EFFECTS OF ACUPUNCTURE ON LEG MUSCLE STRENGTH

October 7, 2021 updated by: Wahyuningsih Djaali, Indonesia University

EFFECTS OF ACUPUNCTURE ON LEG MUSCLE STRENGTH: RANDOMIZED CONTROLLED TRIAL IN SPORTS STUDENTS

Press tack needle is one of the acupuncture modalities in the form of needles that are attached to the skin, and can be left attached to the skin for several days which makes its use much easier than conventional acupuncture.

The purpose of this study was to determine how the effect of press tack needle acupuncture on leg muscle strength performed on sports students.

Research subjects as many as 30 people were randomized into two groups, namely the intervention group and the control group. In the intervention group, acupuncture treatment was performed with a press tack needle at acupuncture points on the legs. The leg muscle strength was measured using a leg dynamometer before and after the acupuncture intervention. Analyzed the difference in mean leg muscle strength before and after the intervention, and between the two groups.

Study Overview

Status

Completed

Study Type

Interventional

Enrollment (Actual)

30

Phase

  • Not Applicable

Contacts and Locations

This section provides the contact details for those conducting the study, and information on where this study is being conducted.

Study Locations

      • Jakarta, Indonesia
        • Sport Science Faculty, Universitas Negeri Jakarta

Participation Criteria

Researchers look for people who fit a certain description, called eligibility criteria. Some examples of these criteria are a person's general health condition or prior treatments.

Eligibility Criteria

Ages Eligible for Study

18 years to 25 years (Adult)

Accepts Healthy Volunteers

Yes

Genders Eligible for Study

Male

Description

Inclusion Criteria:

  • willingness to fill out an informed consent form;
  • age between 18-25 years;
  • male;
  • has a BMI value of 18.5-22.9 kg/m2;
  • there is no history of injury or history of surgery on the lower extremities in the last three months;
  • the individual is in good health.

Exclusion Criteria:

  • absence or refusal to be examined and not cooperative.

Study Plan

This section provides details of the study plan, including how the study is designed and what the study is measuring.

How is the study designed?

Design Details

  • Primary Purpose: Other
  • Allocation: Randomized
  • Interventional Model: Parallel Assignment
  • Masking: Double

Arms and Interventions

Participant Group / Arm
Intervention / Treatment
Experimental: Acupuncture group
Intervention of press tack needle acupuncture
Press tack needle acupuncture using "Seirin Pyonex" sized 0.20x1.2mm
Placebo Comparator: Control group
Intervention of placebo acupuncture
Plesterin

What is the study measuring?

Primary Outcome Measures

Outcome Measure
Measure Description
Time Frame
Leg muscle strength
Time Frame: baseline (Before intervention)
Measurement of leg muscle strength before the intervention, and compared between the two groups
baseline (Before intervention)
Leg muscle strength
Time Frame: 35 minutes after intervention
Measurement of leg muscle strength after the intervention, and compared between the two groups
35 minutes after intervention

Collaborators and Investigators

This is where you will find people and organizations involved with this study.

Study record dates

These dates track the progress of study record and summary results submissions to ClinicalTrials.gov. Study records and reported results are reviewed by the National Library of Medicine (NLM) to make sure they meet specific quality control standards before being posted on the public website.

Study Major Dates

Study Start (Actual)

August 4, 2021

Primary Completion (Actual)

August 15, 2021

Study Completion (Actual)

September 10, 2021

Study Registration Dates

First Submitted

June 23, 2021

First Submitted That Met QC Criteria

July 12, 2021

First Posted (Actual)

July 13, 2021

Study Record Updates

Last Update Posted (Actual)

October 15, 2021

Last Update Submitted That Met QC Criteria

October 7, 2021

Last Verified

October 1, 2021

More Information

Terms related to this study

Other Study ID Numbers

  • 21-05-0541

Plan for Individual participant data (IPD)

Plan to Share Individual Participant Data (IPD)?

NO

Drug and device information, study documents

Studies a U.S. FDA-regulated drug product

No

Studies a U.S. FDA-regulated device product

No

This information was retrieved directly from the website clinicaltrials.gov without any changes. If you have any requests to change, remove or update your study details, please contact register@clinicaltrials.gov. As soon as a change is implemented on clinicaltrials.gov, this will be updated automatically on our website as well.

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