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Clinical Trial Details — Status: Not yet recruiting

Administrative data

NCT number NCT03675958
Other study ID # UISantander
Secondary ID
Status Not yet recruiting
Phase N/A
First received
Last updated
Start date September 24, 2018
Est. completion date March 31, 2019

Study information

Verified date September 2018
Source Universidad Industrial de Santander
Contact Maria Juliana González Silva
Phone (057) + 3166208712
Email majugonza@hotmail.com
Is FDA regulated No
Health authority
Study type Interventional

Clinical Trial Summary

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.


Recruitment information / eligibility

Status Not yet recruiting
Enrollment 20
Est. completion date March 31, 2019
Est. primary completion date December 15, 2018
Accepts healthy volunteers No
Gender All
Age group 50 Years to 70 Years
Eligibility 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.

Study Design


Intervention

Other:
Johnstone's Pressure Splint
the intervention consists in the application of two tools used for the treatment of spasticity post - CVD. Johnstone's Pressure Splint added Stretching
Stretching
the intervention consists in the application of one tool used for the treatment of spasticity post - CVD. Just Stretching

Locations

Country Name City State
n/a

Sponsors (1)

Lead Sponsor Collaborator
Universidad Industrial de Santander

Outcome

Type Measure Description Time frame Safety issue
Primary Muscular tone of wrist and elbow flexors. Defined as the resistance to movement of passive movement, it will be evaluated by the Modified Ashworth Scale (EAM) in flexo-extensors of the elbow and wrist and hand. (Ordinal scale of 6 points, with a range from 0 = normal tone to 4 = rigid segment in flexion or extension) .109 The EAM includes an additional degree of 1+, which has a sub-classification between an increase level and an increase of speed in the tone. before (baseline) and immediately after the intervention (maximum 10 minutes after the intervention).
Primary Reflex excitability of the flexor carpi radialis. Excitability is a specific property of muscle and nerve tissue and occurs when depolarization exceeds the threshold level in the action potential. The excitability will be measured from the evocation of H Reflex in the flexor carpi radialis muscle (FRC). before (baseline) and immediately after the intervention (maximum 10 minutes after the intervention).
Primary Joint kinematics in Functional Reach Pattern 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. before (baseline) and immediately after the intervention (maximum 10 minutes after the intervention).
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