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The Effect of Transcutaneous Electrical Nerve Stimulation on People With Muscle Fatigue Due to Training, Sports

O

Omron Healthcare

Status

Unknown

Conditions

Muscle Fatigue

Treatments

Device: Sham
Device: electrical stimulation

Study type

Interventional

Funder types

Other
Industry

Identifiers

NCT04082156
HI794-0014

Details and patient eligibility

About

The objective is to assess if TENS will improve the muscle recovery rate from post-exercise fatigue.

Enrollment

30 estimated patients

Sex

All

Ages

18 to 45 years old

Volunteers

Accepts Healthy Volunteers

Inclusion criteria

  • No phobia of electrical stimulation
  • No pain or anti-inflammatory medication will be taken during study
  • English speaking

Exclusion criteria

  • Pregnancy
  • Diabetes Mellitus
  • Neuropathy
  • Smoker
  • Uncontrolled Hypertension
  • Past surgery in the region to be treated by TENS or had received an intra-articular corticosteroid or hyaluronic acid injection within 6 months prior to enrollment
  • Rhumatoid Arthritis (RA) in the area to be treated by TENS
  • Allergic to tape/electrodes
  • Dementia
  • History of knee joint replacement or tibial osteotomy
  • Undergoing physical therapy
  • Any major joint pain (e.g., back, hip, or ankle) that could limit functional ability
  • Contraindications to TENS such as having a pacemakers, dermatological conditions, and abnormal sensation of the lower extremity.

Trial design

Primary purpose

Treatment

Allocation

Randomized

Interventional model

Crossover Assignment

Masking

Single Blind

30 participants in 2 patient groups

Active TENS
Active Comparator group
Treatment:
Device: electrical stimulation
Sham TENS
Sham Comparator group
Treatment:
Device: Sham

Trial contacts and locations

1

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Central trial contact

Daryl Lawson, DSc

Data sourced from clinicaltrials.gov

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