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Cross-Education and Mirror Therapy for Upper Limb in Post-Stroke Patients

Not Applicable
Recruiting
Conditions
Stroke
Interventions
Other: Cross-education
Other: Conventional Physical Therapy
Other: Mirror therapy
Registration Number
NCT05920031
Lead Sponsor
Ahram Canadian University
Brief Summary

This randomized controlled trial will investigate the potential synergistic effects of combining cross-education training with mirror therapy on strength and motor function in the more affected upper limb of post-stroke patients.

Detailed Description

Not available

Recruitment & Eligibility

Status
RECRUITING
Sex
All
Target Recruitment
100
Inclusion Criteria
  • Post-stroke patients with upper limb motor impairments
  • Aged 30 years to 60 years old
  • At least 3 months post-stroke
  • Able to participate in the intervention
Exclusion Criteria
  • Severe cognitive impairments
  • Visual impairments
  • Any contraindications to the intervention

Study & Design

Study Type
INTERVENTIONAL
Study Design
PARALLEL
Arm && Interventions
GroupInterventionDescription
Cross-education training onlyCross-educationParticipants will perform resistance exercises at 60% of their 1 repetition maximum (1RM) with the less affected limb.
Combined cross-education and mirror therapyMirror therapyParticipants will perform resistance exercises with the less affected limb while observing its reflection in a mirror.
Mirror therapy onlyMirror therapyParticipants will perform bilateral upper limb movements while observing the reflection of the less affected limb in a mirror.
Conventional rehabilitationConventional Physical TherapyParticipants will receive conventional rehabilitation for post-stroke upper limb motor impairments.
Combined cross-education and mirror therapyCross-educationParticipants will perform resistance exercises with the less affected limb while observing its reflection in a mirror.
Primary Outcome Measures
NameTimeMethod
Changes in Upper limb strengthChanges in Upper limb strength at baseline, 8 weeks, 16 weeks

Upper limb strength (measured by hand-held dynamometry)

Changes in motor functionChanges in motor function at baseline, 8 weeks, 16 weeks

motor function (measured by Fugl-Meyer Assessment)

Secondary Outcome Measures
NameTimeMethod
Changes in Quality of lifeChanges in Quality of life at baseline, 8 weeks, 16 weeks

Quality of life (measured by Stroke Impact Scale)

Trial Locations

Locations (1)

Outpatient clinic of faculty of physical therapy, Ahram Canadian University

🇪🇬

Al Ḩayy Ath Thāmin, Giza, Egypt

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