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A randomized controlled trial of high-intensity walking training combined with step counting monitoring for improving walking activity in patients with chronic stroke

A randomized controlled trial of high-intensity walking training combined with step counting monitoring for improving walking activity in patients with chronic stroke

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
ChiCTR
Registry ID
ChiCTR2600123031
Enrollment
Unknown
Registered
2026-04-21
Start date
2026-05-06
Completion date
Unknown
Last updated
2026-04-27

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

Conditions

Stroke

Interventions

FAST group (high-intensity walking training group):30 minutes of treadmill training (heart rate controlled at 70%-80% heart rate reserve) + 10 minutes of ground training (turning around, going up and
slow down the speed when fatigued or heart rate exceeds the standard, and adjust the intensity after recovery.
SAM group (step counting monitoring group):Wear a domestic smart wristband (basic model of Xiaomi/Huawei) on the non-stroke side wrist, set the initial target according to the average step count in th
FAST+SAM group (combined intervention group):Receive all the training of the FAST group and all the step counting monitoring and guidance of the SAM group at the same time, complete 30 minutes of FAST

Sponsors

Nantong Haimen People's Hospital
Lead Sponsor

Eligibility

Sex/Gender
All
Age
21 Years to 85 Years

Inclusion criteria

Inclusion criteria: Aged 21-85 years, at least 6 months after a stroke, able to walk independently, less than 8,000 steps per day, physically safe, mentally clear, signed informed consent.

Exclusion criteria

Exclusion criteria: Cerebellar stroke / other neurological diseases, recent lower limb botulinum toxin injection, currently undergoing other physical therapy, unable to walk before stroke, recent history of cardiac surgery, unable to communicate in Chinese / cognitive impairment, unable to use a pedometer independently.

Design outcomes

Primary

MeasureTime frame
Daily step count;

Secondary

MeasureTime frame
6-minute walking distance;10-meter walking speed;resting heart rate;blood pressure;

Countries

China

Contacts

Public ContactJiawen Lu

Nantong Haimen People's Hospital

pollux_lu@163.com+86 137 7365 6789

Outcome results

None listed

Source: ChiCTR (via WHO ICTRP) · Data processed: May 1, 2026