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Clinical Trials/NCT06174870
NCT06174870Not yet recruitingNot Applicable

The Effect of Inspiratory Muscle Training on Blood Pressure and Functional Capacity in Elderly With Hypertension

University of Phayao1 site in 1 country24 target enrollmentStarted: December 10, 2023Last updated:
Conditions
Interventions

Trial Snapshot

Phase
Not Applicable
Status
Not yet recruiting
Enrollment
24
Locations
1
Primary Endpoint
Six-minute walk distance

Study Overview

Brief Summary

The goal of this clinical trial is to investigate in elderly with hypertension . The main question it aim to answer is:

• Investigate the effect of inspiratory muscle training on inspiratory muscle strength, blood pressure and physical capacity

Participants will be random in to 2 group and measure baseline. Control group will advise to maintain normal daily life activity. and Intervention group will receive inspiratory muscle training (IMT) with 60% of Maximal inspiratory pressure. Intervention group will perform IMT 30 breaths/day, 5 days a week for 6 weeks.

after 6 weeks both group will remeasure variable again as post test

Study Design

Study Type
Interventional
Allocation
Randomized
Intervention Model
Parallel
Primary Purpose
Treatment
Masking
None

Eligibility Criteria

Ages
60 Years to 75 Years (Adult, Older Adult)
Sex
All
Accepts Healthy Volunteers
No

Inclusion Criteria

  • Elderly with hypertension
  • BMI 18.5 - 29.9 kg/m2

Exclusion Criteria

  • Unstable angina
  • Resting heart rate more than 120 bpm
  • Resting blood pressure more than 180/100 mmHg
  • Other abnormality with contribute to IMT and variable measurement

Arms & Interventions

Control

No Intervention

Control group

Intervention

Experimental

IMT group

Intervention: Inspiratory muscle training (Other)

Outcomes

Primary Outcomes

Six-minute walk distance

Time Frame: "baseline, pre-intervention" and "6 weeks"

Systolic and diastolic blood pressure

Time Frame: "baseline, pre-intervention" and "6 weeks"

blood pressure will include systolic and diastolic blood pressure

Maximal Inspiratory pressure

Time Frame: "baseline, pre-intervention" and "6 weeks"

Secondary Outcomes

No secondary outcomes reported

Investigators

Sponsor Class
Other
Responsible Party
Principal Investigator
Principal Investigator

EAKARACH WONGSAYA

Lecturer

University of Phayao

Study Sites (1)

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