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NCT02972749 Clinical Trial

Modifiable Factors and Glaucoma - RCT

Intraocular Pressure Clinical Trial

Official title:
Modifiable Factors in the Management of Glaucoma - a Randomized Controlled Trial

Clinical Trial Details — Status: Completed

Administrative data
NCT number NCT02972749
Other study ID # 0127-16-WOMC
Secondary ID
Status Completed
Phase N/A
First received November 20, 2016
Last updated December 31, 2017
Start date November 2016
Est. completion date December 2017

Study information
Verified date December 2017
Source Wolfson Medical Center
Contact n/a
Is FDA regulated No
Health authority
Study type Interventional

Clinical Trial Summary

There is growing awareness that environmental factors, behaviors and diet are intimately related to patient health and may play a role in the pathogenesis and progression of glaucoma. Evidence from recent years has shown that some behaviors and environmental factors can affect the intraocular pressure, the primary risk factor for glaucoma. This study aims to investigate whether simple and common lifestyle inteventions such as sleeping with a head elevation, a high fiber diet, moderate aerobic exercise and moderation in caffeine intake could affect intraocular pressure and other outcomes.

Recruitment information / eligibility
Status Completed
Enrollment 22
Est. completion date December 2017
Est. primary completion date December 2017
Accepts healthy volunteers No
Gender All
Age group 18 Years and older
Eligibility Inclusion Criteria:

- Patients with glaucoma.

Exclusion Criteria:

- Not able to attend follow-up

- Contraindication for treatment or follow-up

Study Design

Related Conditions & MeSH terms

Intervention

Behavioral:
• Intervention
Recommendations for lifestyle changes which have shown to reduce IOP. recommendations include: Moderate aerobic exercise, High fiber diet, sleeping with a head elevation and moderating caffeine intake. while continuing prescribed medical therapy.

Locations
Country Name City State
Israel The E.Wolfson Medical Center Holon

Sponsors (1)
Lead Sponsor Collaborator
Wolfson Medical Center

Country where clinical trial is conducted

Israel, 

Outcome
Type Measure Description Time frame Safety issue
Primary Intraocular pressure Following 1 month of treatment
Secondary Illness perception questionnaire results Following 1 month of treatment
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