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Showering During Labor

30. april 2026 oppdatert av: Nilgun Avci

Effects of Showering During Labor on Pain, Anxiety, Comfort, Satisfaction, and Labor Outcomes: A Randomized Controlled Trial

This study examined whether showering during labor affects pain, anxiety, comfort, satisfaction, and labor outcomes in women undergoing vaginal birth. Non-pharmacological methods are commonly used to support women during labor, and warm showering may help reduce discomfort and emotional distress during the labor process.

In this randomized controlled trial, pregnant women in active labor were assigned either to a shower group or to a control group receiving routine labor care. Women in the shower group were allowed to shower during labor under standardized conditions, while the control group received routine intrapartum care without showering. Pain and anxiety levels were assessed repeatedly during labor, while comfort and birth satisfaction were evaluated during and after birth using validated measurement tools.

The results of this study aim to contribute to evidence-based intrapartum care practices by evaluating the role of showering as a supportive intervention during labor.

Studieoversikt

Status

Fullført

Forhold

Intervensjon / Behandling

Studietype

Intervensjonell

Registrering (Faktiske)

94

Fase

  • Ikke aktuelt

Kontakter og plasseringer

Denne delen inneholder kontaktinformasjon for de som utfører studien, og informasjon om hvor denne studien blir utført.

Studiesteder

    • Istanbul
      • Istanbul, Istanbul, Tyrkia (Türkiye), 34010
        • State Obstetrics and Gynecology Hospital, Istanbul

Deltakelseskriterier

Forskere ser etter personer som passer til en bestemt beskrivelse, kalt kvalifikasjonskriterier. Noen eksempler på disse kriteriene er en persons generelle helsetilstand eller tidligere behandlinger.

Kvalifikasjonskriterier

Alder som er kvalifisert for studier

  • Voksen
  • Eldre voksen

Tar imot friske frivillige

Ja

Beskrivelse

Inclusion Criteria:

  • Women admitted to the labor unit during the study period
  • Term pregnancy (37-41 weeks)
  • Planned vaginal birth
  • Cervical dilation greater than 5 cm
  • Volunteered to participate and provided informed consent

Exclusion Criteria:

  • Inability to communicate in Turkish
  • Hearing or mental health conditions
  • Conversion from vaginal birth to cesarean section
  • Age under 18 years
  • High-risk pregnancy (e.g., preeclampsia, diabetes, hypertension, multiple pregnancy, placental abnormalities)
  • Use of epidural anesthesia

Studieplan

Denne delen gir detaljer om studieplanen, inkludert hvordan studien er utformet og hva studien måler.

Hvordan er studiet utformet?

Designdetaljer

  • Primært formål: Støttende omsorg
  • Tildeling: Randomisert
  • Intervensjonsmodell: Parallell tildeling
  • Masking: Ingen (Open Label)

Våpen og intervensjoner

Deltakergruppe / Arm
Intervensjon / Behandling
Eksperimentell: Shower During Labor
Participants were allowed to shower during active labor (cervical dilation >5 cm) in a private bathroom within the labor room. Showering was permitted at the participant's preference, for at least 20 minutes per session, with water temperature maintained between 35-40°C. Safety measures were implemented, including accompaniment by a companion or researcher.
Participants were allowed to shower during active labor (cervical dilation >5 cm) in a private bathroom within the labor room. Showering was permitted at the participant's preference, for at least 20 minutes per session, with water temperature maintained between 35-40°C. Safety measures were implemented, including accompaniment by a companion or researcher.
Ingen inngripen: Control: Routine Labor Care
Participants received routine intrapartum care without showering during labor.

Hva måler studien?

Primære resultatmål

Resultatmål
Tiltaksbeskrivelse
Tidsramme
Labor Pain Intensity
Tidsramme: Every 2 hours during labor (up to 8 hours) and immediately before and after each shower session during the same labor admission.
Pain intensity assessed using the Visual Analog Scale (VAS) during labor.
Every 2 hours during labor (up to 8 hours) and immediately before and after each shower session during the same labor admission.

Sekundære resultatmål

Resultatmål
Tiltaksbeskrivelse
Tidsramme
Anxiety Level During Labor
Tidsramme: Every 2 hours during labor (up to 8 hours) and immediately before and after each shower session during the same labor admission.
Anxiety assessed using the Visual Analog Scale (VAS) during labor.
Every 2 hours during labor (up to 8 hours) and immediately before and after each shower session during the same labor admission.
Maternal Comfort During Labor
Tidsramme: At 10 minutes after the first shower session during active labor
Maternal comfort assessed using the Childbirth Comfort Questionnaire.
At 10 minutes after the first shower session during active labor
Birth Satisfaction
Tidsramme: 2 hours postpartum.
Birth satisfaction assessed using the Birth Satisfaction Scale.
2 hours postpartum.
Duration of Labor
Tidsramme: From admission to the labor unit until delivery.
Total duration of labor measured in hours, obtained from clinical records.
From admission to the labor unit until delivery.
Mode of Delivery
Tidsramme: At delivery.
Type of delivery (vaginal or cesarean) recorded from clinical records.
At delivery.
Use of Obstetric Interventions
Tidsramme: During labor and recorded at delivery.
Use of obstetric interventions (e.g., induction, augmentation, episiotomy) recorded from clinical records.
During labor and recorded at delivery.

Samarbeidspartnere og etterforskere

Det er her du vil finne personer og organisasjoner som er involvert i denne studien.

Sponsor

Studierekorddatoer

Disse datoene sporer fremdriften for innsending av studieposter og sammendragsresultater til ClinicalTrials.gov. Studieposter og rapporterte resultater gjennomgås av National Library of Medicine (NLM) for å sikre at de oppfyller spesifikke kvalitetskontrollstandarder før de legges ut på det offentlige nettstedet.

Studer hoveddatoer

Studiestart (Faktiske)

1. mars 2022

Primær fullføring (Faktiske)

30. august 2022

Studiet fullført (Faktiske)

30. august 2022

Datoer for studieregistrering

Først innsendt

6. februar 2026

Først innsendt som oppfylte QC-kriteriene

30. april 2026

Først lagt ut (Faktiske)

6. mai 2026

Oppdateringer av studieposter

Sist oppdatering lagt ut (Faktiske)

6. mai 2026

Siste oppdatering sendt inn som oppfylte QC-kriteriene

30. april 2026

Sist bekreftet

1. april 2026

Mer informasjon

Begreper knyttet til denne studien

Andre studie-ID-numre

  • Showering During Labor

Legemiddel- og utstyrsinformasjon, studiedokumenter

Studerer et amerikansk FDA-regulert medikamentprodukt

Nei

Studerer et amerikansk FDA-regulert enhetsprodukt

Nei

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