Bedside yoga may ease postpartum depression and strengthen Mother-Infant bond
NCT ID NCT07515222
First seen Jun 24, 2026 · Last updated Jun 27, 2026 · Updated 1 time
Summary
This study tests whether a 3-week bedside yoga program, added to standard depression treatment, can improve mother-infant bonding and reduce depression in new mothers. Fifty-two mothers with perinatal depression will be randomly assigned to yoga plus usual care or usual care alone. Researchers will measure bonding, depression scores, and levels of oxytocin and cortisol in the blood.
What this could mean
Our plain-language read of the trial. This is informational only, not medical advice or a prediction.
- Active substance
- Add-on Yoga Intervention
- What this could lead to
- If it works, this could offer a safe, drug-free way to help new mothers with depression bond better with their babies.
- What could go wrong
- This is a small early-stage trial with only 52 participants, so results may not apply widely. The yoga is added to usual medication, so benefits may be modest.
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 52 people
The number the study aims to enrol. It can still change while the study runs.
- Expected to start
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Apr 2026
An estimate. Start dates often move.
- Expected to finish
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May 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 45 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: * • Mothers aged 19 to 45 years presenting with an index depressive episode with onset either antenatally or within 12 months following childbirth and having a living child aged 0 to 28 months at time of enrolment * Edinburgh Postnatal Depression Scale (EPDS) score of 13 or above3 * Willing to participate and provide written informed consent Exclusion Criteria: * • Severe mental health conditions including psychotic features * Active suicidal ideation or infanticidal ideas * Active substance dependence (excluding nicotine) * Unstable medical condition * Extreme physical limitation precluding yoga participation * Visual or auditory impairment
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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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