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An investigation of the reliability of the Shoulder Symptom Modification Procedure in people with shoulder pain

An investigation of the reliability of the Shoulder Symptom Modification Procedure in people with shoulder pain: an observational cross-sectional study

Status
Active, not recruiting
Phases
Unknown
Study type
Observational
Source
ISRCTN
Registry ID
ISRCTN95412360
Enrollment
12
Registered
2016-04-22
Start date
2016-04-21
Completion date
Unknown
Last updated
2017-08-21

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

Conditions

Shoulder pain of musculoskeletal origin Musculoskeletal Diseases

Interventions

The study involves taking videos of people with shoulder pain undergoing a clinical examination, followed by viewing and scoring of this clinical examination by a number of physiotherapists, in order

Sponsors

University of Limerick
Lead Sponsor

Eligibility

Sex/Gender
All

Inclusion criteria

Inclusion criteria: Shoulder pain participants: Inclusion criteria: over 18 years, shoulder pain is reproduced by one or more shoulder movements, provision of informed written consent. Physiotherapists: A group of up to 30 registered qualified physiotherapists will act as the raters

Exclusion criteria

Exclusion criteria: 1. People who have recent shoulder surgery or fracture 2. People with rheumatological or neurological cause for shoulder pain, or potentially serious conditions e.g. systemic disease, neurological disorders, inflammatory conditions or major trauma 3. People who have had physiotherapy treatment resulting in resolution of their pain

Design outcomes

Primary

MeasureTime frame
Reliability of physiotherapist participants to determine the effect of a series of procedures (that comprise the Shoulder Symptom Modification Procedure) on the patient participant’s shoulder symptoms. This will be achieved by independent observation of the assessment and patient participant’s responses. This will be assessed on one occasion immediately after observing the response.

Secondary

MeasureTime frame
An assessment of the influence of years in practice, number of shoulder patients assessed and treated each week, and previous training (if any) in the use of the Shoulder Symptoms Modification Procedure.

Countries

Ireland, United Kingdom

Outcome results

None listed

Source: ISRCTN (via WHO ICTRP) · Data processed: Feb 28, 2026