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Individuals With Eye Refraction DefectsNCT05999552

The Effect of Eye Exercises in Individuals With Eye Refractive Defects

A study testing Eye exercises in people with Individuals With Eye Refraction Defects, run by Hacettepe University at 1 site in Turkey (Türkiye).

Completed

Finished. The study has ended and is not enrolling. Results may be posted on the official record.

Official record
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Trial summary

According to the World Health Organization's statement published in 2014, 43% of visual impairment is overhauled by uncorrected refractive errors. The change of body and angle of light waves while undergoing changes in the environment due to the temperature difference between the environments is called refraction. Read more about this study

Who is it for?
Ages 18 to 65 yearsHealthy volunteers can take part
Conditions the study is for
Individuals With Eye Refraction Defects
What is being tested?
Eye exercises
Could I receive a placebo?
No, everyone receives an active treatment
How many people
40 participants
Where
1 siteTurkey (Türkiye)
Study dates
5 Sep 2023to 30 Jun 2024
Phase
Interventional
Are there results?
None posted in the registry

Key requirements

Who can take part, as listed by the sponsor. Only the study team can confirm whether you are eligible, so take this list to your doctor.

  • Ages 18 to 65 years
  • All sexes
  • Healthy volunteers accepted
  • Adult, Older adult

Who may be able to join

  • be between the ages of 18-65, Having any refractive or visual impairment (myopia, hyperopia, astigmatism) by an ophthalmologist, not have other eye problems in addition to these vision defects, to score at least 24 on the Standardized Mini Mental Test.

Who cannot join

  • having undergone any eye surgery (including laser operations), have a prosthetic eye have congenital vision loss, have any disease that will affect the eyesight. Individuals meeting these criteria will not be included in the study.

Trial locations and contacts

1 site in 1 country.

Turkey (Türkiye)1 site
  • Van bölge hastanesi eğitim ve araştırma hastanesi

    Van

Other trials in Turkey (Türkiye)

About this study

Official title: The Effect of Eye Exercises Applied on Individuals With Eye Refractive Defects on Visual Function and Quality of Life

According to the World Health Organization's statement published in 2014, 43% of visual impairment is overhauled by uncorrected refractive errors. The change of body and angle of light waves while undergoing changes in the environment due to the temperature difference between the environments is called refraction. The refractive errors found in the eye can be discovered as myopia, astigmatism, hyperopia, and presbyopia. As there are different prevalence methods in eye refractive errors in various publications. According to many studies in the literature, eye exercises in many conditions such as convergence collapse, accommodation dysfunction, movement center of the eye, digital eye strain and dry eye are curative and therapeutic without any control. With eye exercises, blood is applied to the ocular region, the humor is stimulated, the tension of the extraocular muscles is reduced, the coordination between the eye muscles is increased, the eye fatigue and stress are reduced. Depending on the effects of these effects, positive changes are seen on vision tests. Although there is a different view in the literature that includes these eye exercises and their benefits, it has been found to be insufficient in current studies. More work needs to be done in this area so that these results can be stated better and more clearly. With this study, investigators aim to shed light on what can be done in this field by filling these residents in the literature and to examine the visual function and quality of life of eye exercises.

Being tested
Eye exercises
Keywords
Ocular Refraction, Eye, Exercise, Life Quality, Ocular vision
Medical subject headings
Motor Activity

What participants receive

What participants receive. In a randomised study each person is assigned to one group by chance.

  • Eye exercisesOther

    The treatment will be applied in three sessions a week for eight weeks and each session will be approximately 20 minutes. Individuals will do each exercise shown at home as a home program on other days (days when the physiotherapist does not perform the exercise by video call).

Study groups in NCT05999552
Study groupRoleWhat they receive
Control GroupNo interventionany exercise program will not be applied and will only be followed.
Experimental GroupExperimentaleye exercise program will be applied.
Receives: Other: Eye exercises

What is being measured

The primary outcome is the main question the study is designed to answer.

  1. Nottingham Health profile

    This questionnaire assesses the perception of health-related quality of life. The total score is between 0-600. A high score is an indication of a bad outcome.

    Measured: baseline, after 8 weeks

  2. National Institute of Ophthalmology Visual Function Scale

    Used to measure vision-related quality of life in patients with chronic eye disease. Overall scores ranged from 0 to 100, with higher scores indicating better quality of life.

    Measured: baseline, after 8 weeks

  3. Standardized Mini-Mental Test

    It is a scale that determines the cognitive level of the participants. It consists of eleven questions and is evaluated over 30 points. 24-30 points are normal, 18-23 points mild dementia, 10-17 points dementia, 10 points and below are compatible with severe dementia.

    Measured: baseline

Timeline

From the start of the study to its completion; the mark is today. Estimated dates are the sponsor’s plan.

  1. First posted21 Aug 2023
  2. Study start5 Sep 2023
  3. Primary completion15 Dec 2023
  4. Study completion30 Jun 2024

Resources

More details

For doctors and researchers: how the study is designed, who runs it, and its registry IDs.

Study design
Study type
Interventional
Phase
Phase N/A
Primary purpose
Treatment
Allocation
Randomised
Intervention model
Parallel groups
Masking
Single blind
Who is masked
Participant
Enrolment
40 participants (actual)
IDs, dates and publications
ClinicalTrials.gov ID
NCT05999552
Sponsor's protocol ID
Eye Exercises
Status last verified
Sep 2025
First submitted
29 Jul 2023
Last updated
2 Oct 2025
Results posted
No
Data monitoring committee
No
FDA-regulated drug
No
FDA-regulated device
No
Individual data sharing
Yes

Publications

  • Blindness and visual impairment. [Internet]. World Health Organization, 2014.

  • Convergence Insufficiency Treatment Trial (CITT) Study Group. The convergence insufficiency treatment trial: design, methods, and baseline data. Ophthalmic Epidemiol. 2008 Jan-Feb;15(1):24-36. doi: 10.1080/09286580701772037.

    PubMed 18300086
  • Horwood A, Toor S. Clinical test responses to different orthoptic exercise regimes in typical young adults. Ophthalmic Physiol Opt. 2014 Mar;34(2):250-62. doi: 10.1111/opo.12109. Epub 2014 Jan 29.

    PubMed 24471739
  • Cacho Martinez P, Garcia Munoz A, Ruiz-Cantero MT. Treatment of accommodative and nonstrabismic binocular dysfunctions: a systematic review. Optometry. 2009 Dec;80(12):702-16. doi: 10.1016/j.optm.2009.06.011.

    PubMed 19932444
  • Minoonejad H, Barati AH, Naderifar H, Heidari B, Kazemi AS, Lashay A. Effect of four weeks of ocular-motor exercises on dynamic visual acuity and stability limit of female basketball players. Gait Posture. 2019 Sep;73:286-290. doi: 10.1016/j.gaitpost.2019.06.022. Epub 2019 Jul 16.

    PubMed 31398634
  • Morimoto H, Asai Y, Johnson EG, Lohman EB, Khoo K, Mizutani Y, Mizutani T. Effect of oculo-motor and gaze stability exercises on postural stability and dynamic visual acuity in healthy young adults. Gait Posture. 2011 Apr;33(4):600-3. doi: 10.1016/j.gaitpost.2011.01.016. Epub 2011 Feb 19.

    PubMed 21334899

Questions about this trial

What is this clinical trial studying?

A study testing Eye exercises in people with Individuals With Eye Refraction Defects, run by Hacettepe University at 1 site in Turkey (Türkiye).

The full registered description is in the About this study section and the official record.

Who may be eligible to take part?

The sponsor lists 1 inclusion and 1 exclusion criteria. Eligibility is decided by the study team after screening, so read the full criteria and contact a listed site.

Is this clinical trial currently recruiting?

The record says: finished, as of the sponsor's last update on 2 Oct 2025. Status can change between updates, so confirm with the study contact before making plans.

Where is the study taking place?

The record lists 1 site in Turkey (Türkiye). Whether a site is taking part right now should be confirmed with that site. See every site.

What are the possible benefits and risks?

They depend on the study and the treatment, and no study can promise a benefit. The study team explains the known risks during informed consent, before anyone joins; the record itself does not list them.

Are results available for this study?

The study is completed, but results are not available in the source record. That does not mean the treatment did or did not work.

How can a doctor refer a patient or contact the research team?

The record lists no contact. The official record names the sponsor, who can be asked directly. AzTrials does not enrol participants or take referrals.

What does the primary outcome measure?

Nottingham Health profile (time frame: baseline, after 8 weeks). The study lists 3 primary outcomes in all. It is what the study was designed to measure, not a finding.

Where can I read the original study information?

On the ClinicalTrials.gov record for NCT05999552, which also lists 6 linked publications.

Does a listing mean the treatment is approved or proven to work?

No. A listing means the study is registered. It does not show that the treatment is safe, works, or is approved by a regulator.

How often is this information updated?

AzTrials copies changed records from ClinicalTrials.gov every night and reloads the whole registry every week. The sponsor last updated this record on 2 Oct 2025.

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