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The impact of multidisciplinary collaborative rehabilitation based on wearable devices on physical activity and sedentary self-efficacy in patients with acute ischemic stroke: a randomized controlled trial

The impact of multidisciplinary collaborative rehabilitation based on wearable devices on physical activity and sedentary self-efficacy in patients with acute ischemic stroke: a randomized controlled trial

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
ChiCTR
Registry ID
ChiCTR2600120232
Enrollment
Unknown
Registered
2026-03-11
Start date
2026-03-17
Completion date
Unknown
Last updated
2026-03-16

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

Conditions

Acute ischemic stroke

Interventions

Control group:Receive standard rehabilitation care, including basic physical therapy: 3 sessions per week, each lasting 30 minutes, focusing on basic functional training
health education: one collective online lecture per week, covering stroke prevention and general activity recommendations.
Intervention group:Based on conventional rehabilitation, patients receive a multidisciplinary collaborative rehabilitation program utilizing wearable devices. The multidisciplinary team consists of ne

Sponsors

Longyou County People's Hospital
Lead Sponsor

Eligibility

Sex/Gender
All
Age
18 Years to No maximum

Inclusion criteria

Inclusion criteria: 1.Meet the above diagnostic criteria, aged >=18 years, of either gender; 2.Have had an ischemic stroke for <=10 days; 3. Present with limb movement impairment, and a modified Rankin Scale (mRS) score of 2-5; 4.Have signed the informed consent form.

Exclusion criteria

Exclusion criteria: 1. Previously having a history of stroke, or having other reasons (such as limb movement dysfunction caused by claudication, osteoarthritis, rheumatoid arthritis, gouty arthritis, fractures, etc. before the study) leading to limb dysfunction, resulting in an mRS score of >=2 before the onset of this disease; 2. Large-area cerebral infarction (CT indicates involvement of more than one lobe or more than 1/3 of the blood supply area of the middle cerebral artery) accompanied by severe brain edema, space-occupying effect, and signs of brain herniation, or requiring surgical treatment; 3. Currently participating in or having participated in other clinical studies and the end of the study is less than 3 months ago.

Design outcomes

Primary

MeasureTime frame
Reduce self-efficacy of sedentary behavior;

Secondary

MeasureTime frame
6-minute walk test;Stand up and sit down timing test;Skeletal muscle content of limbs;Fugl-Meyer Assessment Scale (Lower Extremity);

Countries

China

Contacts

Public ContactZhou Wangqing

Longyou County People's Hospital

1442881225@qq.com+86 150 5857 8010

Outcome results

None listed

Source: ChiCTR (via WHO ICTRP) · Data processed: Mar 20, 2026