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Effects of Task-Oriented Training Under Different Priming Effects on Upper Limb Dysfunction and Activities of Daily Living in Stroke Patients

Effects of Task-Oriented Training Under Different Priming Effects on Upper Limb Dysfunction and Activities of Daily Living in Stroke Patients

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
ChiCTR
Registry ID
ChiCTR2500097683
Enrollment
Unknown
Registered
2025-02-24
Start date
2023-12-15
Completion date
Unknown
Last updated
2025-03-03

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

Conditions

stroke

Interventions

Group 1: Mirror Therapy combined with Task-Oriented Training:Mirror therapy combined with upper limb task-oriented training, once per day, five times a week, for three weeks.
Group 2: Functional Electrical Stimulation combined with Task-Oriented Training :Upper limb functional electrical stimulation combined with task-oriented training, once per day, five times a week, for
Control group: Task-oriented group:The control group underwent task-oriented training only, once per day, five times a week, for three weeks.

Sponsors

Zhongda Hospital, Southeast University
Lead Sponsor

Eligibility

Sex/Gender
All
Age
18 Years to 80 Years

Inclusion criteria

Inclusion criteria: (1) Meets the diagnostic criteria for stroke in the "Diagnostic Key Points for Various Cerebrovascular Diseases" and is confirmed by CT or MRI brain scans; (2) First occurrence of stroke, with the disease duration ranging from 2 weeks to 6 months, and stable vital signs; (3) Aged >= 18 years; (4) No severe upper limb spasticity (Modified Ashworth Scale scores < 3); (5) Cognitive level sufficient to follow instructions; (6) Willing to cooperate with the study and sign the informed consent form.

Exclusion criteria

Exclusion criteria: Exclusion criteria: (1) Patients with severe spasticity who have not received treatment; (2) Presence of metallic implants at the site of electrical stimulation; (3) Patients with severe cognitive impairment or mental disorders; (4) Severe cardiopulmonary insufficiency; (5) Patients with no sensation or severe allergy to electrical stimulation; (6) Patients with a history of botulinum toxin injection within the past three months; (7) Patients with severe visual or visuoperceptual disorders, such as severe hemispatial neglect or hemianopia; (8) Accompanying neurological, neuromuscular, or orthopedic diseases, such as brain tumors or Parkinson's disease.

Design outcomes

Primary

MeasureTime frame
Fugl-Meyer Assessment-Upper Extremities;

Secondary

MeasureTime frame
Motor Evoked Potential, MEP;near-infrared brain imaging;surface electromyography (sEMG);Barthel Index;Motor Activity Log(MAL);

Countries

China

Contacts

Public ContactXiangshan Wei

Zhongda Hospital, Southeast University

3242975593@qq.com+86 177 1598 5899

Outcome results

None listed

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