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Exploring the effect of acupuncture on rehabilitation outcomes and cost-utility analysis of patients with post-stroke shoulder pain based on real-world data

Exploring the effect of acupuncture on rehabilitation outcomes and cost-utility analysis of patients with post-stroke shoulder pain based on real-world data

Status
Recruiting
Phases
Unknown
Study type
Observational
Source
ChiCTR
Registry ID
ChiCTR2400088386
Enrollment
Unknown
Registered
2024-08-16
Start date
2024-08-16
Completion date
Unknown
Last updated
2024-08-19

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

Conditions

post-stroke shoulder pain

Interventions

Acupuncture group (exposed group, Documentation of acupuncture treatments for patients with post-stroke shoulder pain in a hospital. The treatment protocol indicated the time of treatment, stimulation
Acupuncture-free group (Record the hospital's routine rehabilitation treatment programme for patients with post-stroke shoulder pain (including microwave therapy, ultrasound therapy, exercise therapy,

Sponsors

Affiliated Rehabilitation Hospital of Fujian University of Traditional Chinese Medicine
Lead Sponsor

Eligibility

Sex/Gender
All
Age
18 Years to 100 Years

Inclusion criteria

Inclusion criteria: ? Meet the diagnostic criteria of stroke (refer to the diagnostic criteria of ‘Stroke’ in the ‘China Clinical Management Guidelines for Cerebrovascular Diseases’ and confirmed by neuroimaging examination such as CT or MRI); ? Accompanied by shoulder pain; ?The duration of the disease is more than 14 days;

Exclusion criteria

Exclusion criteria: ?People who have been examined and confirmed to have frozen shoulder, cervical spondylosis, brain tumour, traumatic brain injury, cerebral parasitosis, and other diseases that can cause shoulder pain; ? Cerebral haemorrhage or acute stage of cerebral infarction; ?History of alcohol and drug abuse; Excluding patients with severe cognitive dysfunction; ? Participating in other clinical trials that affect the evaluation of the results of this study;

Design outcomes

Primary

MeasureTime frame
VAS pain score;Range of motion (ROM) of the shoulder joint;

Secondary

MeasureTime frame
Fugl-Meyer scale;Modified Barthel Index Scale (MBI);satisfaction scale;Shoulder Pain and Dysfunction Index (SPADI);Incremental cost-effectiveness ration,ICER;

Countries

China

Contacts

Public ContactChen Jincheng

Affiliated Rehabilitation Hospital of Fujian University of Traditional Chinese Medicine

494336046@qq.com+86 136 9685 5306

Outcome results

None listed

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