Actively Recruiting

Phase Not Applicable
Age: 30Years - 65Years
All Genders
NCT07573683

Additional Effect of Coherent Breathing With Aerobic Exercise on Cardiopulmonary Parameters and Quality of Life in Stage 1 Hypertensive Individuals

Led by Foundation University Islamabad · Updated on 2026-05-07

40

Participants Needed

1

Research Sites

10 weeks

Total Duration

On this page

AI-Summary

What this Trial Is About

This study will use a randomized controlled trial to evaluate the added effects of coherent breathing combined with aerobic exercise versus aerobic exercise alone in 40 adults aged 30-65 with stage 1 hypertension. Participants will be randomly assigned to an intervention group (aerobic exercise plus coherent breathing) or a control group (aerobic exercise only) and will undergo a 4-week program with 5 sessions per week. Cardiopulmonary parameters-including blood pressure, heart rate, respiratory rate, and rate pressure product-will be measured, and quality of life will be assessed using the MINICHAL questionnaire at baseline, 2 weeks, and post-intervention. Data will be analyzed using SPSS version 21.0. The study aims to determine whether coherent breathing provides additional benefits, offering a cost-effective, non-pharmacological strategy for hypertension management in low-resource settings.

CONDITIONS

Official Title

Additional Effect of Coherent Breathing With Aerobic Exercise on Cardiopulmonary Parameters and Quality of Life in Stage 1 Hypertensive Individuals

Who Can Participate

Age: 30Years - 65Years
All Genders

Eligibility Criteria

Eligible

You may qualify if you...

  • Both male and female genders.
  • Adults aged 30-65 years.
  • Diagnosed with stage 1 hypertension (130-139/80-89 mmHg) according to ACC/AHA 2017 guidelines.
  • Mild to moderate physical activity level on IPAQ questionnaire.
  • Able to understand and follow the instructions.
Not Eligible

You will not qualify if you...

  • Diagnosed uncontrolled hypertensive patients.
  • Unstable angina, myocardial infarction, heart failure, advanced coronary artery disease, COPD, or asthma.
  • Severe neurological, musculoskeletal, or gynecological conditions limiting participation.
  • Recent history of fracture.

AI-Screening

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Complete this quick 3-step screening to check your eligibility

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Trial Site Locations

Total: 1 location

1

Foundation University Islamabad

Islamabad, Pakistan

Actively Recruiting

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Research Team

K

Kainat Zahra, MSPT-CPPT

CONTACT

S

Syeda Sumaira Batool, MSPT-CPT

CONTACT

How is the study designed?

Study Type

INTERVENTIONAL

Masking

NONE

Allocation

RANDOMIZED

Model

PARALLEL

Primary Purpose

TREATMENT

Number of Arms

2

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