- ICH GCP
- US Clinical Trials Registry
- Clinical Trial NCT03821805
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
Conditions
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.
Sponsor
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.
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