Actively Recruiting

Phase Not Applicable
Age: 18Years - 35Years
FEMALE
Healthy Volunteers
NCT06436859

The Effect of Stress Ball on Labor Pain, Anxiety and Satisfaction in Labor

Led by Öznur Hayat Öktem · Updated on 2024-05-31

48

Participants Needed

1

Research Sites

52 weeks

Total Duration

On this page

AI-Summary

What this Trial Is About

The aim of this study was to determine the effect of stress ball use during labor on labor pain, anxiety and satisfaction levels in women admitted to Karabük Training and Research Hospital for delivery. H1 Using the Stress Ball in Labor reduces labor pain. H2 Using the Stress Ball in Labor Reduces Anxiety H3 Use of Stress Ball in Labor increases labor satisfaction.

CONDITIONS

Official Title

The Effect of Stress Ball on Labor Pain, Anxiety and Satisfaction in Labor

Who Can Participate

Age: 18Years - 35Years
FEMALE
Healthy Volunteers

Eligibility Criteria

Eligible

You may qualify if you...

  • Being at 38 weeks or more of pregnancy
  • Having a single, healthy fetus in head position
  • Applying during the latent phase of labor (cervical dilatation between 0-3 cm)
  • Planning to give birth vaginally
  • Women aged 18 to 35 years
Not Eligible

You will not qualify if you...

  • Pregnancy through assisted reproductive techniques
  • Having a gestational or chronic disease
  • Having an obstacle to giving birth vaginally
  • Suspicion of fetal anomaly
  • Not volunteering to participate
  • Women under 18 years of age
  • Women who are illiterate in Turkish
  • Decision to perform cesarean section during labor
  • Participant wishes to withdraw from the research
  • Development of fetal distress
  • Use of vacuum or forceps during birth
  • Women with vision, hearing, or mental problems

AI-Screening

AI-Powered Screening

Complete this quick 3-step screening to check your eligibility

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Trial Site Locations

Total: 1 location

1

Karabuk Training and Research Hospital, obstetrics clinic

Karabük, Turkey (Türkiye), 78100

Actively Recruiting

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Research Team

M

Meltem UĞURLU, associate professor

CONTACT

How is the study designed?

Study Type

INTERVENTIONAL

Masking

SINGLE

Allocation

RANDOMIZED

Model

PARALLEL

Primary Purpose

SUPPORTIVE_CARE

Number of Arms

2

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