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Clinical Trial Details — Status: Completed

Administrative data

NCT number NCT04023279
Other study ID # UniversidadNAB
Secondary ID
Status Completed
Phase N/A
First received
Last updated
Start date September 24, 2018
Est. completion date December 20, 2018

Study information

Verified date July 2019
Source Universidad Nacional Andres Bello
Contact n/a
Is FDA regulated No
Health authority
Study type Interventional

Clinical Trial Summary

This study evaluated the additive effect of myofascial release therapy on the brachial biceps on conventional management (TENS) in pain intensity, hand prehensile strength and upper limb functionality of individuals with lateral epicondylalgia.


Description:

This study determined the additive effect of the myofascial release therapy of brachial biceps on TENS in the variables pain intensity, hand prehensile strength and upper limb functionality of individuals with lateral epicondylalgia, compared to a group that received only TENS. This was done in a sample of 32 individuals, assigned in two groups: group A that received an application of TENS and group B that received an application of TENS plus myofascial release therapy.

Contrary to the hypothesis, the application of myofascial release therapy added to the application of TENS proved to generate a significant change only in the prehensile hand force with respect to the group that received only TENS.


Recruitment information / eligibility

Status Completed
Enrollment 32
Est. completion date December 20, 2018
Est. primary completion date October 22, 2018
Accepts healthy volunteers No
Gender Female
Age group 30 Years to 50 Years
Eligibility Inclusion Criteria:

- Female between 30 and 50 years old.

- Belong to the administrative staff of the university in question

- Have a symptomatic diagnosis of chronic lateral epicondylitis (> 6 weeks)

Exclusion Criteria:

- Being pregnant

- Have done moderate or intense aerobic or anaerobic sport activities of any kind 72 hours before the registrations

- Have an orthopedic, rheumatologic, neuropsychiatric or associated comorbidities diagnosed.

- Have suffered a fracture or trauma involving the upper extremity 4 months before the intervention.

- Be in medical, pharmacological or kinesthetic treatment during the intervention or 2 weeks before this.

Study Design


Related Conditions & MeSH terms


Intervention

Other:
TENS
100 Hz and 100 usec for 20 minutes
Myofascial therapy
Seven to fifteen transverse sliding repetitions and three repetitions of longitudinal sliding of myofascial release therapy

Locations

Country Name City State
Chile Universidad Andres Bello Talcahuano Concepción

Sponsors (1)

Lead Sponsor Collaborator
Fernanda Merino Alvarez

Country where clinical trial is conducted

Chile, 

Outcome

Type Measure Description Time frame Safety issue
Primary Change in pain intensity numerical rating scale Self-reported measure of pain intensity. It consists on asking to assess pain intensity by selecting a number on a scale of 11 horizontal points. It is represented from 0 (without pain) to 10 (the worst possible pain) A score of 1 to 4 indicates mild pain; 5-6, moderate pain; and 7 to 10, severe pain. One month
Primary Pressure pain threshold Is the minimum pressure that induces pain or discomfort. It was measured with a algometer. It is expressed in units of pressure as kilograms per square centimeter per second (Kg / cm2 / s). Immediately after treatment
Primary Prehensile hand strength It is the ability to compress the hand, related to the functional integrity of the upper extremity as an index of general health. It was measured with a dynamometer. It was measured according to the criteria established by the American Society of Hand Therapists. It is measured in kilograms Immediately after treatment
Primary Change in Elbow functionality. Functionality is a generic term that includes bodily functions, body structures, activities and participation. It shows the positive aspects of a person's interaction and the context. It was obtained through a scale of functionality (Oxford Elbow Score), which is composed of three domains (subscales); elbow, pain and social-psychological function, which underlie 12 questions, which are internally consistent, one-dimensional and do not have redundancy of items.
The scores of each domain are calculated as the sum of the score of each individual element, where each case is expressed on a scale from 0 to 100 where, a score of 0.84 indicates a substantial improvement.
One month
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