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

NCT ID: NCT04133857

Last Updated: 2019-10-21

Study Results

Results pending

The study team has not published outcome measurements, participant flow, or safety data for this trial yet. Check back later for updates.

Basic Information

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Recruitment Status

COMPLETED

Clinical Phase

NA

Total Enrollment

40 participants

Study Classification

INTERVENTIONAL

Study Start Date

2018-01-01

Study Completion Date

2018-02-28

Brief Summary

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

Detailed Description

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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.

Conditions

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Intraocular Pressure

Study Design

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Allocation Method

RANDOMIZED

Intervention Model

CROSSOVER

Primary Study Purpose

TREATMENT

Blinding Strategy

TRIPLE

Participants Investigators Outcome Assessors

Study Groups

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Group A

undergo HIIT first then SSMIT protocol

Group Type ACTIVE_COMPARATOR

aerobic exercise

Intervention Type OTHER

aerobic exercise HIIT : High intensity interval training SSMIT : Steady state moderate intensity training

Group B

undergo SSMIT first then HIIT protocol

Group Type ACTIVE_COMPARATOR

aerobic exercise

Intervention Type OTHER

aerobic exercise HIIT : High intensity interval training SSMIT : Steady state moderate intensity training

Interventions

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aerobic exercise

aerobic exercise HIIT : High intensity interval training SSMIT : Steady state moderate intensity training

Intervention Type OTHER

Eligibility Criteria

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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
Minimum Eligible Age

21 Years

Maximum Eligible Age

60 Years

Eligible Sex

ALL

Accepts Healthy Volunteers

Yes

Sponsors

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University of Malaya

OTHER

Sponsor Role lead

Responsible Party

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Prof Mohd Nahar Azmi Mohamed

associate professor

Responsibility Role PRINCIPAL_INVESTIGATOR

Locations

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University Malaya

Kuala Lumpur, Wilayah Perseketuan, Malaysia

Site Status

Countries

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Malaysia

Provided Documents

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Document Type: Study Protocol and Statistical Analysis Plan

View Document

Other Identifiers

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20171031-5738

Identifier Type: -

Identifier Source: org_study_id

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