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Combined Effects of Alternate Nostril Breathing and Aerobic Interval Training on Blood Pressure and Heart Rate Products in Patients With Hypertension

F

Foundation University Islamabad

Status

Enrolling

Conditions

Hypertension (HTN)

Treatments

Other: interventional group A
Other: Experimental Group

Study type

Interventional

Funder types

Other

Identifiers

NCT07177989
FUI/CTR/2025/92

Details and patient eligibility

About

Hypertension (HTN) is the foremost preventable risk factor for cardiovascular disease (CVD) and all-cause mortality, contributing to over 7 million deaths annually within the nearly 17 million attributed to CVD. Effective management through lifestyle modifications, including aerobic exercises specifically interval training presents a promising avenue for blood pressure regulation by promoting vasodilation and regulating the autonomic nervous system. Likewise, alternate nostril breathing has demonstrated efficacy in lowering blood pressure by optimizing oxygenation and improving endothelial function but their combined effect on BP measures is yet to be determined. Hence this study aims to determine the combined effects of aerobic interval training with and without alternate nostril breathing on blood pressure, rate pressure product and quality of life in patients with hypertension.

Enrollment

36 estimated patients

Sex

All

Ages

25 to 50 years old

Volunteers

No Healthy Volunteers

Inclusion criteria

  • Adults aged 25- 50 years -males and females
  • Patients diagnosed with stage 1 hypertension 130 - 139 / 80 - 89 mmHg and stage 2 hypertension, BP level ≥140/90 mmHg. according to AHA/ACC 2017 Guidelines-Individuals who are able to understand and follow the instructions for exercise

Exclusion criteria

  • Diagnosed with any current infections
  • subjects with diagnosed musculoskeletal or neurological conditions which hinder participation in physical activity program
  • Active Smokers
  • Those with any contraindication to exercise testing or training.
  • Pregnant females

Trial design

Primary purpose

Treatment

Allocation

Randomized

Interventional model

Parallel Assignment

Masking

None (Open label)

36 participants in 2 patient groups

Interventional group (Group B)
Experimental group
Description:
Patients in this group will perform alternative nostril breathing along with aerobic interval training. A protocol of total 5 weeks. Three sessions per week on alternate days will be done under the supervision of physiotherapist. All outcome measurements would be performed first at baseline and terminal after the 5 weeks intervention period
Treatment:
Other: Experimental Group
Interventional group (Group A)
Active Comparator group
Description:
Patients in tis group will perform aerobic interval training. A protocol of total 5 weeks. Three sessions per week on alternate days will be done under the supervision of physiotherapist. All outcome measurements would be performed first at baseline and terminal after the 5 weeks intervention period
Treatment:
Other: interventional group A

Trial contacts and locations

1

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Central trial contact

Zara Khalid, PhD; Sameen Fatima, DPT

Data sourced from clinicaltrials.gov

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