Skip to content

Evaluating the effect of a dynamic shoulder subluxation orthosis on shoulder pain and shoulder subluxation

Evaluating the effect of a dynamic shoulder subluxation orthosis on shoulder pain and shoulder subluxation - Evaluation of a dynamic shoulder subluxation orthosis

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
NL-OMON
Registry ID
NL-OMON49685
Enrollment
13
Registered
2020-10-12
Start date
2021-02-13
Completion date
Unknown
Last updated
2024-04-09

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

Conditions

partial dislocation of the shoulder joint shoulder subluxation

Interventions

The study population is provided a shoulder orthosis for the duration of two weeks. In the week before the orthosis fitting, the population will not use any intervention.

Sponsors

Universiteit Twente
Lead Sponsor

Eligibility

Age
18 Years to 99 Years

Inclusion criteria

Inclusion criteria: - >= 18 years - Suspicion of subluxation of the glenohumeral joint - Chronic shoulder pain (> 6 months) - Having given written informed consent prior to undertaking any study-related procedures

Exclusion criteria

Exclusion criteria: - Unable to understand and follow simple verbal commands - Inability to sit upright in a chair without arm supports for at least 15 minutes consecutively - Inability to let the affected arm unsupported for one week - Irritated skin in the application area of the orthosis - Recent shoulder or arm operation (

Design outcomes

Primary

MeasureTime frame
The main study parameters are: (1) the shoulder pain scores before and during the intervention, and (2) the acromiohumeral distance without and with orthosis.

Secondary

MeasureTime frame
The secondary study parameters are: pain-free range of motion, arm activity, shoulder function, device usage and user satisfaction

Countries

Netherlands

Outcome results

None listed

Source: NL-OMON (via WHO ICTRP)