment of Myofascial Trigger Points in common shoulder disorders by physical therapy: a randomised controlled trial

Treatment of Myofascial Trigger Points in common shoulder disorders by physical therapy: a randomised controlled trial

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
ISRCTN
Registry ID
ISRCTN75722066
Enrollment
104
Registered
2007-07-06
Start date
2007-09-01
Completion date
Unknown
Last updated
2021-03-08

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

Conditions

Musculoskeletal chronic shoulder disorders Musculoskeletal Diseases Musculoskeletal chronic shoulder disorders

Interventions

The initial sample size is based on the assumption that the overall score of the primary outcome measure DASH shows a mean improvement of 15 points [SD = 22]. To test the null hypothesis of equality o

Sponsors

Radboud University Nijmegen Medical Centre (The Netherlands)
Lead Sponsor

Eligibility

Inclusion criteria

Inclusion criteria: Between September 2007 and September 2008, all consecutive patients referred to a physical therapy practice specialised in the treatment of individuals with musculoskeletal disorders of the neck, shoulder and arm are potential study participants. The referring physicians include general practioners, orthopaedic surgeons, neurologists and physiatrists. Patients are eligible if they: 1. Have unilateral shoulder complaints (described as pain felt in the shoulder or upper arm) for at least six months 2. Present with persistent shoulder pain that has not spontaneously recovered 3. Are between 18 and 65 years old 4. Because the questionnaires are in the Dutch language, subjects must understand written and verbal Dutch

Exclusion criteria

Exclusion criteria: 1. Diagnosed (prior to the referral) with: 1.1. Shoulder instability 1.2. Shoulder fractures 1.3. Systemic diseases (such as rheumatoid arthritis, Reiter?s syndrome, diabetes) 2. Medical history or examination suggests neurological diseases 3. Other severe medical or psychiatric disorders The project leader will check all the available information from referral letters, additional information from the general practitioner and from the patients.

Design outcomes

Primary

MeasureTime frame
The overall score of the DASH (Disability of Arm Shoulder and Hand) questionnaire - Dutch language version will be used as the primary outcome measure. Timepoints: T0 = baseline T1 = 6 weeks later T2 = 12 weeks later T3 = 26 weeks T4 = 52 weeks

Secondary

MeasureTime frame
1. The total number of shoulder muscles with MTrPs will be counted and compared to the baseline measurement findings 2. Passive range of motion of the shoulder will be measured by an handheld digital inclinometer (The Saunders group Inc, Chaska, MN) 3. The total number of treatment sessions will be counted Timepoints: T0 = baseline T1 = 6 weeks later T2 = 12 weeks later T3 = 26 weeks T4 = 52 weeks

Countries

Netherlands

Outcome results

None listed

Source: ISRCTN (via WHO ICTRP) · Data processed: Apr 6, 2026