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Comparing Mobilization Techniques for the Hemiplegic Shoulder

Comparing Mobilization Techniques for the Hemiplegic Shoulder

Status
Completed
Phases
NA
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT03211364
Enrollment
11
Registered
2017-07-07
Start date
2016-05-01
Completion date
2017-11-07
Last updated
2017-11-24

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

Conditions

Hemiplegic Shoulder, Mobility Limitation

Brief summary

One of the main complications after stroke is hemiplegic shoulder pain. It is known that one of the most frequent causes of hemiplegic shoulder pain is a restricted range of motion in the shoulder joint. Therefore, it is necessary to preserve the passive range of motion by using the most optimal mobilization technique. The aim of this study is to compare 2 different techniques in order to document their influence on shoulder range of motion and shoulder pain in stroke patients.

Interventions

Comparing the effect of angular mobilization in frontal or scapular plane and of providing soft tissue techniques on hemiplegic shoulder range of motion and pain.

Sponsors

University Ghent
Lead SponsorOTHER

Study design

Allocation
RANDOMIZED
Intervention model
CROSSOVER
Primary purpose
TREATMENT
Masking
SINGLE (Subject)

Masking description

Patients do not know what are the intervention techniques or what is the control technique.

Eligibility

Sex/Gender
ALL
Age
18 Years to No maximum
Healthy volunteers
No

Inclusion criteria

* First stroke * Upper limb impairment

Exclusion criteria

* Shoulder pain on the hemiplegic side with onset before the stroke * Surgery at the hemiplegic shoulder * Active movement possible within the whole range of motion

Design outcomes

Primary

MeasureTime frameDescription
Range of motion of the shoulder using goniometryMeasuring every 4 weeks up to 12 weeks after admission to the study protocolRange of motion of the shoulder joint is measured using a goniometer
Shoulder pain using visual analogue scaleMeasuring every 4 weeks up to 12 weeks after admission to the study protocolShoulder pain during rest, night and activities by using visual analogue scale (0-10)

Secondary

MeasureTime frameDescription
Spasticity of the shoulder muscles using the Modified Ashworth ScaleMeasuring every 4 weeks up to 12 weeks after admission to the study protocolSpasticity of upper limb muscles related to the shoulder using Modified Ashworth Scale
Trunk Impairment Scale to assess trunk stabilityMeasuring every 4 weeks up to 12 weeks after admission to the study protocolTrunk stability using the Trunk Impairment Scale
Fugl-Meyer Assessment - upper limb part to assess voluntary muscle activityMeasuring every 4 weeks up to 12 weeks after admission to the study protocolvoluntary muscle activity upper limb using the upper limb part of the Fugl-Meyer Scale

Countries

Belgium

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 4, 2026