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A study of a randomized control trial of the effect of respiratory muscle training on suppressing recurrence of pneumonia in older people

A study of a randomized control trial of the effect of respiratory muscle training on suppressing recurrence of pneumonia in older people - Respiratory muscle training and recurrence of pneumonia in older people

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
JPRN
Registry ID
JPRN-UMIN000047619
Enrollment
240
Registered
2022-05-02
Start date
2022-05-09
Completion date
Unknown
Last updated
2026-06-29

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

Conditions

Pneumonia in older people

Interventions

Respiratory muscle training + fortification + rehabilitation. The respiratory muscle training machines are set at a resistance value of 50-80% of the maximum respiratory muscle strength. The patie
rehabilitation

Sponsors

Tohoku University
Lead Sponsor

Eligibility

Sex/Gender
All

Inclusion criteria

Inclusion criteria: Older pneumonia patients requiring hospitalization aged 70 years and older, regardless of gender. Patients that can tolerate standard treatments for pneumonia according to the guidelines. Patients with a cognitive function test MMSE score 10 and higher, who can perform respiratory muscle training.

Exclusion criteria

Exclusion criteria: Cancer patients managed within the past 5 years, patients with pacemakers (muscle mass and fat mass cannot be measured), postoperative pneumonia, intubated patients, patients with tracheostomy. Patients that are prone to pneumothorax such as severe interstitial pneumonia and chronic obstructive pulmonary disease, patients whose blood pressure rising is danger such as aortic aneurysm and severe heart failure, patients with severe renal failure (before introduction of dialysis), septic patients, patients with tube feeding, gastric fistula, immunodeficiency patients such as taking immunosuppressive agents or dialysis, patients with multiple fractures of ribs, patients with severe dementia and etc.

Design outcomes

Primary

MeasureTime frame
The primary endpoint is the recurrence rate of pneumonia in the intervention and the control group for 1 year after the beginning of the training. We will observe the presence of superiority of the intervention group to the control group.

Countries

Japan

Contacts

Public ContactRyuuko Ishimoda

Tohoku University Graduate School of Medicine Department of Physical Medicine and Rehabilitation

ishimoda@med.tohoku.ac.jp0227177338

Outcome results

None listed

Source: JPRN (via WHO ICTRP) · Data processed: Jul 3, 2026