CClinicalTrials.gg
CompletedNCT03448120Updated Mar 2, 2022

Acupuncture and Dry Needling in Peripheral Acute Fatigue Reduction

An interventional study of Acupuncture and Dry needling in Sedentary Lifestyle and Males, sponsored by Universidade Federal de Pernambuco. Completed at 1 site in Brazil. Open to male participants aged 18 Years to 40 Years, including healthy volunteers. Per ClinicalTrials.gov, last updated 2022-03-02.

Sponsored by Universidade Federal de Pernambuco · Not applicable, Interventional, and Treatment

Phase
Not applicable
Study type
Interventional
Enrollment
45
Allocation
Randomized
Ages
18 Years to 40 Years
Sex
Male
01

Study summary

Introduction: Neuromuscular fatigue is defined when the muscle becomes incapable of generating muscle power or strength after exercise or long repetitive activities. As well as, the inability to maintain optimum performance and generate maximum voluntary contractions during a physical exercise. When performing physical activity, the body's metabolic response increases proportionally to exercise to satisfy the demands of the human physiological. Part of the energy accumulated during exercise is lost to the environment in the form of heat and another part is maintained internally through the physiological control for thermoregulation. In addition, the muscle generates an electric signal important to determine its status regarding power and fatigue.

Objective: To investigate the reduction of acute peripheral fatigue induced by isometric contractions from acupuncture and dry needling techniques, compared to absolute rest.

Methods: This is a cross-sectional study and experimental study, with descriptive, analytical and quantitative approach. It follows the Consolidated Standards of Reporting Trials (CONSORT) guidelines. The volunteers will be gathered according to the eligibility criteria, and randomly divided in 3 groups: the control group (G1), the volunteers who will remain in prolonged rest; the acupuncture group (G2), in which volunteers will receive six needles in six acupoints in the non-dominant upper limb and the dry needling group (G3), in which the volunteers will receive application of six needles arranged in the non-dominant biceps brachialis.

02

Conditions studied

  • Sedentary Lifestyle
  • Males

Browse trials for

Keywords

  • Muscle fatigue
  • Thermography
  • Acupuncture
  • Dry needling
03

Who can participate

Ages eligible
18 Years to 40 Years
Sexes eligible
Male
Accepts healthy volunteers
Yes

Inclusion criteria

  • Male individuals, aged between 18 and 40 years and who are not practicing regular physical activity (sedentary lifestyle).

Exclusion criteria

Exclusion Criteria:

  • Are using food supplementation;
  • Have joint or bone lesions on the limb to be studied;
  • Have problems of metabolic order;
  • Use of hormone therapy;
  • Have had caffeine in the two hours before the study;
  • Have ulceration or wounds in the electrode application region for electromyography;
  • Show absence of myofascial trigger points in areas of dry needling technique;
  • Body Mass Index below normal values or higher than overweight.
04

Study design

Phase
Not applicable
Primary purpose
Treatment
Allocation
Randomized
Intervention model
Factorial assignment
Masking
Single (Care provider)
Enrollment
45 participants (actual)

Study arms

  • No intervention
    Control Group

    The volunteers who will remain in prolonged rest (10 minutes for homeostasis plus 30 minutes of no intervention).

  • Experimental
    Acupuncture Group

    The volunteers will receive six needles in six acupoints in the non-dominant upper limb for 30 minutes.

    Procedure: Acupuncture

  • Experimental
    Dry needling Group

    The volunteers will receive application of six needles arranged in the non-dominant biceps brachialis for 30 minutes.

    Procedure: Dry needling

Interventions

  • ProcedureAcupuncture

    Six needled will be inserted in six already defined acupoints along the non-dominant upper limb for a period of 30 minutes.

  • ProcedureDry needling

    Six needles will be inserted in six predefined points along the volunteers non-dominant biceps brachialis for 30 minutes.

05

What researchers measure

Primary outcomes

  1. Perception of muscle fatigue

    Fatigue perception measured by Visual Analog Scale for fatigue assessment, graduated from 0,00 to 10,0 centimeters, being 0,00 no fatigue and 10,0 maximum fatigue.

    Time frame: 60 minutes

  2. Muscle temperature

    Infrared thermographic Imaging analysis of acute peripheral muscle fatigue.

    Time frame: 60 minutes

  3. Muscle fatigue

    Electromyographic activity (in microvolts) of the biceps brachii muscle to assess muscle fatigue through the median frequency (MF).

    Time frame: 60 minutes

Other outcomes

  1. Contraction time

    The time of intermittent isometric contractions was delimited by the number of valid contractions during each exercise

    Time frame: 60 minutes

06

Study locations

1 site
  • Laboratory of Kinesiotherapy and Manual Therapeutic Resources, Department of Physical Therapy, Federal University of Pernambuco (UFPE)
    Recife, Pernambuco 50670-901, Brazil
07

References and documents

Publications

  • Antonino GB, Paula de Lima Ferreira A, Nepomuceno Montenegro EJ, Galvao de Moura Filho A, Freire da Silva AF, de Araujo MDGR. Acupuncture and Dry Needling in the Reduction of Peripheral Acute Fatigue Induced in the Biceps Braquii: Protocol for a Single-blinded Randomized Controlled Clinical Trial. J Acupunct Meridian Stud. 2020 Oct;13(5):163-166. doi: 10.1016/j.jams.2020.08.001. Epub 2020 Sep 1. PubMed 32889135 ↗
08

Registry details

Key details

Study ID
NCT03448120
Lead sponsor
Universidade Federal de Pernambuco
Responsible party
Maria das Graças Rodrigues de Araújo (Professor of the Physiotherapy Department, Universidade Federal de Pernambuco) — Principal investigator
First posted
Feb 27, 2018
Start date
Feb 26, 2018
Primary completion
Nov 16, 2018
Completion
Dec 21, 2018
Last update
Mar 2, 2022

Oversight

Data monitoring committee
No
FDA-regulated drug
No
FDA-regulated device
No
View the source record on ClinicalTrials.gov ↗

Not currently enrolling

This study is completed, as verified in Feb 2022. You cannot join it, but the record below documents what was studied.

Follow this study

Get an email when the registry record changes — status, dates, results — or when someone posts here.

Sign in to follow

Discussion

Questions and observations about this study, from anyone following it. Not medical advice, and not a channel to the study team — their contact details are on the registry record.

Sign in to join the discussion. Reading takes no account; posting does. You choose a display name, and a pseudonym is the default.

Nothing here yet. If you are running this trial, taking part in it, or weighing whether to, this is the place to say so.

Start the discussion