Study Results
The study team has not published outcome measurements, participant flow, or safety data for this trial yet. Check back later for updates.
Basic Information
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RECRUITING
NA
100 participants
INTERVENTIONAL
2026-02-05
2026-04-13
Brief Summary
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Detailed Description
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Conditions
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Study Design
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RANDOMIZED
PARALLEL
PREVENTION
TRIPLE
Study Groups
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control group
No interventions assigned to this group
Pranayama group
pranayama breathing exercises
In this study, a pranayama breathing exercise protocol lasting approximately 14-15 minutes will be applied, aiming to increase relaxation and physiological well-being. Participants will prepare for the exercise in a supported and comfortable sitting position, breathing through the nose. The protocol consists of 3 minutes of diaphragmatic breathing, 5 minutes of alternate nostril breathing (Nadī Shodhana), 3 minutes of Ujjayi breathing, and 3 minutes of long, slow exhalation techniques. The exercises will be conducted with one-on-one guidance by a trained researcher; participants' comfort and any signs of discomfort will be monitored, and the exercise will be terminated if necessary.
Interventions
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pranayama breathing exercises
In this study, a pranayama breathing exercise protocol lasting approximately 14-15 minutes will be applied, aiming to increase relaxation and physiological well-being. Participants will prepare for the exercise in a supported and comfortable sitting position, breathing through the nose. The protocol consists of 3 minutes of diaphragmatic breathing, 5 minutes of alternate nostril breathing (Nadī Shodhana), 3 minutes of Ujjayi breathing, and 3 minutes of long, slow exhalation techniques. The exercises will be conducted with one-on-one guidance by a trained researcher; participants' comfort and any signs of discomfort will be monitored, and the exercise will be terminated if necessary.
Eligibility Criteria
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Inclusion Criteria
* Reported a post-operative pain level of at least 4 on the Numerical Rating Scale (NRS)
* Knowledge of Turkish
* Ability to communicate effectively with the research team
* Volunteer to participate in the study and provide written consent
Exclusion Criteria
* Presence of pregnancy complications (e.g. pre-eclampsia, gestational diabetes, placenta praevia)
* History of chronic pain or analgesic dependence
* Requirement for admission to the intensive care unit in the early postoperative period
* Need for additional surgical intervention
* Development of significant intraoperative or postoperative complications
* Refusal to exercise or intolerance to exercise
* Failure to comply with study procedures
* Withdrawal of consent
* Incomplete follow-up
* Development of a new medical condition during the study that could affect the results
18 Years
35 Years
FEMALE
Yes
Sponsors
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KTO Karatay University
OTHER
Responsible Party
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Hafize Dağ Tüzmen
Asst.Prof.
Locations
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Kto Karatay University
Konya, , Turkey (Türkiye)
Countries
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Facility Contacts
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Other Identifiers
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Pranayama
Identifier Type: -
Identifier Source: org_study_id
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