Skip to content

The influence of dual-task training combined with virtual reality upper limb rehabilitation robot on upper limb function and activities of daily living ability of stroke patients

The influence of dual-task training combined with virtual reality upper limb rehabilitation robot on upper limb function and activities of daily living ability of stroke patients

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
ChiCTR
Registry ID
ChiCTR2600116543
Enrollment
Unknown
Registered
2026-01-12
Start date
2026-01-13
Completion date
Unknown
Last updated
2026-01-27

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

Conditions

Stroke

Interventions

control group:Provide routine occupational therapy training
Dual-task group:Based on the occupational therapy of the control group, cognitive instructions were integrated to conduct motor and cognitive dual-task training
Combined Group:Based on the dual-task group treatment plan, virtual reality upper limb rehabilitation robot training is added

Sponsors

North China University of Science and Technology;The Affiliated Hospital of North China University of Science and Technology
Lead Sponsor

Eligibility

Sex/Gender
All
Age
18 Years to 80 Years

Inclusion criteria

Inclusion criteria: 1.The diagnosis is in line with the "Key Points for Diagnosis of Various Cerebrovascular Diseases" formulated by the Fourth National Cerebrovascular Disease Conference 2.Age range: 18 to 80 years old. 3.Disease duration 17 points, primary school > 20 points, junior high school and above > 24 points. Patients with severe cognitive impairment are excluded. The Montreal Cognitive Assessment (MoCA) score>= 18 points. 5. Inpatients or outpatients with stroke at Brunnstrom stage II-? and Modified Barthel Index (MBI) score of 20-70 points. 6.Patients who have signed informed consent and voluntarily participated.

Exclusion criteria

Exclusion criteria: 1.Those with severe complications or other diseases who cannot participate; 2.Those with severe mental disorders or who disagree to participate for various reasons; 3. Those with severe spasticity (modified Ashworth >= grade 3) or combined with other neurological diseases; 4.Those with severe heart, liver or kidney diseases or bone and joint diseases that affect movement.

Design outcomes

Primary

MeasureTime frame
Fugl-Meyer Assessment of Upper Extremity Scale;modifide barthle index;

Secondary

MeasureTime frame
Jebsen Taylor Hand Function Test;Action Research Arm;Grip strength tester;the trail making test;Dual-task cost;

Countries

China

Contacts

Public ContactZhao Yaning; Xue Xinhong;Wang Yirong

North China University of Science and Technology;The Affiliated Hospital of North China University of Science and Technology

13789199186@163.com+86 137 8919 9186

Outcome results

None listed

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