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Not yet recruiting NCT07715019

Social Media Use and Motherhood

— Observational Postpartum Period

For patients and families

In plain language

An automatic summary of structured registry data. It is an orientation aid, not a substitute for the official protocol or a physician assessment.

What is being studied
The protocol lists: No intervention.
Who it may be relevant to
Registry conditions: Postpartum Period. Basic parameters: No limits · Female.
What needs checking
Age, condition and sex are only basic indicators. Prior treatment, laboratory values and other mandatory requirements appear in the eligibility criteria below.
Where it takes place
Spain
Next step
Save the trial, show it to the treating physician, and confirm current recruitment with the study center. Costs, documents and travel →

Unsure about the terms? Read our patient guide →

Official title

Social Media Use, Body Image Disorders, Sexuality, Sleep Quality, and Physical Activity in the Postpartum Period

Overview

This study aims to analyze the relationship between social media use, body image disorders, sexuality, sleep quality, and physical activity during the postpartum period. For this purpose, we will recruit 85 postpartum women through midwives from the Zamora Health Area. Following the signing of informed consent, participants will complete validated online questionnaires evaluating these dimensions. Participant recruitment and data collection will take place from September to December 2026.

Interventions

  • Other No intervention
    No intervention

Primary outcome measures

  • Body Image disorders [Time frame: Only at Baseline]
Secondary outcome measures (3)
  • Sleep quality [Time frame: Only at Baseline]
  • Sexuality [Time frame: Only at Baseline]
  • Physical activity [Time frame: Only at Baseline]

Eligibility criteria

Inclusion criteria

  • Women Within one year postpartum

Exclusion criteria

\-

Criteria are shown verbatim from the registry (in English). Final eligibility is always assessed by the study center.

Healthy volunteers: No

Study design

Observational model
Case-only

Study locations

Spain · 1 center
  • Jose Ignacio Recio — Zamora

Identifiers

NCT: NCT07715019 · TESIS_01

Primary sources (government registries)

View this study on ClinicalTrials.gov ↗