Efficacy of Shitali Respiratory Rehabilitation Program in Obstructive Sleep Apnea
1 other identifier
interventional
40
1 country
1
Brief Summary
obstructive sleep apnea has a negative impact on blood pressure of patients, sleeping quality, and respiration
Trial Health
Trial Health Score
Automated assessment based on enrollment pace, timeline, and geographic reach
participants targeted
Target at P25-P50 for not_applicable
Started Nov 2024
Shorter than P25 for not_applicable
1 active site
Health score is calculated from publicly available data and should be used for screening purposes only.
Trial Relationships
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Study Timeline
Key milestones and dates
Study Start
First participant enrolled
November 7, 2024
CompletedFirst Submitted
Initial submission to the registry
November 28, 2024
CompletedFirst Posted
Study publicly available on registry
December 4, 2024
CompletedPrimary Completion
Last participant's last visit for primary outcome
April 15, 2025
CompletedStudy Completion
Last participant's last visit for all outcomes
April 15, 2025
CompletedDecember 4, 2024
November 1, 2024
5 months
November 28, 2024
November 28, 2024
Conditions
Outcome Measures
Primary Outcomes (1)
apnea hypopnea index
it will be measured through a sleep study
it will be assessed after 12 weeks
Secondary Outcomes (6)
systolic blood pressure
it will be assessed after 12 weeks
diastolic blood pressure
it will be assessed after 12 weeks
Pittsburg sleep quality index
it will be assessed after 12 weeks
respiratory rate
it will be assessed after 12 weeks
Epworth sleepiness scale
it will be assessed after 12 weeks
- +1 more secondary outcomes
Study Arms (2)
group I
EXPERIMENTALin this group, patients (n=20) with obstructive sleep apnea will participate and will administer six cycles of 5-min shitali respiratory pranayama exercise rehabilitation training (the rehabilitation will be repeated or applied at morning, afternoon, and also at evening) for 12 week as a daily performance,
Group II
NO INTERVENTIONin this group, patients (n=20) with obstructive sleep apnea will participate and will act as control group. In this group, no intervention will be applied
Interventions
in this group, patients (n=20) with obstructive sleep apnea will participate and will administer six cycles of 5-min shitali respiratory pranayama exercise rehabilitation training (the rehabilitation will be repeated or applied at morning, afternoon, and also at evening) for 12 week as a daily performance
Eligibility Criteria
You may qualify if:
- non-obese patients
- obstructive sleep apnea (mild and moderate form)
You may not qualify if:
- cardiac patients metabolic diseases kidney diseases
Contact the study team to confirm eligibility.
Sponsors & Collaborators
- Cairo Universitylead
Study Sites (1)
faculty of physical therapy Cairo university
Dokki, Giza Governorate, Egypt
MeSH Terms
Conditions
Condition Hierarchy (Ancestors)
Study Officials
- PRINCIPAL INVESTIGATOR
Ali Ismail, lecturer
Cairo University
Central Study Contacts
Study Design
- Study Type
- interventional
- Phase
- not applicable
- Allocation
- RANDOMIZED
- Masking
- SINGLE
- Who Masked
- OUTCOMES ASSESSOR
- Purpose
- TREATMENT
- Intervention Model
- PARALLEL
- Sponsor Type
- OTHER
- Responsible Party
- PRINCIPAL INVESTIGATOR
- PI Title
- Department of Physical Therapy for Cardiovascular/Respiratory Disorder and Geriatrics, Faculty of Physical Therapy
Study Record Dates
First Submitted
November 28, 2024
First Posted
December 4, 2024
Study Start
November 7, 2024
Primary Completion
April 15, 2025
Study Completion
April 15, 2025
Last Updated
December 4, 2024
Record last verified: 2024-11