Reiki after C-Section: a new way to boost recovery and mood?
NCT ID NCT07654881
First seen Jun 25, 2026 · Last updated Jun 27, 2026 · Updated 1 time
Summary
This study will test whether Reiki therapy, a gentle hands-on energy technique, can improve recovery, comfort, and mood in women who have had a cesarean section. Eighty new mothers will receive three Reiki sessions on days 1, 2, and 7 after birth, in addition to standard care. Researchers will measure healing, comfort, and emotional well-being to see if Reiki offers any extra benefit.
What this could mean
Our plain-language read of the trial. This is informational only, not medical advice or a prediction.
- Active substance
- Reiki therapy
- What this could lead to
- If it works, this could offer a simple, side-effect-free way to help mothers feel better and recover more comfortably after a C-section.
- What could go wrong
- This is a small, early-stage study with only 80 participants. Reiki's effects are hard to measure, and any benefits may be due to relaxation or placebo rather than the therapy itself.
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
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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
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About 80 people
The number the study aims to enrol. It can still change while the study runs.
- Expected to start
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Jun 2026
An estimate. Start dates often move.
- Expected to finish
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Jan 2027
An estimate. End dates often move.
- Lead sponsor
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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
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19 to 35 years
- Sex
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Female participants only
- Healthy volunteers
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Not accepted
This study is not open to healthy volunteers. The entry requirements below say who it is open to.
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Copied word for word from the study's registry entry, so the wording is the study team's rather than ours.
Inclusion Criteria: * Ages 19-35 * Literate and able to communicate * Those who gave birth after 37 weeks of gestation * Those who had a single or intrauterine delivery * Those who meet the inclusion criteria and volunteer to participate * Those residing within the central district of Gaziantep province * Those who received spinal/epidural anesthesia Exclusion Criteria: * Having an infectious skin disease * Having a chronic illness (diabetes mellitus, hypertension, etc.) * Having complications related to the birth process * The baby not being present for any reason * Using sedative agents for any reason * Mothers with disabled babies * Having experienced an acute psychiatric attack
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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.
How to take part
Only the study team decides who joins. These are the ways to reach them.
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The official record
ClinicalTrials.gov lists the study team's own contact details, including names and phone numbers. We don't republish those.
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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.
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Other studies related to the condition(s) this trial covers.
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