Efficacy of Plyometric Training Supplementation With NMES on Quadriceps Strength and Functional Performance.

Sponsor
Majmaah University (Other)
Overall Status
Completed
CT.gov ID
NCT05056792
Collaborator
(none)
60
1
2
6.9
8.7

Study Details

Study Description

Brief Summary

This study aims to investigate the influence of an eight-week Neuromuscular Electrical stimulation (NMES) add-on with a training program on muscular strength, sprint, and functional performance in collegiate football players.

Condition or Disease Intervention/Treatment Phase
  • Other: NMES strength training for 8 week
N/A

Detailed Description

Sixty collegiate football players aged 18-25 years were recruited, at the university campus. All of which were randomly divided into two experimental and control groups that participated in training for six weeks on alternate days (i.e., three sessions per week), and one control group (n=30) did not train. The control group was instructed to maintain regular activities and avoid any strenuous physical activity during the study.

Under the Declaration of Helsinki, participants were informed about the study's possible risks and benefits, and all participants have signed informed consent before participation in the study. The ethical sub-committee of the College of applied medical science, Majmaah, Saudi Arabia approved this study (Ethics Number: MUREC-Dec. 15/COM-2020 / 13-2).

Study Design

Study Type:
Interventional
Actual Enrollment :
60 participants
Allocation:
Randomized
Intervention Model:
Parallel Assignment
Intervention Model Description:
Randomized controlled trialRandomized controlled trial
Masking:
Double (Participant, Care Provider)
Masking Description:
Randomized
Primary Purpose:
Prevention
Official Title:
Efficacy of Plyometric Training Supplementation With Neuromuscular Electrical Stimulation on Quadriceps Strength and Functional Performance in Collegiate Male Football Players: A Randomized Control Study
Actual Study Start Date :
Dec 30, 2020
Actual Primary Completion Date :
Jun 30, 2021
Actual Study Completion Date :
Jul 28, 2021

Arms and Interventions

Arm Intervention/Treatment
Experimental: Participants in this group will receive NMES guided strength training.

NMES guided strength training of the quadriceps femoris muscle for 8 weeks.

Other: NMES strength training for 8 week
Plyometric training for 8 week
Other Names:
  • plyometric training
  • Sham Comparator: Participants in this group will receive Sham NMES.

    Participants in this group will receive Sham NMES guided strength training of the quadriceps femoris muscle for 8 weeks.

    Other: NMES strength training for 8 week
    Plyometric training for 8 week
    Other Names:
  • plyometric training
  • Outcome Measures

    Primary Outcome Measures

    1. Maximal Voluntary Isometric Contraction Strength (STN) [After 8 weeks of intervention]

      Pretest and post intervention strength measure.

    2. Sprint Test (ST) [After 8 weeks of intervention]

      Pretest and post intervention sprint measure.

    3. Single-Leg Triple Hop Test (SLTH) [After 8 weeks of intervention]

      Pretest and post intervention single-leg triple hop measure.

    Eligibility Criteria

    Criteria

    Ages Eligible for Study:
    18 Years to 25 Years
    Sexes Eligible for Study:
    Male
    Accepts Healthy Volunteers:
    Yes
    Inclusion Criteria:

    • Young players aged between 18 and 25 years required frequent sprinting

    Exclusion Criteria:
    • Current injury to the lower limb.

    • Surgery affecting lower limb function.

    • Any cardio-respiratory diseases.

    • Impairments of the spine or lower extremities.

    Contacts and Locations

    Locations

    Site City State Country Postal Code
    1 Physiotherapy and Rehabilitation center Al Majma'ah Riyadh Saudi Arabia 11952

    Sponsors and Collaborators

    • Majmaah University

    Investigators

    • Principal Investigator: Shahnaz Hasan, PhD, Majmaah University

    Study Documents (Full-Text)

    None provided.

    More Information

    Publications

    None provided.
    Responsible Party:
    Shahnaz Hasan, PhD, Associate Professor, Majmaah University
    ClinicalTrials.gov Identifier:
    NCT05056792
    Other Study ID Numbers:
    • DSR Majmaah University
    First Posted:
    Sep 27, 2021
    Last Update Posted:
    Sep 27, 2021
    Last Verified:
    Sep 1, 2021
    Individual Participant Data (IPD) Sharing Statement:
    No
    Plan to Share IPD:
    No
    Studies a U.S. FDA-regulated Drug Product:
    No
    Studies a U.S. FDA-regulated Device Product:
    No
    Keywords provided by Shahnaz Hasan, PhD, Associate Professor, Majmaah University

    Study Results

    No Results Posted as of Sep 27, 2021