- ICH GCP
- US Clinical Trials Registry
- Clinical Trial NCT04133857
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
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.
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)
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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