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Weighted blankets tested for pregnancy cramps and anxiety

NCT ID NCT07309016

Symptom relief Sponsor: Ataturk 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 Results may not be published yet.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This status has not been confirmed recently, so it may be out of date.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 looks at whether using a weighted blanket can reduce nighttime leg cramps, improve sleep quality, and lower anxiety and stress in pregnant women. Fifty women in their third trimester will use the blanket for 14 days and compare results to a 14-day period without it. The goal is to find a safe, drug-free way to help pregnant women feel more comfortable and relaxed.

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

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

About 50 people

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

Expected to start

Dec 2025

An estimate. Start dates often move.

Expected to finish

May 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.

Ages

18 to 40 years

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: * Primarily pregnant women between the ages of 18 and 40 , * Low BMI (to be able to use 8kg weighted blanket), * Gestational week ≥ 28, * Third trimester pregnant women, * Singleton pregnancy, * Ability to communicate verbally and in writing in Turkish, * Willingness to participate in research and comply with intervention protocols.. Exclusion Criteria: * Those who have been diagnosed with high-risk pregnancy, * Preeclampsia or eclampsia, placenta previa, * Gestational diabetes requiring insulin, * Diagnosis of fetal growth retardation, * Polyhydramnios or oligohydramnios, asthma , sleep apnea or serious heart/circulatory problems, * History of bleeding during pregnancy, * Obstetric complications requiring close medical monitoring. * Multiple pregnancies, * Previously diagnosed with a sleep disorder, * Having been diagnosed with a psychiatric disorder * Multiparous pregnant women, * Pregnant women in the first two trimesters , * Night shift workers

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Conditions

The condition(s) this trial relates to.

anxiety anxiety disorder Muscle Cramp Sleep-Wake Transition Disorders

As listed by the trial registrant

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

Anxiety Leg cramps, nocturnal Poor sleep quality Pregnancy Stress

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

  • Atatürk University Instiute of Health Sciences, Department of Midwifery

    Erzurum, Lütfen Seçiniz., 25010, Turkey (Türkiye)

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