Jacobson's Progressive Muscle Relaxation Technique With Aerobic Exercise on Cardiopulmonary Parameters and Quality of Life in Stage 1 Hypertensive Individuals

Not Applicable

Recruiting

• Conditions: Hypertension

• Registration Number: NCT06997445
• Lead Sponsor: Foundation University Islamabad

Brief Summary

The study is a randomized controlled trial. The purpose of study is to compare the additive effects of Jacobson's progressive muscle relaxation technique with aerobic exercise versus aerobic exercise on cardiopulmonary parameters including systolic and diastolic blood pressure, heart rate, respiratory rate, rate pressure product and quality of life in stage 1 hypertensive individuals.

Detailed Description

The study will consist of referred stage 1 hypertensive patients by medical specialist/cardiologist.

Participants will be screened through PAR-Q and IPAQ Questionnaire. Cardiac monitor will be used for assessing the cardiopulmonary parameters. SF-36 Questionnaire will be used for assessing the quality of life. Informed written consent will be taken after which participants will be recruited into two groups.

Control group will be provided aerobic exercise while interventional group will be provided Jacobson's progressive muscle relaxation technique with aerobic exercise.

Outcome measures assessment will be done at pre-session, at 2 weeks and after 4 weeks post-intervention

Study Timeline

• Study Start: 2024-08-02
• Status Verified: 2025-05
• Study First Submitted: 2025-05-14
• Study First Submitted QC: 2025-05-21
• Last Update Submitted: 2025-05-21
• Study First Posted: 2025-05-30
• Last Update Posted: 2025-05-30
• Primary Completion: 2025-06-05
• Study Completion: 2025-06-05

Recruitment & Eligibility

• Status: RECRUITING
• Sex: All
• Target Recruitment: 40

Inclusion Criteria

• Adults: aged (18-45 years)
• Gender: both male and female
• Patients diagnosed with stage 1 hypertension (130-139 / 80-89 mmHg according to AHA/ACC 2017 guidelines
• Mild to moderate physical activity level on IPAQ Questionnaire
• Individuals who are able to understand and follow the instructions for exercise

Exclusion Criteria

• Unstable angina, MI, heart failure, advanced CAD patients
• Severe neurological, musculoskeletal, or gynaecological conditions which limit participation in study
• Recent history of fracture
• Morbidly obese (BMI > 40.0 kg / m2)

Study & Design

• Study Type: INTERVENTIONAL
• Study Design: PARALLEL

Primary Outcome Measures

Name	Time	Method
Systolic and diastolic blood pressure	04 Weeks	Evaluation will be done using cardiac monitor for blood pressure.
Heart rate	04 Weeks	It will be measured through pulse oximeter.
Respiratory rate	04 Weeks	It will be measured by counting the number of breaths a person takes per minute
Rate pressure product	04 Weeks	It will be calculated by multiplying heart rate with systolic blood pressure

Trial Locations

Locations (1)

Foundation University College of Physical Therapy, Islamabad, 44000; 🇵🇰 Islamabad, Pakistan