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Research on multisensory stimulation in patients with post-stroke sleep disorders

Multi-Sensory Stimulation Therapy Improves Sleep and Cognition in Post-Stroke Sleep Disorders (PSSD): A Randomized Trial

Status
Active, not recruiting
Phases
Early Phase 1
Study type
Interventional
Source
ChiCTR
Registry ID
ChiCTR2500105608
Enrollment
Unknown
Registered
2025-07-07
Start date
2025-02-03
Completion date
Unknown
Last updated
2025-07-14

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

Conditions

Post-Stroke Sleep Disorders

Interventions

MSSTgroup:including 4 units (such as visual, tactile, olfactory, and gustatory) based on the patients tolerance. Each unit includes 1 health education session and =5 training sessions per week
control group:conventional nursing care such as drug treatment and basic rehabilitation training

Sponsors

The Second Affiliated Hospital of Army Medical University
Lead Sponsor

Eligibility

Sex/Gender
All
Age
60 Years to 100 Years

Inclusion criteria

Inclusion criteria: 1 Age >= 60 years old, meeting the newly revised diagnostic criteria for ischemic stroke by the Neurology Society of Chinese Medical Association, and confirmed by CT or MRI; 2 mRs >= 3 points; 3 No organ dysfunction such as heart, liver, or kidney; stable vital signs; 4 Mini-Mental State Examination (MMSE) score: MMSE > 20 points for those with primary school or lower education level, and MMSE > 24 points for those with junior high school or higher education level; 5 Informed consent, and voluntary participation in this study.

Exclusion criteria

Exclusion criteria: 1 Acute stage of stroke; 2 Individuals who had sleep disorders before the onset; 3 Those with visual, auditory or expressive impairments that affected the conduct of the study; 4 Those with a known allergy to any component of the multi-sensory stimulation training; 5 Those with severely reduced visual and auditory abilities and poor sense of smell; 6 Those with severe mental and psychological disorders resulting in difficulty in following instructions; 7 Those with poor vision or poor cooperation; 8 Those who participated in other clinical trials or studies that might affect the results of this study.

Design outcomes

Primary

MeasureTime frame
sleep quality;

Secondary

MeasureTime frame
cognitive function;quality of life;

Countries

China

Contacts

Public ContactQin Li

The Second Affiliated Hospital of Army Medical University

liqin8311@yeah.net+86 136 9641 8919

Outcome results

None listed

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