Efficacy of Mulligan's mobilization with movement techniques on hemiplegic shoulder pain

Status

Recruiting

Phases

Early Phase 1

Study type

Interventional

Source

ChiCTR

Registry ID

ChiCTR2000039522

Enrollment

Unknown

Registered

2020-10-30

Start date

2020-11-01

Completion date

Unknown

Last updated

2021-02-01

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

Conditions

stroke

Interventions

control group:conventional rehabilitation treatments (CRT)

experimental group:CRT+MWM

Eligibility

Sex/Gender

All

Age

18 Years to 75 Years

Inclusion criteria

Inclusion criteria: (1) Clinical diagnosis of hemiplegic shoulder pain. (2) Aged from 18 to 75 years,male and female. (3) The presence of HSP lasted more than one month. (4) The Brunnstrom Scale >= IV. (5) The mini-mental state examination (MMSE) score >= 24. (6) The visual analogue scale (VAS) score > 4. (7) Patients being able to provide informed consent.

Exclusion criteria

Exclusion criteria: (1) MRI examination showed severe rotator cuff or biceps tendon tear of the patients needing surgery. (2) Had a history of chronic shoulder pain or had undergone shoulder surgery before stroke. (3) Had complex regional pain syndrome after stroke. (4) Had severe sensory dysfunciton on the affected side. (5) Spasticity of 2 or more points as determined by the Modified Ashworth Scale (MAS).

Design outcomes

Primary

Measure	Time frame
visual analogue scale (VAS);	—

Secondary

Measure	Time frame
range of motion (ROM);Chinese version of the Constant-Murley questionnaire for shoulder pain and disability (CMS);Fugl-Meyer assessment scale of upper extremity (FMA-UE);	—

Countries

China

Contacts

Public ContactPei Ziwen

Wuhan NO.1 Hospital

165592510@qq.com+86 13296666644

Outcome results

None listed

Source: ChiCTR (via WHO ICTRP) · Data processed: Feb 4, 2026