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Immediate Effect of Johnstone's Pressure Splint Added to Stretching on the Spasticity in Cerebrovascular Disease.

U

Universidad Industrial de Santander

Status

Unknown

Conditions

Spasticity as Sequela of Stroke

Treatments

Other: Johnstone's Pressure Splint
Other: Stretching

Study type

Interventional

Funder types

Other

Identifiers

NCT03675958
UISantander

Details and patient eligibility

About

TITLE: Immediate effect of Johnstone's Pressure Splint added to Stretching on the spasticity of elbow flexors and wrist in Cerebrovascular Disease (CVD).

INTRODUCTION: In the rehabilitation of the upper limb post-CVD to employed exercise modalities such as stretching (S) to control spasticity, improve mobility and functionality. Also it is used the Johnstone´s Pressure Splint (JPS), which exerts circumferential pressure and contribute to spastic pattern inhibition, sensory re-education and increased of the mobility.

OBJECTIVE: The aim of the study is to evaluate the immediate effect of JPS added to S on the spasticity of elbow flexors and wrist, the reflex excitability and the joint kinematics in Stroke.

MATERIALS AND METHODS: A randomized experimental study with two intervention groups will be performed. Control group (GS): Stretching and experimental group: (GJPS + S): JPS plus S. Measurement times: Before the intervention (T0) and immediately post- intervention (T1). The outcome variables are muscle tone of elbow, wrist and hand assessed with the Modified Ashworth Scale (MAS); H reflex of the Flexor Carpi Radialis muscle, latency (ms), duration (ms) and amplitude (mV) of the M and H waves, and the amplitude the Hmax / Mmax ratio (%). Shoulder, elbow and trunk angles (degrees), trunk displacement (cm) and duration (sec) of the Functional Reach Pattern (PAF) will be evaluated with the software Contemplas.

ANALYSIS: Descriptive statistics will be applied and Shapiro Wilk test to evaluate the normality of the variables. Intra-group differences will be assessed with the student t-test paired and intergroup with the student t-test unpaired or the sum of Wilcoxon rank according to the distribution of the variables.

EXPECTED RESULTS: Hypotheses and contributions to the scientific evidence on the immediate effect of the S and JPS will be generated, to support the JPS as a complement to the traditional treatment. The results will be socialized in an international scientific event and a publication will be submitted to an impact journal.

KEY WORDS: Spasticity, H Reflex, Johnstone's Pressure Splint, Stretching, Functional Reach.

Enrollment

20 estimated patients

Sex

All

Ages

50 to 70 years old

Volunteers

No Healthy Volunteers

Inclusion criteria

  • Medical diagnosis of CVD.
  • Minimum evolution time from 6 months to 48 months.
  • Muscular tone according to the Modified Ashworth Scale> a 1+ in the elbow and wrist flexors.
  • Maintain seated position without human support or assistance for at least 10 seconds and maintain standing position for more than 30 seconds to perform transfers from one surface to another.

Exclusion criteria

  • Altered cognitive ability, assessed through the "Short Portable Mental State Questionnaire".
  • Application of botulinum toxin within six (6) months prior to participation in the study.
  • Patients with skin lesions, lacerations or allergies.
  • People with pacemaker.
  • People in whom the H reflex can not be evoked.
  • Pain and hyperalgesia in the upper limb.
  • Peripheral vascular disease in upper limb.
  • Fractures, or musculoskeletal injuries in the paretic upper limb less than a year old.
  • Osteoarthritis, rheumatoid arthritis and clinical conditions associated with acute pain, inflammation, and moderate to severe decrease in joint mobility.
  • Consumption of drugs such as Baclofen, benzodiazepines, or muscle relaxants such as dantrolene and tizanidine.
  • Ingestion of caffeine and alcohol 12 hours before evaluations.

Trial design

Primary purpose

Treatment

Allocation

Randomized

Interventional model

Parallel Assignment

Masking

Single Blind

20 participants in 2 patient groups

GJPS + S
Experimental group
Description:
Experimental group: (GJPS + S) : Application Johnstone´s Pressure Splint plus Stretching in in 4 different treatment postures.
Treatment:
Other: Johnstone's Pressure Splint
Other: Stretching
GS
Active Comparator group
Description:
Control group (GS): Just Stretching in 4 different treatment postures.
Treatment:
Other: Stretching

Trial contacts and locations

0

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Central trial contact

Maria Juliana González Silva

Data sourced from clinicaltrials.gov

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