The Effects of IASTM and Proprioception

NCT ID: NCT03023943

Last Updated: 2020-01-10

Study Results

Results pending

The study team has not published outcome measurements, participant flow, or safety data for this trial yet. Check back later for updates.

Basic Information

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Recruitment Status

COMPLETED

Clinical Phase

NA

Total Enrollment

30 participants

Study Classification

INTERVENTIONAL

Study Start Date

2017-02-03

Study Completion Date

2018-05-31

Brief Summary

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The research design will be single group pretest-posttest design. The subject will be instructed to position the knee joint to a position previously set by the experimenter. Intervention will be 10 minutes of GT1 instrument application at anterior thigh using sweep technique.

Detailed Description

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Conditions

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Healthy Volunteers

Study Design

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Allocation Method

NA

Intervention Model

SINGLE_GROUP

Primary Study Purpose

TREATMENT

Blinding Strategy

NONE

Study Groups

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IASTM group

Intervention will be 10 minutes of GT1 instrument application at anterior thigh using sweep technique.

Group Type EXPERIMENTAL

Instrument Assisted Soft Tissue Mobilization

Intervention Type OTHER

Intervention will be 10 minutes of GT1 instrument application at anterior thigh using sweep technique.

Interventions

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Instrument Assisted Soft Tissue Mobilization

Intervention will be 10 minutes of GT1 instrument application at anterior thigh using sweep technique.

Intervention Type OTHER

Other Intervention Names

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IASTM

Eligibility Criteria

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Inclusion Criteria

* male or female, age 18 to 65.

Exclusion Criteria

* sensory impairments or a present contraindications to IASTM which include cancer, burn scars, kidney dysfunction, pregnancy, varicose veins, osteoporosis, body art, chronic regional pain syndrome, polyneuropathies, fractures, autoimmune disorders, diabetes, vitamin C \& D/Calcium deficiencies, rheumatoid arthritis, ankylosing spondylitis, congestive heart failure, acute inflammation, lymphedema, flu or illness with flu-like symptoms, and medications (anticoagulant, steroids, hormone replacements, NSAIDS, fluoroquinolone antibiotics, herbal supplements).
Minimum Eligible Age

18 Years

Maximum Eligible Age

65 Years

Eligible Sex

ALL

Accepts Healthy Volunteers

Yes

Sponsors

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Youngstown State University

OTHER

Sponsor Role lead

Responsible Party

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Weiqing Ge

Associate Professor

Responsibility Role PRINCIPAL_INVESTIGATOR

Principal Investigators

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Michael Hripko

Role: STUDY_DIRECTOR

Youngstown State University

Locations

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Youngstown State University

Youngstown, Ohio, United States

Site Status

Countries

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United States

Other Identifiers

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072-2017

Identifier Type: -

Identifier Source: org_study_id

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