Breathing Exercises During Labor and Maternal Outcomes
Effects of Breathing Exercises During Labor on Maternal Stress, Satisfaction, and Birth Outcomes: A Randomized Controlled Trial
調査の概要
詳細な説明
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.
研究の種類
入学 (実際)
段階
- 適用できない
連絡先と場所
研究場所
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Istanbul、トルコ(Türkiye)
- Nilgün Avcı
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参加基準
適格基準
就学可能な年齢
- 大人
- 高齢者
健康ボランティアの受け入れ
説明
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
研究計画
研究はどのように設計されていますか?
デザインの詳細
- 主な目的:支持療法
- 割り当て:ランダム化
- 介入モデル:並列代入
- マスキング:なし(オープンラベル)
武器と介入
参加者グループ / アーム |
介入・治療 |
|---|---|
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実験的:Breathing Exercise Group
Participants received guided breathing exercises throughout labor in addition to routine intrapartum care.
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Pregnant women were instructed and guided to perform slow, controlled breathing exercises during each uterine contraction from the latent phase until full cervical dilatation.
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介入なし:Routine Care Group
Participants received routine intrapartum care only.
No breathing exercises were applied.
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この研究は何を測定していますか?
主要な結果の測定
結果測定 |
メジャーの説明 |
時間枠 |
|---|---|---|
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Birth Satisfaction
時間枠:During the fourth stage of labor (within 2 hours after birth).
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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).
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二次結果の測定
結果測定 |
メジャーの説明 |
時間枠 |
|---|---|---|
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Labor Pain Intensity
時間枠:Repeatedly during labor from admission to the labor unit until delivery.
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Pain intensity measured using the Visual Analog Scale (VAS).
Scores range from 0 to 10; higher scores indicate more severe pain.
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Repeatedly during labor from admission to the labor unit until delivery.
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Labor-Related Anxiety
時間枠:During the fourth stage of labor (within 2 hours after birth).
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Anxiety measured using the Oxford Worries About Labour Scale.
Scores range from 10 to 40; higher scores indicate greater anxiety.
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During the fourth stage of labor (within 2 hours after birth).
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Traumatic Birth Perception
時間枠:At admission to the labor unit (baseline) and during the fourth stage of labor (within 2 hours after birth).
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Traumatic birth perception measured using the Traumatic Birth Perception Scale.
Scores range from 0 to 130; higher scores indicate greater traumatic perception.
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At admission to the labor unit (baseline) and during the fourth stage of labor (within 2 hours after birth).
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Fetal Heart Rate During NST
時間枠:During the NST monitoring session (approximately 20 minutes, same visit).
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Fetal heart rate assessed from NST recordings during the monitoring session.
Measured in beats per minute; normal patterns indicate better fetal well-being.
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During the NST monitoring session (approximately 20 minutes, same visit).
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Fetal Movement Count During NST
時間枠:During the NST monitoring session (approximately 20 minutes, same visit).
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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).
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協力者と研究者
スポンサー
研究記録日
主要日程の研究
研究開始 (実際)
一次修了 (実際)
研究の完了 (実際)
試験登録日
最初に提出
QC基準を満たした最初の提出物
最初の投稿 (実際)
学習記録の更新
投稿された最後の更新 (実際)
QC基準を満たした最後の更新が送信されました
最終確認日
詳しくは
この情報は、Web サイト clinicaltrials.gov から変更なしで直接取得したものです。研究の詳細を変更、削除、または更新するリクエストがある場合は、register@clinicaltrials.gov。 までご連絡ください。 clinicaltrials.gov に変更が加えられるとすぐに、ウェブサイトでも自動的に更新されます。