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Social media and body image: hidden links to postpartum depression?

NCT ID NCT07603063

Knowledge-focused Sponsor: Sun Yat-sen University Source: ClinicalTrials.gov ↗

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.
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 Results may not be published yet.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This status has not been confirmed recently, so it may be out of date.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 27, 2026 · Last updated Jun 27, 2026

Summary

This study will survey 385 women who gave birth within the past 4 weeks to 12 months to understand how often postpartum depression occurs and how it relates to body image dissatisfaction, self-objectification, and comparing appearances on social media. Participants answer online questionnaires about their feelings and social media use. The goal is to identify factors that may contribute to postpartum depression.

What this could mean

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

What this could lead to
If this study finds strong links, it could point toward new ways to identify women at risk for postpartum depression based on body image and social media habits.
What could go wrong
This is an observational study, not a treatment trial. It cannot prove cause and effect, and results may not apply to all populations.

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.

Participants

About 385 people

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

Expected to start

Apr 2026

An estimate. Start dates often move.

Expected to finish

Oct 2026

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.

Who is studied

puerperae from 4 weeks to 12 months postpartum

Ages

18 years and older

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: 1. Aged ≥ 18 years; 2. Between 4 weeks and 12 months postpartum; 3. Able to read and comprehend the Chinese questionnaire, and capable of using a smartphone; 4. Voluntary participation in the study with a signed written informed consent form. Exclusion Criteria: 1. A confirmed pre-pregnancy diagnosis of psychiatric disorders or intellectual disabilities, preventing normal communication; 2. Diagnosed with depression during pregnancy or the postpartum period, and currently receiving pharmacological or psychological therapy; 3. Experiencing severe pregnancy or postpartum complications with an unstable clinical condition, rendering the participant unable to complete the questionnaire; 4. Having a newborn with congenital malformations or severe medical conditions; 5. Having experienced major stressful life events within the past 4 to 6 weeks (e.g., perinatal fetal death, or the death of an immediate family member).

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Conditions

The condition(s) this trial relates to.

postpartum depression

As listed by the trial registrant

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

Postpartum depression

How to take part

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

  1. 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 ↗

  2. 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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