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Diaphragmatic and Box Breathing on Heart Rate Variability and Perceived Stress (HRV DB BB PSS)

2026年7月13日 更新者:Alaa Naseer Abdelhameed Abdelmohsen、Cairo University

Enhancing Physiological and Psychological Resilience: A Comparative Study of Diaphragmatic and Box Breathing in Physical Therapy Students.

The goal of this clinical trial is to learn if diaphragmatic breathing and box breathing work to enhance resilience and manage stress in physical therapy students. It will also learn about their effects on overall physiological and psychological parameters. The main questions it aims to answer are:

Do these breathing techniques improve heart rate variability (HRV)?

How do these interventions affect participants' perceived stress levels, cognitive performance, and academic achievement?

Researchers will compare diaphragmatic breathing and box breathing to a control group to see if these non-invasive methods work to improve physiological adaptation and manage stress.

Participants will:

Be randomly assigned to practice diaphragmatic breathing, practice box breathing, or join a control group Have their heart rate variability (HRV) measured as a primary sign of physiological adaptation Complete assessments to evaluate their perceived stress, cognitive performance, and academic achievement

調査の概要

詳細な説明

The Challenge: Stress in Healthcare Education University life is a demanding transitional period, and students training in healthcare fields like physical therapy often face immense academic and clinical pressures. Research shows that up to 50.1% of physiotherapy students experience high levels of stress, which can surge even higher during their hands-on clinical rotations. This stress is more than just an emotional burden; it actively impairs working memory, reduces attention span, and often leads to lower grades and poorer overall academic performance.

The Goal of the Study This study aims to discover if simple, accessible breathing exercises can help undergraduate physical therapy students build resilience and better manage their stress. Specifically, the research will compare the effectiveness of two distinct breathing techniques-diaphragmatic breathing and box breathing-to see how they impact both the mind (psychological stress and cognition) and the body (physiological adaptation).

How the Study Works The study will involve 60 undergraduate physical therapy students from Deraya University who are currently experiencing moderate to high levels of academic stress. These participants will be randomly divided into three equal groups: The Diaphragmatic Breathing Group: Participants will practice a relaxing, slow-paced breathing pattern. They will inhale through the nose for 4 seconds and exhale through the mouth for 6 seconds, focusing on expanding their abdomen. The Box Breathing Group: Participants will practice a structured technique often used in high-stress tactical environments to enhance stress tolerance. It involves a "4-4-4-4" cycle: inhaling for 4 seconds, holding the breath for 4 seconds, exhaling for 4 seconds, and holding the breath out for 4 seconds. The Control Group: Participants will simply continue their normal daily routines without any specific breathing interventions so researchers have a baseline for comparison. The two breathing groups will practice their designated techniques for 15 minutes a day, 6 days a week, over a 4-week period. What is Being Measured?To accurately determine if these techniques work, the study will evaluate several key areas:Heart Rate Variability (HRV): Using a highly accurate chest strap sensor (the Polar H10), researchers will measure the subtle variations in time between heartbeats. HRV is a primary indicator of how well the nervous system is regulating stress and keeping the body balanced. Stress and Resilience: Participants will complete standardized questionnaires to evaluate their perceived stress levels and their ability to "bounce back" from daily challenges. Cognitive and Academic Performance: The study will use specialized cognitive tests (like the Stroop Color-Word Test) to measure attention and executive functioning. It will also evaluate the students' confidence in their ability to manage time, prepare for exams, and succeed academically.

Why This Matters Because academic stress is incredibly prevalent among health sciences students, finding practical, non-medication-based ways to support their mental health is critical. By comparing these two breathing methods, this study hopes to identify an effective, non-invasive tool that students can easily use to lower their anxiety, improve their focus, and ultimately thrive in their demanding academic and clinical environments.

研究の種類

介入

入学 (推定)

60

段階

  • 適用できない

連絡先と場所

このセクションには、調査を実施する担当者の連絡先の詳細と、この調査が実施されている場所に関する情報が記載されています。

研究連絡先

  • 名前:Alaa N Abdelhameed Abdelmohsen, B.Sc. in Physical Therapy
  • 電話番号:+201061382864
  • メールalaa.nasser@deraya.edu.eg

研究連絡先のバックアップ

研究場所

    • Minya Province
      • Minya、Minya Province、エジプト
        • Faculty of Physical Therapy, Deraya University
        • コンタクト:

参加基準

研究者は、適格基準と呼ばれる特定の説明に適合する人を探します。これらの基準のいくつかの例は、人の一般的な健康状態または以前の治療です。

適格基準

就学可能な年齢

  • 大人

健康ボランティアの受け入れ

はい

説明

Inclusion Criteria:

  • Academic Status: Currently enrolled, full-time undergraduate Physical Therapy students
  • Age Range: 18-25 years
  • Health Status: Generally healthy individuals with no known chronic respiratory or cardiovascular diseases.
  • Informed Consent: Ability and willingness to provide written informed consent and commit to the 4-week protocol (6 sessions/week).
  • Stress Level: A baseline score on the Perceived Stress Scale (PSS) indicating at least moderate stress.

Exclusion Criteria:

  • Pre-existing Breathing Expertise: Individuals with professional training in yoga (Pranayama), formal meditation, or advanced breath work that might bias the baseline results.
  • Medical Conditions: Diagnosed respiratory conditions (e.g., Asthma, COPD).
  • Cardiovascular issues (e.g., Arrhythmias, Hypertension).
  • Clinical psychological disorders (e.g., Generalized Anxiety Disorder or Panic Disorder) that may require medication.
  • Pharmacological Factors: Use of medications that influence the Autonomic Nervous System (e.g., Beta-blockers, antidepressants, or heavy use of stimulants/sedatives).
  • Substance Use: Smokers/Vapers
  • Excessive Caffeine "Participants consuming more than 400 mg of caffeine per day (equivalent to approximately 4 standard cups of brewed coffee) will be excluded.
  • Recent Acute Illness: Any respiratory tract infection or fever within two weeks prior to the start of the study

研究計画

このセクションでは、研究がどのように設計され、研究が何を測定しているかなど、研究計画の詳細を提供します。

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
実験的:Diaphragmatic Breathing Group

Participants will sit comfortably with their hands in their abdomen. They will:

  • Inhale through the nose for 4 seconds
  • Exhale through the mouth for 6 seconds
  • Focus on abdominal expansion and relaxation
  • Continue for 15 minutes, 6 sessions/week, for 4 weeks

Diaphragmatic Breathing Group:

Participants will sit comfortably with their hands in their abdomen. They will:

  • Inhale through the nose for 4 seconds
  • Exhale through the mouth for 6 seconds
  • Focus on abdominal expansion and relaxation
  • Continue for 15 minutes, 6 sessions/week, for 4 weeks
実験的:Box Breathing Group

Participants will perform a structured breath cycle:

  • Inhale for 4 seconds
  • Hold for 4 seconds
  • Exhale for 4 seconds
  • Hold for 4 seconds Sessions will last 15 minutes, 6 sessions/week, for 4 weeks

Box Breathing Group:

Participants will perform a structured breath cycle:

  • Inhale for 4 seconds
  • Hold for 4 seconds
  • Exhale for 4 seconds
  • Hold for 4 seconds
介入なし:Control Group
Participants will continue their normal daily routines and will not receive any breathing intervention during the study period

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
Heart Rate Variability
時間枠:Baseline (pre-intervention) and at the end of the 4-week training period (post-intervention).
HRV will be measured using the Polar H10 sensor and analyzed through Kubios HRV software to evaluate physiological resilience and autonomic nervous system regulation.
Baseline (pre-intervention) and at the end of the 4-week training period (post-intervention).
Perceived Stress
時間枠:Baseline (pre-intervention) and at the end of the 4-week training period (post-intervention).
Stress will be measured using the Perceived Stress Scale (PSS-10). The total score ranges from a minimum of 0 to a maximum of 40. Higher scores indicate higher levels of perceived stress, representing a worse outcome
Baseline (pre-intervention) and at the end of the 4-week training period (post-intervention).
Resilience
時間枠:Baseline (pre-intervention) and at the end of the 4-week training period (post-intervention).
Resilience will be measured using the Brief Resilience Scale (BRS). The score ranges from a minimum of 1 to a maximum of 5. Higher scores indicate higher levels of resilience, representing a better outcome
Baseline (pre-intervention) and at the end of the 4-week training period (post-intervention).

二次結果の測定

結果測定
メジャーの説明
時間枠
Cognitive Performance
時間枠:Baseline (pre-intervention) and at the end of the 4-week training period (post-intervention).
Cognitive performance will be assessed using the Stroop Color-Word Test. The score represents the number of correct responses. The minimum possible score is 0, with no strictly defined maximum. Higher scores indicate better cognitive performance, representing a better outcome
Baseline (pre-intervention) and at the end of the 4-week training period (post-intervention).
Academic Achievement
時間枠:Baseline (pre-intervention) and at the end of the 4-week training period (post-intervention).
Academic achievement will be assessed using the 9-item Academic Self-Efficacy Scale (ASE). The total score ranges from a minimum of 9 to a maximum of 63. Higher scores indicate higher levels of academic self-efficacy, representing a better outcome
Baseline (pre-intervention) and at the end of the 4-week training period (post-intervention).

協力者と研究者

ここでは、この調査に関係する人々や組織を見つけることができます。

スポンサー

捜査官

  • スタディチェア:Rana H Elbanaa, Assoiate Professor、Cairo University
  • スタディディレクター:Fatma Y Abdelsalam, Lecturer、Cairo University

研究記録日

これらの日付は、ClinicalTrials.gov への研究記録と要約結果の提出の進捗状況を追跡します。研究記録と報告された結果は、国立医学図書館 (NLM) によって審査され、公開 Web サイトに掲載される前に、特定の品質管理基準を満たしていることが確認されます。

主要日程の研究

研究開始 (推定)

2026年7月1日

一次修了 (推定)

2026年12月30日

研究の完了 (推定)

2027年3月1日

試験登録日

最初に提出

2026年7月7日

QC基準を満たした最初の提出物

2026年7月7日

最初の投稿 (実際)

2026年7月13日

学習記録の更新

投稿された最後の更新 (実際)

2026年7月14日

QC基準を満たした最後の更新が送信されました

2026年7月13日

最終確認日

2026年7月1日

詳しくは

本研究に関する用語

その他の研究ID番号

  • CU-AN-19052026

個々の参加者データ (IPD) の計画

個々の参加者データ (IPD) を共有する予定はありますか?

いいえ

IPD プランの説明

Individual participant data will not be shared to maintain participant privacy and strictly adhere to confidentiality agreements.

医薬品およびデバイス情報、研究文書

米国FDA規制医薬品の研究

いいえ

米国FDA規制機器製品の研究

いいえ

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。

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