Acute Effects of HIIT and SSMIT on Intraocular Pressure Among Sedentary Individuals

October 17, 2019 updated by: Prof Mohd Nahar Azmi Mohamed, University of Malaya

Acute Effects of High Intensity Interval Training (HIIT) and Steady State Moderate Intensity Training (SSMIT) on Intraocular Pressure Among Sedentary Individuals

Purpose to study the acute effects of both forms of aerobic exercise (HIIT and SSMIT) on intraocular pressure among healthy sedentary individuals

Study Overview

Status

Completed

Intervention / Treatment

Detailed Description

40 participants were recruited and divided into 2 groups. Each group performed 2 exercise protocols with a 4 day washout period between them.

The intraocular pressure was measured before the exercise and after the exercise in 5 minute periods up until 30 minutes post exercise.

The intraocular pressure was measured using a handheld rebound tonometer.

Study Type

Interventional

Enrollment (Actual)

40

Phase

  • Not Applicable

Contacts and Locations

This section provides the contact details for those conducting the study, and information on where this study is being conducted.

Study Locations

    • Wilayah Perseketuan
      • Kuala Lumpur, Wilayah Perseketuan, Malaysia, 59100
        • University Malaya

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

21 years to 60 years (Adult)

Accepts Healthy Volunteers

No

Genders Eligible for Study

All

Description

Inclusion Criteria:

  • all University hospital staff

Exclusion Criteria:

  • previous ocular trauma
  • surgery in the eligible eye
  • known case of glaucoma or glaucoma suspect (IOP > 21mmHg)
  • history of glaucoma laser procedure/surgery within 6 months in eligible eye
  • unable to undergo IOP measurements
  • undiagnosed visual condition
  • any uncontrolled medical condition such as end stage renal failure, uncontrolled diabetes and uncontrolled hypertension

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: Treatment
  • Allocation: Randomized
  • Interventional Model: Crossover Assignment
  • Masking: Triple

Arms and Interventions

Participant Group / Arm
Intervention / Treatment
Active Comparator: Group A
undergo HIIT first then SSMIT protocol
aerobic exercise HIIT : High intensity interval training SSMIT : Steady state moderate intensity training
Active Comparator: Group B
undergo SSMIT first then HIIT protocol
aerobic exercise HIIT : High intensity interval training SSMIT : Steady state moderate intensity training

What is the study measuring?

Primary Outcome Measures

Outcome Measure
Measure Description
Time Frame
Changes in intraocular pressure
Time Frame: 30 minutes
changes in intraocular pressure before and after exervcise
30 minutes

Secondary Outcome Measures

Outcome Measure
Measure Description
Time Frame
compare which form of exercise (HIIT & SSMIT) is superior in reducing intraocular pressure
Time Frame: 30 days
difference in intraocular pressure reduction observed between each exercise protocol
30 days

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)

January 1, 2018

Primary Completion (Actual)

January 31, 2018

Study Completion (Actual)

February 28, 2018

Study Registration Dates

First Submitted

October 11, 2019

First Submitted That Met QC Criteria

October 17, 2019

First Posted (Actual)

October 21, 2019

Study Record Updates

Last Update Posted (Actual)

October 21, 2019

Last Update Submitted That Met QC Criteria

October 17, 2019

Last Verified

October 1, 2019

More Information

Terms related to this study

Other Study ID Numbers

  • 20171031-5738

Plan for Individual participant data (IPD)

Plan to Share Individual Participant Data (IPD)?

No

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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