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Efficacy of Peanut Ball Usage on Labor Pain, Support and Control, Anxiety, and Labor Duration

NCT04204395 · Status: COMPLETED · Phase: NA · Type: INTERVENTIONAL · Enrollment: 80

Last updated 2020-10-09

No results posted yet for this study

Summary

\*Primary: To compare the control group, women in the experimental group will have lower level of labor pain after the intervention of peanut ball usage.

\*Secondary: To compare the control group, women in the experimental group will have higher level of support and control after the intervention of peanut ball usage; To compare the control group, women in the experimental group will have lower level of anxiety after intervention of peanut ball usage; To compare the control group, women in the experimental group will have shorter duration of labor after intervention of peanut ball usage.

Conditions

  • Labor Pain

Interventions

DEVICE

Peanut Ball

The participants in the experimental group will use the peanut ball at least every 2 hours, 30-minute usage for each time. More frequency will be available. Then, the participants will stop using the peanut ball when cervical os is dilated and effaced, may be ready to push.

Sponsors & Collaborators

  • Taipei Medical University Hospital

    collaborator OTHER

  • Taipei Medical University

    lead OTHER

Principal Investigators

  • Shu-Yu Kuo, PhD. · Taipei Medical University

Study Design

Allocation
RANDOMIZED
Purpose
SUPPORTIVE_CARE
Masking
SINGLE
Model
PARALLEL

Eligibility

Min Age
20 Years
Sex
FEMALE
Healthy Volunteers
Yes

Timeline & Regulatory

Start
2019-12-25
Primary Completion
2020-06-30
Completion
2020-06-30

Countries

  • Taiwan

Study Locations

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Read the full study record

This page highlights key information. For complete eligibility criteria, study locations, investigator contacts, and the full protocol, visit the original record on ClinicalTrials.gov.

View NCT04204395 on ClinicalTrials.gov