N/A
N=30
Effects Of Sensory Training and Electrical Stimulation on Sole of The Foot Sensations in Patients With Acute Hemiplegia
Hemiplegia · Stroke, Acute · Sensory Disorders
Bottom Line
View on ClinicalTrials.gov: NCT04252092 ↗Enrolled (actual)
30
Serious AEs
—
Results posted
Aug 2020
Primary outcome: Primary: Assessment Of Joint Position Sense — 5.0; 6.4; 8.1; 8.6 correct responses
Study Design & Population
- Study type
- Interventional
- Phase
- N/A
- Interventions
- Sensory training (Other); Electrical stimulation (Other)
- Age
- Adult, Older Adult · 50+ yrs
- Sex
- All
- Sponsor
- Yeditepe University
- Primary completion
- Apr 2020
Outcome Measures
| Outcome | Result | p-value |
|---|---|---|
| PRIMARY Assessment Of Joint Position Sense |
5.0; 6.4; 8.1; 8.6 | — |
| PRIMARY Assesment of Joint Passive Motion Sense |
5.3; 6.8; 8.4; 8.5 | — |
| PRIMARY Assessment of Vibration Sense |
2.5; 4.2; 6.6; 6.4 | — |
| PRIMARY Assesment of Deep Pain Sense |
66.7; 53.3; 13.3; 6.7 | — |
| PRIMARY Assessment of Two-point Discrimination |
7.5; 6.9; 3.1; 3.6 | — |
| PRIMARY Assessment of Graphesthesia |
3.9; 3.1; 6.8; 5.7 | — |
| PRIMARY Assessment of Tactile Localization Sense |
6.3; 7.1; 8.7; 8.8 | — |
| PRIMARY Assessment of Tactile Inattention |
60; 26.7; 20; 13.3 | — |
| SECONDARY Assessment Of Cognitive Level |
23; 22.9 | — |
Summary
The aim of this study is to investigate the effects of the sole of foot sensory education and electrical stimulation on proprioceptive and cortical senses in patients with acute hemiplegia.
Eligibility Criteria
Inclusion Criteria
- Participating to the study in a voluntary basis
- Patients with 50-80 years old
- A stroke diagnosis by a neurologist
- A stroke attack within 6 months
- Minimum 18 points from Mini Mental Test
- Medically stable
Exclusion Criteria
- Unstable condition
- Other neurological or orthopaedic problems that will affect function other than stroke
- Uncontrolled hypertension
- Diabetic foot ulcers
- Part/total foot amputation
Data sourced from ClinicalTrials.gov (NCT04252092). Outcome figures and adverse-event rates are extracted automatically from the registry's posted results and are provided for clinician reference, not as a substitute for the primary publication.