NCT03563430

Brief Summary

The aim of this study is to compare these three different recovery methods following a single bout high-intensity interval exercise program with each other in terms of blood lactate clearance, muscle flexibility, muscle strength and endurance.

Trial Health

87
On Track

Trial Health Score

Automated assessment based on enrollment pace, timeline, and geographic reach

Enrollment
45

participants targeted

Target at P25-P50 for not_applicable

Timeline
Completed

Started Sep 2017

Shorter than P25 for not_applicable

Geographic Reach
1 country

1 active site

Status
completed

Health score is calculated from publicly available data and should be used for screening purposes only.

Trial Relationships

Click on a node to explore related trials.

Study Timeline

Key milestones and dates

Study Start

First participant enrolled

September 25, 2017

Completed
8 months until next milestone

First Submitted

Initial submission to the registry

May 28, 2018

Completed
23 days until next milestone

First Posted

Study publicly available on registry

June 20, 2018

Completed
11 days until next milestone

Primary Completion

Last participant's last visit for primary outcome

July 1, 2018

Completed
Same day until next milestone

Study Completion

Last participant's last visit for all outcomes

July 1, 2018

Completed
Last Updated

September 5, 2018

Status Verified

September 1, 2018

Enrollment Period

9 months

First QC Date

May 28, 2018

Last Update Submit

September 4, 2018

Conditions

Keywords

foam rollerelectrical stimulationlow intensity aerobic traininglactate removal

Outcome Measures

Primary Outcomes (1)

  • Blood Lactate change

    blood lactate concentration measurement

    change from baseline and 20. minutes of recovery

Secondary Outcomes (3)

  • Quadriceps and Hamstring Muscle Strength

    baseline and 1. hour

  • Squat Endurance Test

    baseline and 1. hour

  • sit and reach test

    baseline and 1. hour

Study Arms (3)

Active Recovery Group

EXPERIMENTAL

Participants in this group will exercise for 15 minutes, for a range of 65 to 70% of the maximum heart rate.

Other: Active Recovery Group

Self-Massage with Foam Roller Group

EXPERIMENTAL

This group will perform 15 minutes self-massage with foam roller following the exercise session.

Other: Self-Massage with Foam Roller Group

Neuromuscular Electrical Stimulation

EXPERIMENTAL

Participants of this group will be applied electrical stimulation on quadriceps femoris and hamstring muscles for 15 minutes while they are comfortable lying position.

Other: Neuromuscular Electrical Stimulation

Interventions

Participants in this group will exercise for 15 minutes, for a range of 65 to 70% of the maximum heart rate as a recovery method following a single bout high-intensity interval exercise program

Active Recovery Group

This group will perform 15 minutes self-massage with foam roller following the exercise session as a recovery method following a single bout high-intensity interval exercise program.

Self-Massage with Foam Roller Group

Participants of this group will be applied electrical stimulation on quadriceps femoris and hamstring muscles for 15 minutes while they are comfortable lying position as a recovery method following a single bout high-intensity interval exercise program.

Neuromuscular Electrical Stimulation

Eligibility Criteria

Age20 Years - 25 Years
Sexall
Healthy VolunteersYes
Age GroupsAdult (18-64)

You may qualify if:

  • Young, healthy adults aged 20-25 years.

You may not qualify if:

  • Clinical diagnosis of a cardiovascular disease.
  • Clinical diagnosis of a metabolic disorder, orthopedic or neurological disease that would interfere with an exercise program,
  • Clinical diagnosis of hemophili,
  • Clinical diagnosis of thrombophlebitis or deep vein trombosis,
  • Clinical diagnosis of peripheral arterial disease,
  • Clinical diagnosis of venous insufficiency,
  • Clinical diagnosis of anemia,
  • Pregnancy.

Contact the study team to confirm eligibility.

Sponsors & Collaborators

Study Sites (1)

Biruni University

Istanbul, 34010, Turkey (Türkiye)

Location

Study Officials

  • Buket AKINCI, PhD

    Biruni University

    STUDY CHAIR

Study Design

Study Type
interventional
Phase
not applicable
Allocation
RANDOMIZED
Masking
TRIPLE
Who Masked
PARTICIPANT, INVESTIGATOR, OUTCOMES ASSESSOR
Purpose
BASIC SCIENCE
Intervention Model
PARALLEL
Model Details: neuromuscular electrical stimulation, low intensity aerobic exercise, self massage with foam roller methods
Sponsor Type
OTHER
Responsible Party
PRINCIPAL INVESTIGATOR
PI Title
Principal Investigator, Head of Physiotherapy and Rehabilitation Department

Study Record Dates

First Submitted

May 28, 2018

First Posted

June 20, 2018

Study Start

September 25, 2017

Primary Completion

July 1, 2018

Study Completion

July 1, 2018

Last Updated

September 5, 2018

Record last verified: 2018-09

Locations