Device guided breathing for essential hypertensio
Not Applicable
- Conditions
- Health Condition 1: I10- Essential (primary) hypertension
- Registration Number
- CTRI/2022/08/044793
- Lead Sponsor
- Patanjali Research Foundation Trust
- Brief Summary
Not available
- Detailed Description
Not available
Recruitment & Eligibility
- Status
- ot Yet Recruiting
- Sex
- Not specified
- Target Recruitment
- 0
Inclusion Criteria
1. Diagnosed with essential hypertension i.e. having average blood pressure of 3 recordings, systolic equal or more than 140 mmHg and/or diastolic equal or more than 90 mmHg, or previously diagnosed as hypertensive, or regular intake of antihypertensive drug.
2. Willingness to participate in the study.
Exclusion Criteria
1. Patients with secondary hypertension, respiratory disorders, malignancy, extra systole and recent surgery will be excluded.
2. Pregnant women will be excluded.
Study & Design
- Study Type
- Interventional
- Study Design
- Not specified
- Primary Outcome Measures
Name Time Method 1. Blood pressure <br/ ><br>2. Heart rate variability <br/ ><br>3. Respiration rate <br/ ><br>4. Oxygen saturation <br/ ><br>Timepoint: 1. Before the intervention [5 minutes] <br/ ><br>2. Training [2 minutes] <br/ ><br>3. During the intervention [11 minutes] <br/ ><br>4. After the intervention [5 minutes] <br/ ><br> <br/ ><br>
- Secondary Outcome Measures
Name Time Method 1. Spielberger State Trait <br/ ><br>Anxiety Inventory <br/ ><br>2. The Brief Mood Introspective ScaleTimepoint: 1. After pre and before training. <br/ ><br>2. After the intervention and before post.;3. Nijmegen questionnaire (NQ) <br/ ><br>4. Visual analogue scale (VAS) <br/ ><br>Timepoint: 1. After the intervention and before post.