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Effect of Mental and Physical Training on Blood Pressure

Not Applicable
Completed
Conditions
Elevated Blood Pressure
Interventions
Other: Mental & physical training
Other: Physical training
Other: Mental training
Other: DASH diet
Registration Number
NCT05533268
Lead Sponsor
Universiti Tunku Abdul Rahman
Brief Summary

Elevated blood pressure or prehypertension is highly associated with increased risk of developing hypertension, cardiovascular event, and type II diabetes. Many physically inactive young adults, particularly in Malaysia have blood pressure higher than normal range, therefore it is important to control the blood pressure within normal range as prophylactic measure. This experimental research will be carried out to study the effect of physical training (aerobic exercise) and mental training (mindfulness meditation) with diet as a control group on the systolic blood pressure, diastolic blood pressure and resting heart rate among young adult with elevated blood pressure living a sedentary lifestyle. Participant will be divided into 2 experimental groups (mental and physical training) and 1 control group (Dietary Approaches to Stop Hypertension -DASH diet plan) who need to complete the prescribed intervention for 6 weeks. Results will be analysed by repeated measures ANOVA followed by post-hic test.

Detailed Description

Not available

Recruitment & Eligibility

Status
COMPLETED
Sex
Male
Target Recruitment
62
Inclusion Criteria
  • Male adults aged 18-25 years
  • Normal BMI (18.5-24.9)
  • Physically inactive
  • SBP between 120-139 mmHg and/or DBP between 60-89 mmHg
  • No hearing abnormalities
  • Willing to participate
Exclusion Criteria
  • Participants who have cardiovascular, musculoskeletal, and neurological disorders or any other medical condition that would restrict them to participate in the exercise
  • Those who are taking antihypertensive medications or other medications that will affect their BP and heart rate
  • Participants who are currently engaging in any form of relaxation techniques such as yoga or meditation
  • Individuals who are actively engaged in physical activities

Study & Design

Study Type
INTERVENTIONAL
Study Design
PARALLEL
Arm && Interventions
GroupInterventionDescription
Mental and Physical TrainingMental & physical trainingCombination of mindfulness meditation and continuous moderate-intensity training for 6 weeks.
Physical TrainingPhysical trainingContinuous moderate-intensity training for 6-weeks.
Mental TrainingMental trainingmindfulness meditation for 6-weeks.
DASH Diet PlanDASH dietDietary Approaches to Stop Hypertension for 6-weeks.
Primary Outcome Measures
NameTimeMethod
Change from Baseline Diastolic Blood Pressure at 6 weeks.At baseline over a period of 6 weeks.

Diastolic blood pressure (DPB) will be measured at baseline (before intervention begin), after 3 weeks of intervention, and post 6-weeks of intervention.

Change from Baseline Systolic Blood Pressure at 6 weeks.At baseline over a period of 6 weeks.

Systolic blood pressure (SPB) will be measured at baseline (before intervention begin), after 3 weeks of intervention, and post 6-weeks of intervention.

Change from Baseline Mean Arterial Pressure at 6 weeks.At baseline over a period of 6 weeks.

Mean arterial pressure (MAP) will be measured at baseline (before intervention begin), after 3 weeks of intervention, and post 6-weeks of intervention.

Change from Baseline Resting Heart Rate at 6 weeks.At baseline over a period of 6 weeks.

Resting heart rate (RHR) will be measured at baseline (before intervention begin), after 3 weeks of intervention, and post 6-weeks of intervention.

Change from Baseline Pulse Pressure at 6 weeks.At baseline over a period of 6 weeks.

Pulse pressure will be measured at baseline (before intervention begin), after 3 weeks of intervention, and post 6-weeks of intervention.

Secondary Outcome Measures
NameTimeMethod
Change from Baseline Body Mass Index at 6 weeks.At baseline over a period of 6 weeks.

Body mass index (BMI) will be measured at baseline (before intervention begin), after 3 weeks of intervention, and post 6-weeks of intervention.

Trial Locations

Locations (1)

Universiti Tunku Abdul Rahman

🇲🇾

Kajang, Selangor, Malaysia

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