Efficacy and safety of neuromuscular electrical stimulation for prevention-improvement of stress injuries in bedridden stroke patients

Status

Active, not recruiting

Phases

Early Phase 1

Study type

Interventional

Source

ChiCTR

Registry ID

ChiCTR2400081502

Enrollment

Unknown

Registered

2024-03-04

Start date

2024-04-01

Completion date

Unknown

Last updated

2024-03-11

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

Conditions

Pressure injury

Interventions

Routine nursing group:Routine care measures

NMES group:Routine nursing measures and NMES applied to the sacrococcygeal region

Eligibility

Sex/Gender

All

Age

18 Years to 75 Years

Inclusion criteria

Inclusion criteria: ? Patients aged 18-75 who have been diagnosed with stroke through CT or MRI. ?The patient or guardian agrees to sign the informed consent for the trial. ? The onset time was within one month and there was no sacrococcygeal pressure injury. ?The patient lacks the ability to autonomously roll, stand, and transfer movements, and requires assistance to complete the above actions.

Exclusion criteria

Exclusion criteria: ? Pregnancy, pacemaker or defibrillator implantation; ? Preexisting neuromuscular diseases (Duchenne's disease, myasthenia gravis, Guillain Barre syndrome), brain death, spinal cord injury, BMI greater than or equal to 35 km/m2, rhabdomyolysis, skin injury at electrode application site, or medical contraindications.

Design outcomes

Primary

Measure	Time frame
Incidence of pressure injuries;Waterlow pressure sore risk assessment scale;Barden Assessment Form;	—

Countries

China

Contacts

Public ContactWeili Zhu

Yuebei People's Hospital

416510988@qq.com+86 189 2259 9170

Outcome results

None listed

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