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Breathing Exercises During Labor and Maternal Outcomes

30. april 2026 oppdatert av: Nilgun Avci

Effects of Breathing Exercises During Labor on Maternal Stress, Satisfaction, and Birth Outcomes: A Randomized Controlled Trial

This randomized controlled trial evaluated the effects of guided breathing exercises applied during labor on maternal stress, pain, anxiety, birth satisfaction, and labor outcomes. Pregnant women were randomly assigned to a breathing exercise group or a routine care group. Maternal psychological outcomes and labor-related clinical outcomes were compared between groups.

Studieoversikt

Detaljert beskrivelse

Labor is a physiological process that may be accompanied by pain, anxiety, and psychological stress, which can negatively affect birth satisfaction and labor outcomes. Non-pharmacological interventions such as breathing exercises are widely used to support women during labor.

In this randomized controlled experimental study, pregnant women admitted to the labor and delivery unit during the latent phase were randomly assigned to either an experimental group receiving guided breathing exercises throughout labor or a control group receiving routine intrapartum care only. Breathing exercises were applied continuously during uterine contractions until full cervical dilatation.

Maternal pain intensity, anxiety, traumatic birth perception, birth satisfaction, and labor outcomes including labor duration and obstetric interventions were assessed using validated measurement tools. The study aimed to determine whether breathing exercises could improve maternal psychological well-being, enhance birth satisfaction, and positively influence labor outcomes.

Studietype

Intervensjonell

Registrering (Faktiske)

124

Fase

  • Ikke aktuelt

Kontakter og plasseringer

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

Studiesteder

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:

  • Pregnant women admitted to the labor and delivery unit during the latent phase
  • Women planning vaginal birth
  • Volunteered to participate

Exclusion Criteria:

  • Women who did not speak Turkish
  • Women with auditory or mental health problems

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: Breathing Exercise Group
Participants received guided breathing exercises throughout labor in addition to routine intrapartum care.
Pregnant women were instructed and guided to perform slow, controlled breathing exercises during each uterine contraction from the latent phase until full cervical dilatation.
Ingen inngripen: Routine Care Group
Participants received routine intrapartum care only. No breathing exercises were applied.

Hva måler studien?

Primære resultatmål

Resultatmål
Tiltaksbeskrivelse
Tidsramme
Birth Satisfaction
Tidsramme: During the fourth stage of labor (within 2 hours after birth).

Birth satisfaction assessed using the Short Form of the Birth Satisfaction Scale (BSS-R).

Scores range from 0 to 40; higher scores indicate greater satisfaction.

During the fourth stage of labor (within 2 hours after birth).

Sekundære resultatmål

Resultatmål
Tiltaksbeskrivelse
Tidsramme
Labor Pain Intensity
Tidsramme: Repeatedly during labor from admission to the labor unit until delivery.
Pain intensity measured using the Visual Analog Scale (VAS). Scores range from 0 to 10; higher scores indicate more severe pain.
Repeatedly during labor from admission to the labor unit until delivery.
Labor-Related Anxiety
Tidsramme: During the fourth stage of labor (within 2 hours after birth).
Anxiety measured using the Oxford Worries About Labour Scale. Scores range from 10 to 40; higher scores indicate greater anxiety.
During the fourth stage of labor (within 2 hours after birth).
Traumatic Birth Perception
Tidsramme: At admission to the labor unit (baseline) and during the fourth stage of labor (within 2 hours after birth).
Traumatic birth perception measured using the Traumatic Birth Perception Scale. Scores range from 0 to 130; higher scores indicate greater traumatic perception.
At admission to the labor unit (baseline) and during the fourth stage of labor (within 2 hours after birth).
Fetal Heart Rate During NST
Tidsramme: During the NST monitoring session (approximately 20 minutes, same visit).
Fetal heart rate assessed from NST recordings during the monitoring session. Measured in beats per minute; normal patterns indicate better fetal well-being.
During the NST monitoring session (approximately 20 minutes, same visit).
Fetal Movement Count During NST
Tidsramme: During the NST monitoring session (approximately 20 minutes, same visit).

Number of fetal movements recorded by the mother using the event marker during NST monitoring.

Higher counts indicate greater fetal activity.

During the NST monitoring session (approximately 20 minutes, same visit).

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. februar 2021

Primær fullføring (Faktiske)

30. juli 2021

Studiet fullført (Faktiske)

30. juli 2021

Datoer for studieregistrering

Først innsendt

6. februar 2026

Først innsendt som oppfylte QC-kriteriene

30. april 2026

Først lagt ut (Faktiske)

4. mai 2026

Oppdateringer av studieposter

Sist oppdatering lagt ut (Faktiske)

4. 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

Legemiddel- og utstyrsinformasjon, studiedokumenter

Studerer et amerikansk FDA-regulert medikamentprodukt

Nei

Studerer et amerikansk FDA-regulert enhetsprodukt

Nei

Denne informasjonen ble hentet direkte fra nettstedet clinicaltrials.gov uten noen endringer. Hvis du har noen forespørsler om å endre, fjerne eller oppdatere studiedetaljene dine, vennligst kontakt register@clinicaltrials.gov. Så snart en endring er implementert på clinicaltrials.gov, vil denne også bli oppdatert automatisk på nettstedet vårt. .

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