Using a stress ball during labor to reduce pain and increase comfort
The Effect of the Stress Ball Used in the Active Phase of Labor on Labor Pain and Birth Comfort
This study is testing whether using a stress ball during labor can help pregnant women feel less pain and more comfortable while giving birth.
Quick facts
| Phase | Not applicable |
|---|---|
| Study type | Interventional |
| Enrollment | 140 (estimated) |
| Ages | 18 Years to 40 Years |
| Sex | Female |
| Sponsor | Ataturk University Academic / other |
| Locations | 1 site (Muş, Merkez) |
| Trial ID | NCT06626958 on ClinicalTrials.gov |
What this trial studies
This clinical trial investigates the impact of a stress ball on labor pain and comfort in pregnant women during the active phase of labor. Participants will be monitored from 3-4 cm cervical dilation until 8-9 cm, with one group using the stress ball while the control group receives routine care. The effectiveness of the stress ball will be assessed using the Visual Analog Scale (VAS) to measure pain levels. The goal is to determine if the stress ball can provide significant relief and enhance the birthing experience.
Who should consider this trial
Good fit: Ideal candidates are pregnant women aged 18-40 who are planning a vaginal birth.
Not a fit: Patients with risky pregnancies may not benefit from this study.
Why it matters
Potential benefit: If successful, this approach could offer a simple, non-invasive method to alleviate labor pain and improve comfort for pregnant women.
How similar studies have performed: While the use of stress balls in labor is a relatively novel approach, similar studies have shown positive outcomes with non-pharmacological pain relief methods.
Eligibility criteria
Show full inclusion / exclusion criteria
Inclusion Criteria: * Vaginal birth * Pregnant women between the ages of 18-40 Exclusion Criteria: * Risky pregnancy
Where this trial is running
Muş, Merkez
- Muş State Hospital Birth Hall — Muş, Merkez, Turkey (Türkiye) (Recruiting)
Study contacts
- Principal investigator: Mihriban Elmas — mihriban.elmas@icloud.com
- Study coordinator: Sibel ÖZTÜRK, PhD
- Email: sblsbl0606@gmail.com
- Phone: +90442231
How to participate
- Review the eligibility criteria above with your treating physician.
- Visit the official trial page on ClinicalTrials.gov for the most current contact information and recruitment status.
- Contact the listed study coordinator or principal investigator to request pre-screening. Pre-screening is free and never obligates you to enroll.