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Simple relaxation technique may ease C-Section recovery

NCT ID NCT07384637

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 Results may not be published yet.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This status has not been confirmed recently, so it may be out of date.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 progressive relaxation exercises and planned training can reduce pain, anxiety, and improve comfort in women after cesarean section. 129 new mothers participated, performing breathing and muscle relaxation exercises starting the day after surgery. Researchers measured pain, anxiety levels, and comfort using standard questionnaires.

What this could mean

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

Active substance
progressive relaxation exercises and planned training
What this could lead to
If effective, this simple, drug-free approach could help new mothers recover more comfortably after cesarean section by reducing pain and anxiety.
What could go wrong
This is a small, completed study without a control group for comparison, so results may not be generalizable. The benefits may vary based on individual factors.

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

129 people

The number who actually took part.

Started

Jan 2023

Finished

Dec 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

19 to 35 years

Sex

Female participants only

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: * on the first postoperative day, * at least four hours after analgesic administration, * mobilized, * with their baby present, * their baby without any health problems, * without any physical or mental illness, * without communication problems, * who volunteered to participate were included in the study. Exclusion Criteria: * women who were not present on the first postoperative day, * had not received analgesic treatment for at least four hours, * were not mobile, * did not have their baby with them, * their baby had any health problems, * they had a physical or mental illness, * they had difficulty communicating, * they did not volunteer to participate were excluded from the study.

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Conditions

The condition(s) this trial relates to.

anxiety disorder Motor Activity Pain

As listed by the trial registrant

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

Contacts and locations

Locations

  • Sivas Cumhuriyet University

    Sivas, Turkey (Türkiye)