The Effect of Alternate Nasal Breathing Exercise ın Hypertension
NCT ID: NCT07114952
Last Updated: 2025-08-11
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
Get a concise snapshot of the trial, including recruitment status, study phase, enrollment targets, and key timeline milestones.
COMPLETED
NA
52 participants
INTERVENTIONAL
2025-01-06
2025-05-26
Brief Summary
Review the sponsor-provided synopsis that highlights what the study is about and why it is being conducted.
Related Clinical Trials
Explore similar clinical trials based on study characteristics and research focus.
Combined Effects of Alternate Nostril Breathing and Aerobic Interval Training on Blood Pressure and Heart Rate Products in Patients With Hypertension
NCT07177989
Comparison of Breathing Exercise for Hypertensive Patients
NCT05158569
Treating Hypertension With Breath Control
NCT01285193
Relaxation Breathing Exercises Effects Among Hypertensive Patients
NCT06131528
Whole Body Vibration Training Applied with Different Frequencies in Hypertensive Patients
NCT05768555
Detailed Description
Dive into the extended narrative that explains the scientific background, objectives, and procedures in greater depth.
Materials and Methods: The study sample consists of 52 patients (26 intervention and 26 control) from cardiology outpatient clinics. Ethics committee approval, institutional permissions, and verbal and written informed consent were obtained from the participants. Patients in the intervention group are instructed to perform alternate nasal breathing exercises for 10 minutes daily for four weeks, while the control group continues with routine treatment. Data collection tools include the Patient Introduction Form, Perceived Stress Scale, Life Findings Follow-up Form, and Blood Pressure Monitoring Forms. Planned statistical analyses include Independent Sample t-test, Paired Sample t-test, chi-square test, Mann-Whitney U test, and Wilcoxon test.
Conditions
See the medical conditions and disease areas that this research is targeting or investigating.
Study Design
Understand how the trial is structured, including allocation methods, masking strategies, primary purpose, and other design elements.
RANDOMIZED
PARALLEL
SUPPORTIVE_CARE
NONE
Study Groups
Review each arm or cohort in the study, along with the interventions and objectives associated with them.
alternative nasal breathing exercise intervention group
The intervention group of 26 participants practiced an alternative nasal breathing exercise. This group practiced alternate nasal breathing exercise for 4 weeks.
alternative nasal breathing
The alternate nasal breathing exercise involves breathing in and out through both nostrils in a certain pattern and for a certain period of time. For example, an individual who breathes in through the right nostril for 5 seconds with the left nostril closed, then closes the right nostril and exhales through the left nostril for 5 seconds. Then he/she inhales through the left nostril for 5 seconds and exhales through the right nostril. A total of 6 breaths are taken per minute. The application is applied for 5 minutes, the patient rests in a calm environment for two minutes and the application is performed for another 5 minutes. In order to increase the compliance of individuals with the application, a sample video was watched and application instructions were given by the researcher. The application was performed while the patients were in an upright sitting position.
control group
The group consisted of 26 participants. No intervention was administered. Participants continued their usual care without any additional exercises or treatments during the study period.
No interventions assigned to this group
Interventions
Learn about the drugs, procedures, or behavioral strategies being tested and how they are applied within this trial.
alternative nasal breathing
The alternate nasal breathing exercise involves breathing in and out through both nostrils in a certain pattern and for a certain period of time. For example, an individual who breathes in through the right nostril for 5 seconds with the left nostril closed, then closes the right nostril and exhales through the left nostril for 5 seconds. Then he/she inhales through the left nostril for 5 seconds and exhales through the right nostril. A total of 6 breaths are taken per minute. The application is applied for 5 minutes, the patient rests in a calm environment for two minutes and the application is performed for another 5 minutes. In order to increase the compliance of individuals with the application, a sample video was watched and application instructions were given by the researcher. The application was performed while the patients were in an upright sitting position.
Eligibility Criteria
Check the participation requirements, including inclusion and exclusion rules, age limits, and whether healthy volunteers are accepted.
Inclusion Criteria
* Literate,
* Diagnosed with hypertension at least 6 months ago,
* No change in hypertension medications in the last three months,
* Functionally capable of performing alternative nasal breathing exercises,
* Patients who volunteered to participate in the study were included.
Exclusion Criteria
* Patients with cognitive impairment,
* Patients practicing yoga or breathing exercises for hypertension,
* Patients with heart failure, cancer, kidney failure, or respiratory diseases were not included in the study.
18 Years
65 Years
ALL
No
Sponsors
Meet the organizations funding or collaborating on the study and learn about their roles.
Cukurova University
OTHER
Adiyaman University
OTHER
Responsible Party
Identify the individual or organization who holds primary responsibility for the study information submitted to regulators.
Leyla Senem Ün
Research assistant
Locations
Explore where the study is taking place and check the recruitment status at each participating site.
Adana City Training and Research Hospital, Cardiology Outpatient Clinic
Adana, Yüreğir, Turkey (Türkiye)
Countries
Review the countries where the study has at least one active or historical site.
Other Identifiers
Review additional registry numbers or institutional identifiers associated with this trial.
CU-SBF-LSU-01
Identifier Type: -
Identifier Source: org_study_id
More Related Trials
Additional clinical trials that may be relevant based on similarity analysis.