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A clinical trial to study the effect of Interval Inspiratory Muscle Training on Hypertensive Patients

Effect of Interval Inspiratory Muscle Training on Autonomic Dysfunction, Blood Pressure and Health Related Quality Of Life in Hypertensive Patients

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
CTRI
Registry ID
CTRI/2018/03/012294
Enrollment
26
Registered
2018-03-01
Start date
Unknown
Completion date
Unknown
Last updated
2021-11-24

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Health Condition 1: null- Hypertensive Individuals

Interventions

Intervention1: Interval Inspiratory Muscle Training: Interval inspiratory muscle training (IMT) via threshold device at 70% loads Control Intervention1: Unloaded Interval Inspiratory Muscle Training:

Sponsors

Jamia Millia Islamia
Lead Sponsor

Eligibility

Inclusion criteria

Inclusion criteria: 1. Study will include both male and female subjects 2. age >=30 and >=65 years, previously diagnosed with essential hypertension, with systolic blood pressure >=140 mmHg or diastolic blood pressure >=90 mmHg.

Exclusion criteria

Exclusion criteria: Exclusion criteria 1. Severe dyspnea 2. Severe orthopaedic, musculoskeletal, or neurological limitations 3. Significant cognitive impairment 4.A current or past history of DVT 5. A history of MI or stroke in the previous 6 months, CHF, unstable angina or pulmonary disease of any aetiology. 6. Women who are pregnant or breast feeding are excluded 7. Recent thoracic surgery or trauma will be excluded 8. The subjects with body mass index (BMI) more than 9. Potential subjects will be also excluded if they reported currently smoking, an acute infection, dementia, respiratory disorders, and dysrhythmias. 10. Individual previous diagnosis of pulmonary disease (FVC

Design outcomes

Primary

MeasureTime frame
Heart rate variability measurement Blood Pressure Health related quality of life-SF 36Timepoint: Baseline and post intervention (6 weeks)

Secondary

MeasureTime frame
Pulmonary function test 6 minute walk test Dysapnea scale Timepoint: Baseline and post intervention (6 weeks)

Countries

India

Contacts

Public ContactAdila Parveen

Centre for Physiotherapy and Rehabilitation Sciences, Jamia Millia Islamia

poojakukreti37@gmail.com9873585242

Outcome results

None listed

Source: CTRI (via WHO ICTRP) · Data processed: Feb 4, 2026