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Simple breathing techniques may ease pain and anxiety after breast surgery

NCT ID NCT07449273

What the study statuses mean

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Recruitment status, easiest to join first

Recruiting now
This trial is taking on new participants right now.
Not yet recruiting This study
Registered, but not yet taking participants.
By invitation only
Not open to general applications. Only people the study team invites can take part.
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Paused for now. It may or may not start again.
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Running, but no longer taking on new participants.
Completed
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 Results may not be published yet.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.

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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

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

Summary

This study tests whether two types of breathing exercises—pranayama and pursed-lip breathing—can reduce pain, anxiety, and improve vital signs in women after breast surgery. 126 participants will be randomly assigned to one of three groups: pranayama, pursed-lip breathing, or standard care. The exercises are done three times daily for five minutes, starting four hours after surgery. Outcomes are measured on the first and second days after surgery.

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 (pranayama and pursed-lip breathing)
What this could lead to
If it works, this could offer a simple, drug-free way to ease pain and anxiety after breast surgery.
What could go wrong
This is a small, early-stage trial with no blinding, so results may be influenced by placebo effects. The exercises are short-term and may not work for everyone.

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

About 126 people

The number the study aims to enrol. It can still change while the study runs.

Expected to start

May 2026

An estimate. Start dates often move.

Expected to finish

Apr 2027

An estimate. End dates often move.

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

18 years and older

Sex

Female participants only

Healthy volunteers

Not accepted

This study is not open to healthy volunteers. The entry requirements below say who it is open to.

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: * Adults aged 18 years and older * Able to communicate effectively * Patients undergoing elective surgery for the first time, including radical mastectomy, modified radical mastectomy, or simple mastectomy Exclusion Criteria: * Patients undergoing breast-conserving surgery * Patients who develop any postoperative complications, such as bleeding or anesthesia-related complications * Individuals with cognitive or mental impairments * Patients who wish to withdraw from the study at any stage * Patients with hearing or speech impairments * Patients with a psychiatric diagnosis or those using psychiatric medications * Patients unable to comply with breathing exercises

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Conditions

The condition(s) this trial relates to.

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