Not yet recruiting NCT07055490
Interdisciplinary Practice Bundle for Second-Stage of Labor and Clinical Outcomes
For patients and families
In plain language
An automatic summary of structured registry data. It is an orientation aid, not a substitute for the official protocol or a physician assessment.
- What is being studied
- The protocol lists: Interdisciplinary Practice Bundle.
- Who it may be relevant to
- Registry conditions: Delivery Outcomes. Basic parameters: 18 years — 36 years · Female.
- What needs checking
- Age, condition and sex are only basic indicators. Prior treatment, laboratory values and other mandatory requirements appear in the eligibility criteria below.
- Where it takes place
- Center list to be confirmed — check the primary protocol.
- Next step
- Save the trial, show it to the treating physician, and confirm current recruitment with the study center. Costs, documents and travel →
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Official title
Effects of an Interdisciplinary Practice Bundle for Second-Stage of Labor on Clinical Outcomes
Overview
This study aims to assess the effect of implementing an interdisciplinary practice bundle during second-stage of labor on clinical outcomes.
Interventions
- Procedure Interdisciplinary Practice Bundle
interdisciplinary practices were combined in a bundle framework called (5-Ps) to maintain normal process during labor and prevent unnecessary routine interventions, which are (patience, positioning, physiological resuscitation, progress, and preventing urinary harm). These practices implemented from the beginning of the second stage of labor which is started from onset of complete cervical dilatation (10 cm) until delivery with a duration of 2 hours period.
Primary outcome measures
- 1- Fatigue Visual Analogue Scale (VAS-F), [Time frame: Study recruitment will take 6 months (from the beggining of July to the end of October, 2025) , all women who admitted to the labor and delivery unit at Mansoura University Hospitals, Egypt, were subjected to eligibility screening.]
- 2- Childbirth Experience Questionnaire (CEQ) [Time frame: Study recruitment will take 6 months (from the beggining of July to the end of October, 2025) , all women who admitted to the labor and delivery unit at Mansoura University Hospitals, Egypt, were subjected to eligibility screening.]
Eligibility criteria
Inclusion criteria
- Primiparous women aged greater than 18 years, with normal pregnancy.
- ≥ 38 weeks of gestation.
- Eligible for normal vaginal delivery
Exclusion criteria
- women with high risk pregnancy.
- Women with medical or psychological disorders.
- Women suspected to cesarean birth.
Criteria are shown verbatim from the registry (in English). Final eligibility is always assessed by the study center.
Healthy volunteers: Yes
Study design
- Allocation
- Randomized
- Model
- Parallel assignment
- Masking
- Open label
- Primary purpose
- Supportive care
Study locations
Center list to be confirmed — check the primary protocol.
Identifiers
NCT: NCT07055490 · IRB. 0591