Acute Effect of Foot Reflexology Massage on Heart Rate Variability and Arterial Pulse Waveform

January 26, 2019 updated by: YUNG-SHENG CHEN, University of Taipei

Effects of Foot Reflexology Massage on Heart Rate Variability and Arterial Pulse Waveform After Yo Yo Intermittent Recovery Test and Repeated Sprint Test

Foot reflexology treatment provides acute and chronic effects on cardiovascular and hemodynamic functions. However, no information is available to us in regarding the treatment effect of foot reflexology after exercise. This study investigated the acute effect of foot reflexology treatment on heart rate variability after anaerobic-based and aerobic-based intermittent exercises.

Study Overview

Status

Completed

Intervention / Treatment

Detailed Description

The sympathetic activation and sympathy-vagal balance after repeat sprint performance can be immediately modulated by foot reflexology massage. The acute benefits of foot reflexology intervention on cardiac sympathovagal balance can be considered as exercise recovery strategies in sports.

Study Type

Interventional

Enrollment (Actual)

28

Phase

  • Not Applicable

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 30 years (Adult)

Accepts Healthy Volunteers

No

Genders Eligible for Study

Male

Description

Inclusion Criteria:

  • Undertake football/futsal training at least 3 times a week
  • Age between 18 and 30 years old

Exclusion Criteria:

  • History of severe neuromuscular injury
  • Current lower extremity injury
  • Current neurological diseases

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: Basic Science
  • Allocation: Randomized
  • Interventional Model: Parallel Assignment
  • Masking: None (Open Label)

Arms and Interventions

Participant Group / Arm
Intervention / Treatment
Experimental: Foot reflexology massage group
The duration of intervention was 30 min (15 min massage duration for each leg)
Foot reflexology technique of Father Josef was used as massage intervention
No Intervention: Control group
Rest for 30 min

What is the study measuring?

Primary Outcome Measures

Outcome Measure
Measure Description
Time Frame
Heart rate variability
Time Frame: immediately following intervention phase
15 minutes resting electrocardiographic record at baseline and post-intervention phase
immediately following intervention phase

Secondary Outcome Measures

Outcome Measure
Measure Description
Time Frame
Arterial pulse waveform
Time Frame: immediately following intervention phase
15 minutes resting arterial plethysmographic waveform at baseline and post-intervention phase
immediately following intervention phase

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)

December 22, 2016

Primary Completion (Actual)

June 13, 2017

Study Completion (Actual)

June 13, 2017

Study Registration Dates

First Submitted

January 22, 2019

First Submitted That Met QC Criteria

January 26, 2019

First Posted (Actual)

January 30, 2019

Study Record Updates

Last Update Posted (Actual)

January 30, 2019

Last Update Submitted That Met QC Criteria

January 26, 2019

Last Verified

January 1, 2019

More Information

Terms related to this study

Other Study ID Numbers

  • UT-IRB-2016-017

Plan for Individual participant data (IPD)

Plan to Share Individual Participant Data (IPD)?

No

IPD Plan Description

Individual participant data is protected by IRB application with a minimum of 3 years data storage.

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.

Clinical Trials on Aerobic Exercise

Clinical Trials on Foot reflexology massage

3
Subscribe