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Simple strength tests and surveys may predict labor complications

NCT ID NCT07635771

Knowledge-focused Sponsor: Institut Investigacio Sanitaria Pere Virgili Source: ClinicalTrials.gov ↗

What the study statuses mean

This study's is highlighted.

Recruitment status, easiest to join first

Recruiting now This study
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
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 Results may not be published yet.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This status has not been confirmed recently, so it may be out of date.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 25, 2026 · Last updated Jun 27, 2026 · Updated 1 time

Summary

This observational study looks at 420 pregnant women to see if physical fitness tests (like hand grip and chair stands) and emotional surveys (about fear and confidence) can predict whether a birth will be natural or require medical help. It also checks if these factors affect breastfeeding success up to 6 months after birth. The goal is to create a tool that helps doctors identify women who may need extra support during labor.

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 successful, this could help doctors predict which women might have complications during labor, allowing for better preparation and support.
What could go wrong
This is a small, early observational study, not a treatment trial. The results may not apply to all pregnant women, and the predictions may not be accurate enough to change care.

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 420 people

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

Started

Jun 2026

Expected to finish

Dec 2027

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

The study population consists of pregnant women receiving prenatal care at the Hospital Universitari de Tortosa Verge de la Cinta (HUTVC). The sample includes healthy volunteers in their third trimester of pregnancy (\>28 weeks of gestation) with low-to-moderate obstetric risk. The population reflects a diverse group of expectant mothers who are able to perform simple physical functional tests and are interested in contributing to research on birth outcomes and breastfeeding. Participants are selected during their routine third-trimester prenatal visit at the HUTVC through non-probabilistic consecutive sampling until the required sample size of 420 participants is reached.

Ages

18 years and older

Sex

Female participants only

Healthy volunteers

Not accepted

This study is not open to healthy volunteers. The entry requirements below say who it is open to.

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: * Pregnant women aged 18 years or older * Low-to-moderate risk pregnancy * Singleton pregnancy * Third trimester of pregnancy (\>28 gestational weeks) * Understanding of the official languages * Acceptance and signing of the participant information sheet and informed consent form * Availability of an electronic device to complete the forms Exclusion Criteria: * Medical contraindication for light physical activity * Severe cardio-respiratory or musculoskeletal pathology * Elective cesarean section * Severe fetal malformations

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Conditions

The condition(s) this trial relates to.

Breast Feeding Motor Activity obstetric disorder Obstetric Labor Complications pregnancy disorder

As listed by the trial registrant

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

Breastfeeding Hand strength Labor (obstetrics)--complications Labor and childbirth Physical conditioning, human Self efficacy Tocophobia

How to take part

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

  1. The places running it

    1 site. The list below names each one and where it is.

  2. 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 ↗

  3. 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.

Contacts and locations

Locations

  • Hospital de Tortosa Verge de la Cinta

    RECRUITING

    Tortosa, Tarragona, Spain

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