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Efficacy of Shitali Respiratory Rehabilitation Program in Obstructive Sleep Apnea

Cairo University (CU) logo

Cairo University (CU)

Status

Enrolling

Conditions

Obstructive Sleep Apnea

Treatments

Behavioral: shitali pranayama respiratory rehabilitation training

Study type

Interventional

Funder types

Other

Identifiers

NCT06715228
IRB00014233-15

Details and patient eligibility

About

obstructive sleep apnea has a negative impact on blood pressure of patients, sleeping quality, and respiration

Full description

in this study, patients (n=40) with obstructive sleep apnea will participate in this study to be divided in to group I and group II with an equal number of patients (n = 20 for the group). Group I 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, the other group, Group II, will act as control group.

Enrollment

40 estimated patients

Sex

All

Ages

35 to 55 years old

Volunteers

No Healthy Volunteers

Inclusion criteria

  • non-obese patients
  • obstructive sleep apnea (mild and moderate form)

Exclusion criteria

  • cardiac patients metabolic diseases kidney diseases

Trial design

Primary purpose

Treatment

Allocation

Randomized

Interventional model

Parallel Assignment

Masking

Single Blind

40 participants in 2 patient groups

group I
Experimental group
Description:
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,
Treatment:
Behavioral: shitali pranayama respiratory rehabilitation training
Group II
No Intervention group
Description:
in 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

Trial contacts and locations

1

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Central trial contact

Ali Isamil, Lecturer; ahmed elfahl, Lecturer

Data sourced from clinicaltrials.gov

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