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Simple breathing exercises cut frailty in elderly COPD patients

NCT ID NCT07472530

What the study statuses mean

This study's is highlighted.

Recruitment status, easiest to join first

Recruiting now
This trial is taking on new participants right now.
Not yet recruiting
Registered, but not yet taking participants.
By invitation only
Not open to general applications. Only people the study team invites can take part.
Paused
Paused for now. It may or may not start again.
Ongoing
Running, but no longer taking on new participants.
Completed This study
The trial has finished. Results may not be published yet.
Stopped early
Stopped early, before it reached the end. That can be for many reasons, including safety.
Cancelled
Cancelled before anyone took part.

Expanded access (not trials)

Expanded access
Not a trial. This treatment can be requested outside a study, case by case, for people who qualify.
Expanded access (paused)
Not a trial. The treatment can normally be requested outside a study, but is unavailable right now.
Expanded access (ended)
Not a trial. The treatment could once be requested outside a study, but no longer can.
Approved
The treatment has been approved, so it is available normally rather than through this programme.

When the status isn't known

Details not published
The full record has not been published yet, so there is little to show here.
Status unknown
This status has not been confirmed recently, so it may be out of date.

First seen Jun 27, 2026 · Last updated Jun 27, 2026

Summary

This study tested whether a six-week program of breathing exercises using a device called an incentive spirometer could help older adults (65+) with COPD who were also frail. 66 participants were split into two groups: one did the breathing exercises, the other did not. After six weeks, those who did the exercises showed better lung function, could walk farther, felt less short of breath, and had lower frailty scores. The results suggest that adding simple breathing exercises to COPD care might improve both physical strength and quality of life in older patients.

What this could mean

Our plain-language read of the trial. This is informational only, not medical advice or a prediction.

Active substance
breathing exercises using an incentive spirometer (Triflow device)
What this could lead to
If confirmed, this simple breathing exercise program could become a standard part of COPD care for older adults, helping them feel stronger and breathe easier.
What could go wrong
This was a small, single-blind trial with 66 participants, so results may not apply to everyone. The improvements were modest and need to be replicated in larger, longer studies.

This is an AI summary of the original study and may miss details. Read our disclaimer.

Study facts

What this study's own registry entry says, in plain language.

Phase

Not a phased trial

Phase numbers describe drug development. The registry uses this when they do not apply, as it does for trials of devices, procedures or behaviour changes, and for observational studies.

Participants

66 people

The number who actually took part.

Started

Aug 2023

Finished

Oct 2023

Lead sponsor

Other sponsor

The registry's catch-all category, for sponsors it does not file as a company, a government agency, or a research network.

Who can take part

This study's own entry requirements. Only the study team can say for certain whether you qualify.

Ages

65 years and older

Sex

Anyone

Healthy volunteers

Accepted

You do not need to have the condition being studied to take part.

Show the full entry requirements

Copied word for word from the study's registry entry, so the wording is the study team's rather than ours.

Inclusion Criteria: * a diagnosis of COPD for at least one year prior to participation, * age 65 years or older, * normal thoracic and vertebral spine and lower extremities, * a score of 5 or higher on the Edmonton Frailty Scale, * no participation in any pulmonary rehabilitation or exercise program within the last year Exclusion Criteria: * a history of myocardial infarction within the last 3 months, * a history of angina pectoris or cerebrovascular event within the last month, * uncontrolled arrhythmia, * heart rate \>120 beats/min, * uncontrolled hypertension (BP \>180/100 mmHg), * advanced heart failure (Stage 3/Stage 4), * severe anemia (Hb \<7 g/dL), * active or chronic infection (COPD exacerbation, Tuberculosis, Osteomyelitis, Rheumatoid Arthritis), * resting or exertional dyspnea, exertional angina, * increased cough and sputum complaints within the last week, * hospitalization within the last month, * blood transfusion within the last month * the presence of physical or mental health problems that would impede communication

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Conditions

The condition(s) this trial relates to.

As listed by the trial registrant

The condition terms exactly as the trial's registrant entered them.

Contacts and locations

Locations

  • Çerkeş State Hospital

    Çankırı, Merkez, 18100, Turkey (Türkiye)

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