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Study on rehabilitation nursing methods for patients with stroke shoulder pain

Construction and effect evaluation of rehabilitation nursing intervention program for stroke patients with hemiplegia and shoulder pain based on ICF theory

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
ChiCTR
Registry ID
ChiCTR2500112096
Enrollment
Unknown
Registered
2025-11-10
Start date
2025-04-17
Completion date
Unknown
Last updated
2025-11-17

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

Conditions

Hemiplegic shoulder pain ( HSP )

Interventions

interventional group:Rehabilitation nursing program based on ICF framework
control group:Routine rehabilitation nursing measures

Sponsors

Shenzhen Nanshan People's Hospital
Lead Sponsor

Eligibility

Sex/Gender
All
Age
35 Years to 85 Years

Inclusion criteria

Inclusion criteria: 1. In line with the ' Chinese Guidelines for the Diagnosis and Treatment of Cerebrovascular Diseases ' stroke diagnostic criteria ; 2. The affected upper limb Brunnstrom stage >= 2, hand Brunnstrom stage >= 1. 3. No obvious cognitive impairment ( MMSE > 21 points ) ; 4. Unilateral hemiplegia with spontaneous shoulder pain or active shoulder pain ( pain score >= 5 ) ; 5. Voluntary signed informed consent and cooperate with the treatment plan. 6. Age 35-85 years;

Exclusion criteria

Exclusion criteria: 1. Transient ischemic attack (TIA) or reversible neurological deficit (RIND); 2. There was a history of shoulder joint trauma, surgery or chronic shoulder pain before stroke ; 3. Non-stroke-related shoulder pain ( including but not limited to ) : periarthritis of shoulder ( adhesive capsulitis, rotator cuff injury / calcific tendinitis, rheumatoid arthritis / cervical nerve root disease, thalamic pain syndrome / complex regional pain syndrome, tumor metastatic pain ; 4. Patients with severe respiratory and cardiovascular diseases ; mental illness or cognitive impairment can not cooperate with treatment ; 5. Received shoulder joint closure treatment in the past 3 months ; 6. Participate in other interventional clinical trials during the study period ; 7. Unwilling to participate in this study.

Design outcomes

Primary

MeasureTime frame
Fugl-Meyer Assessment for Upper Extremity Motor Function (FMA-UE);NRS pain score;

Secondary

MeasureTime frame
Modified Barthel Index, MBI;Generalized Anxiety Disorder-7 (GAD-7) Scale;

Countries

China

Contacts

Public ContactMo Beirong

Shenzhen Nanshan People's Hospital

limo1997@163.com+86 755 2655 3111

Outcome results

None listed

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