The Effect of Pranayama on Pain and Respiration After Coronary Bypass Surgery
NCT ID: NCT06485531
Last Updated: 2024-07-03
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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COMPLETED
NA
66 participants
INTERVENTIONAL
2022-03-15
2023-05-22
Brief Summary
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Detailed Description
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Conditions
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Study Design
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RANDOMIZED
SEQUENTIAL
PREVENTION
NONE
Study Groups
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Pranayama
Nadi Shothana Pranayama was applied to the patients for 15 minutes before the surgery and for 7 days after the surgery. After the application, FVC, FEV1, and FEV1/FVC values were measured with a spirometer (Contec Spirometer SP70B, Contec Medical Systems Co,. Ltd., China) and recorded in the Patient Follow-up Form. In cases where the patient did not perform well, the measurement was repeated at least three times and the best data was taken. Systolic and diastolic blood pressure, heart rate, respiratory rate, and peripheral oxygen saturation, which were thought to affect the results of FVC, FEV1, and FEV1/FVC values, were also measured and recorded. In addition, hematocrit level, analgesia dose, and amounts used during the day were recorded daily and in the Patient Follow-up Form. Pain levels were evaluated 4 times daily (10:00-14:00-22:00-06:00) during the 0th to 6th days after surgery and recorded on the Visual Analog Scale Form.
Pranamaya
Pranamaya
Pursed Lips Breathing
Pursed Lip Breathing Exercise was applied to the patients before and after the surgery for 15 minutes. After the application, FVC, FEV1, and FEV1/FVC values were measured with a spirometer (Contec Spirometer SP70B, Contec Medical Systems Co., Ltd., China) and recorded in the Patient Follow-up Form. (Annex-3). In cases where the patient did not perform well, the measurement was repeated at least three times and the best data was taken. Systolic and diastolic blood pressure, heart rate, respiratory rate, and peripheral oxygen saturation, which are thought to affect the results of FVC, FEV1, and FEV1/FVC values, were also measured and recorded before and after the application. In addition, hematocrit level, analgesia dose, and amounts used during the day were recorded daily and in the Patient Follow-up Form. Pain levels were evaluated 4 times daily (10:00-14:00-22:00-06:00) during the 0th to 6th days after surgery and recorded on the Visual Analog Scale Form.
Pursed Lips Breathing
Pursed Lips Breathing
Control
No intervention was made to the control group patients. FVC, FEV1 and FEV1/FVC values of the patients were measured with a spirometer (Contec Spirometer SP70B, Contec Medical Systems Co., Ltd., China) before the surgery and for 7 days after the surgery. In cases where the patient did not perform well, the measurement was repeated at least three times and the best data was taken. Systolic and diastolic blood pressure, heart rate, respiratory rate, and peripheral oxygen saturation, which are thought to affect the results of FVC, FEV1, and FEV1/FVC values, were also measured and recorded at 15-minute intervals. In addition, the hematocrit level, the dose, and amount of analgesia used during the day were recorded daily and in the Patient Follow-up Form. Pain levels were evaluated 4 times daily (10:00-14:00-22:00-06:00) during the 0th to 6th days after surgery and recorded on the Visual Analog Scale Form.
No interventions assigned to this group
Interventions
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Pranamaya
Pranamaya
Pursed Lips Breathing
Pursed Lips Breathing
Eligibility Criteria
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Inclusion Criteria
* Cardiopulmonary risk index score ≤2
* Those aged 18 and over,
* Being literate and communicative,
* American Society of Anesthesiologists (ASA) classification I or II,
* Preoperative respiratory function tests with normal FEV1, FVC, FEV1/FVC values,
* No complications developed during and after the surgical intervention,
* An analgesic drug with the same active ingredient is applied to control pain after surgical intervention,
* Patients who were administered antibiotics with the same active ingredient after surgical intervention were included.
Exclusion Criteria
* Cardiopulmonary risk index score ≥4
* Complications developing during or after surgery,
* Intubated,
* Those with chronic pain in the pre-surgical period,
* Those with limited movement activity before surgery,
* Having a body mass index (BMI≥30),
* Patients who could not adapt to and tolerate the pranayama technique were not included in the study.
ALL
Yes
Sponsors
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Istanbul University - Cerrahpasa
OTHER
Responsible Party
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Tugba ALBAYRAM
Principal Investigator
Principal Investigators
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Tuğba Albayram
Role: PRINCIPAL_INVESTIGATOR
University of Gaziantep
Locations
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Tuğba Albayram
Gaziantep, Şehitkamil, Turkey (Türkiye)
Countries
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Other Identifiers
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TALBAYRAM
Identifier Type: -
Identifier Source: org_study_id
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