- ICH GCP
- US Clinical Trials Registry
- Clinical Trial NCT05605743
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
Conditions
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
- Name: ali ismail, lecturer
- Phone Number: 02 01005154209
- Email: ali.mohamed@pt.cu.edu.eg
Study Contact Backup
- Name: mona taha, professor
- Email: monaday2007@yahoo.com
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.
Sponsor
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
Additional Relevant MeSH Terms
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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