Alternate Nostril Breathing Training in Geriatrics With Glaucoma and High Blood Pressure

October 30, 2022 updated by: Ali Mohamed Ali ismail, Cairo University

Ocular Hypertension Response to Alternate Nostril Breathing Training in Geriatrics With Glaucoma and High Blood Pressure

Hypertension, particularly if poorly controlled, appears related to an increased risk of open angle glaucoma, (the high tension type of glaucoma is characterized as optic nerve degeneration with ocular hypertension). so this study will search response of glaucoma to breathing exercise

Study Overview

Status

Recruiting

Intervention / Treatment

Detailed Description

Hypertension, particularly if poorly controlled, appears related to an increased risk of open angle glaucoma, (the high tension type of glaucoma is characterized as optic nerve degeneration with ocular hypertension). With a random assignment, sixty hypertensive geriatric with high tension type primary open angle glaucoma will be assigned to breathing exercise (alternate nostril breathing) group (n=30 geriatrics) or waiting list geriatrics. the daily breathing exercise will be performed by the geriatrics in evening (for half an hour) and morning (for half an hour).

Study Type

Interventional

Enrollment (Anticipated)

60

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 Contact

Study Contact Backup

Study Locations

    • Dokki
      • Giza, Dokki, Egypt
        • Recruiting
        • Faculty of Physical Therapy Cairo University

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

61 years to 71 years (Older Adult)

Accepts Healthy Volunteers

No

Genders Eligible for Study

All

Description

Inclusion Criteria:

  • hypertensive elderly
  • primary open angle glaucoma in both eyes
  • ocular hypertension in both eyes

Exclusion Criteria:

acute or chronic eye inflammation cataract eye surgeries mental ill patients patients who will refuse to participate in the study other systemic /cardiovascular problem

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: Parallel Assignment
  • Masking: Single

Arms and Interventions

Participant Group / Arm
Intervention / Treatment
Experimental: Exercised group
Thirty hypertensive geriatric with high tension type primary open angle glaucoma will perform breathing exercise (alternate nostril breathing). The daily breathing exercise will be performed by the geriatrics in evening (for half an hour) and morning (for half an hour) for one month.
Thirty hypertensive geriatric with high tension type primary open angle glaucoma will perform breathing exercise (alternate nostril breathing). The daily breathing exercise will be performed by the geriatrics in evening (for half an hour) and morning (for half an hour) for one month.
No Intervention: control group
this will be a thirty-patient wait-list group that will no receive any shape of training

What is the study measuring?

Primary Outcome Measures

Outcome Measure
Measure Description
Time Frame
intraoccular pressure
Time Frame: It will be measured after 4 weeks of training
it will be measured in right and left eyes
It will be measured after 4 weeks of training

Secondary Outcome Measures

Outcome Measure
Measure Description
Time Frame
systolic blood pressure
Time Frame: It will be measured after 4 weeks of training
it will be measured sphygmomanometer
It will be measured after 4 weeks of training
diastolic blood pressure
Time Frame: It will be measured after 4 weeks of training
it will be measured sphygmomanometer
It will be measured after 4 weeks of training
heart rate
Time Frame: It will be measured after 4 weeks of training
it will be measured manually
It will be measured after 4 weeks of training
respiratory rate
Time Frame: It will be measured after 4 weeks of training
it will be measured manually
It will be measured after 4 weeks of training
hospital anxiety and depression scale
Time Frame: It will be measured after 4 weeks of training
it contains fourteen questions. it contains two sub-scales, one for anxiety and the other for depression
It will be measured after 4 weeks of training
short form 36 survey
Time Frame: It will be measured after 4 weeks of training
in general, it will assess life quality
It will be measured after 4 weeks of training
glaucoma quality of life-15 questionnaire
Time Frame: It will be measured after 4 weeks of training
it will assess glaucoma-related life quality
It will be measured after 4 weeks of training

Collaborators and Investigators

This is where you will find people and organizations involved with this study.

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)

September 15, 2022

Primary Completion (Anticipated)

January 15, 2023

Study Completion (Anticipated)

January 15, 2023

Study Registration Dates

First Submitted

October 30, 2022

First Submitted That Met QC Criteria

October 30, 2022

First Posted (Actual)

November 4, 2022

Study Record Updates

Last Update Posted (Actual)

November 4, 2022

Last Update Submitted That Met QC Criteria

October 30, 2022

Last Verified

October 1, 2022

More Information

Terms related to this study

Other Study ID Numbers

  • P.T.REC/012/004006

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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