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C-Section recovery gets a High-Tech boost: music, breathing, and VR put to the test

NCT ID NCT07551401

Symptom relief Sponsor: Selcuk University Source: ClinicalTrials.gov ↗

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 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.
Paused
Paused for now. It may or may not start again.
Ongoing
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 Results may not be published yet.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.

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This status has not been confirmed recently, so it may be out of date.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 26, 2026 · Last updated Jun 27, 2026 · Updated 1 time

Summary

This study compares three non-drug approaches—music therapy, breathing exercises, and virtual reality—against standard care for women recovering from cesarean section. Researchers will measure pain, gastrointestinal symptoms, and overall recovery quality in 192 participants. The goal is to find safe, effective ways to improve comfort and speed recovery without medication.

What this could mean

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

Active substance
Music therapy, breathing exercises, virtual reality
What this could lead to
If successful, this could provide simple, drug-free options to help women recover more comfortably after cesarean section.
What could go wrong
This is a small, early-stage trial with no blinding, so results may be influenced by placebo effects or participant expectations.

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 192 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

Mar 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: * Women aged 18 years and older * Able to speak and understand Turkish * Gestational age between 37 and 42 weeks * Undergoing cesarean section under spinal anesthesia * Able to communicate and willing to participate * No major intraoperative or early postoperative complications (within 0-12 hours), such as severe hemorrhage (\>1000 mL), anesthesia-related cardiorespiratory complications, major surgical complications, wound dehiscence, sepsis, or need for intensive care * No visual or hearing impairments * Having a live, healthy, singleton newborn Exclusion Criteria: * Passage of flatus before the intervention * Presence of any diagnosed medical condition during pregnancy * Development of maternal postpartum complications such as postpartum hemorrhage (\>1000 mL), infection, wound dehiscence, sepsis, thromboembolism, or need for intensive care * Presence of neonatal complications such as neonatal distress requiring intensive care, congenital anomalies, severe respiratory distress, infection, or perinatal mortality * History of chronic pain, gastrointestinal disease, or respiratory disease * Diagnosed and treated psychiatric disorders

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Conditions

The condition(s) this trial relates to.

Pain, Postoperative

As listed by the trial registrant

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

Cesarean section Cesarean section pain Gastrointestinal symptoms Obstetric recovery

How to take part

Only the study team decides who joins. These are the ways to reach them.

  1. The places running it

    1 site. The list below names each one and where it is.

  2. The official record

    ClinicalTrials.gov lists the study team's own contact details, including names and phone numbers. We don't republish those.

    Open the record ↗

  3. A doctor treating you

    A doctor who knows your case can contact a study site on your behalf, and can tell you whether this study is worth pursuing at all.

Contacts and locations

Locations

  • Konya City Hospital

    Konya, 42020, Turkey (Türkiye)

More trials for these conditions

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