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Gac Fruit Oil Supplementation for Visual Health and Sleep Quality

Study on Visual Health Promotion and Carotenoids From Momordica Cochinchinensis

Status
Completed
Phases
Unknown
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT07623070
Enrollment
50
Registered
2026-06-03
Start date
2022-09-01
Completion date
2023-07-16
Last updated
2026-06-03

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Sleep Disturbance, Visual Health

Keywords

Gac fruit oil, Momordica cochinchinensis, Sleep quality, Visual health, Depressive symptoms

Brief summary

This study evaluated the effects of gac fruit oil supplementation on visual health, sleep quality, depressive symptoms, cognitive function, and brain imaging parameters in adults with sleep disturbance. Participants aged 40 to 65 years were recruited and received gac fruit oil capsules for 30 days. The supplementation protocol consisted of two capsules in the morning and two capsules in the evening each day. Assessments were performed before and after the intervention, including macular pigment measurement, ocular surface disease evaluation, tear film analysis, contrast sensitivity testing, accommodative microfluctuation analysis, optical coherence tomography, the Pittsburgh Sleep Quality Index, a depression scale, the Mini-Mental State Examination, and brain magnetic resonance imaging. The study aimed to explore whether 30 days of gac fruit oil supplementation was associated with changes in visual function, sleep quality, mood-related measures, cognitive function, and brain imaging findings.

Interventions

DIETARY_SUPPLEMENTGac Fruit Oil Capsules

Participants took gac fruit oil capsules orally for 30 days. The supplementation protocol consisted of two capsules in the morning and two capsules in the evening each day, for a total of four capsules per day.

Sponsors

Yuanpei University of Medical Technology
Lead SponsorOTHER

Study design

Allocation
NA
Intervention model
SINGLE_GROUP
Primary purpose
SUPPORTIVE_CARE
Masking
NONE

Intervention model description

All participants received the same intervention: gac fruit oil capsules for 30 days. Outcomes were assessed before and after the intervention.

Eligibility

Sex/Gender
ALL
Age
40 Years to 65 Years
Healthy volunteers
No

Inclusion criteria

* Adults aged 40 to 65 years. * Participants with sleep disturbance. * Participants who were willing to participate in the study and provide written informed consent.

Exclusion criteria

* History of ocular surgery. * Cataract. * Glaucoma. * Current supplementation intended to increase macular pigment level. * Pregnancy. * Severe illness. * Use of medications that may affect or stimulate sleep. * Use of medications that promote sleep. * Unable to undergo magnetic resonance imaging, including but not limited to individuals with a pacemaker, artificial heart valve, metal aneurysm clip, metallic tracheostomy tube, possible metallic fragments in the orbit, cochlear implant, implanted electrodes, neurostimulator, implanted drug infusion device, hemostatic clips, vascular stents, claustrophobia, previous brain surgery, or history of traumatic brain injury with implanted metal materials. * Participants who experienced discomfort during the study or wished to withdraw could discontinue participation at any time without providing a reason.

Design outcomes

Primary

MeasureTime frameDescription
Change in Sleep QualityBaseline and 30 daysSleep quality was assessed using the Pittsburgh Sleep Quality Index before and after 30 days of gac fruit oil supplementation.

Secondary

MeasureTime frameDescription
Change in Depressive SymptomsBaseline and 30 daysDepressive symptoms were assessed using a depression scale before and after 30 days of gac fruit oil supplementation.
Change in Macular Pigment LevelBaseline and 30 daysMacular pigment level was assessed using a macular pigment screener before and after 30 days of gac fruit oil supplementation.
Change in Ocular Surface Disease SymptomsBaseline and 30 daysOcular surface disease symptoms were assessed using the Ocular Surface Disease Index before and after 30 days of gac fruit oil supplementation.
Change in Tear Film ParametersBaseline and 30 daysTear film parameters were assessed using a non-contact ocular surface analyzer before and after 30 days of gac fruit oil supplementation.
Change in Contrast SensitivityBaseline and 30 daysContrast sensitivity was assessed using the CVS-1000 contrast sensitivity test before and after 30 days of gac fruit oil supplementation.
Change in Accommodative MicrofluctuationBaseline and 30 daysAccommodative microfluctuation was assessed using an accommodative microfluctuation analyzer before and after 30 days of gac fruit oil supplementation.
Change in Retinal StructureBaseline and 30 daysRetinal structure was assessed using optical coherence tomography before and after 30 days of gac fruit oil supplementation.
Change in Cognitive FunctionBaseline and 30 daysCognitive function was assessed using the Mini-Mental State Examination before and after 30 days of gac fruit oil supplementation.
Change in Brain Magnetic Resonance Imaging ParametersBaseline and 30 daysBrain magnetic resonance imaging parameters were assessed before and after 30 days of gac fruit oil supplementation.

Countries

Taiwan

Contacts

PRINCIPAL_INVESTIGATORChao-Kai Chang

Yuanpei University of Medical Technology

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Jun 4, 2026