HALOA: Cardiac Coherence With CPAP for Obstructive Sleep Apnea (HALOA)
Effect of Adding Cardiac Coherence to Continuous Positive Airway Pressure in Patients With Obstructive Sleep Apnea: A Multicenter Randomized Delayed-Start Controlled Study
This multicenter study will evaluate whether adding cardiac coherence breathing sessions to continuous positive airway pressure (CPAP) improves sleep quality in adults with newly diagnosed obstructive sleep apnea who are starting CPAP. Approximately 180 participants will be randomly assigned to one of two groups. Both groups will start treatment with the HALOA CPAP system. In one group, the cardiac coherence module will be activated at the start of treatment. In the other group, participants will use CPAP alone for 8 weeks before the module is activated.
Sleep quality will be assessed at study entry, at 8 weeks, and at 16 weeks using the Pittsburgh Sleep Quality Index. The primary comparison will assess the change in sleep quality from study entry to week 8 between the two groups. Secondary assessments will include daytime sleepiness, insomnia symptoms, anxiety and depression symptoms, treatment satisfaction, usability of the cardiac coherence module, CPAP use, and heart-rate variability when polysomnography recordings are available.
調査の概要
状態
詳細な説明
Obstructive sleep apnea is commonly treated with continuous positive airway pressure (CPAP). However, some patients have difficulty adhering to CPAP or experience persistent sleep-related symptoms. Cardiac coherence is a guided breathing practice intended to support relaxation and emotional regulation. The HALOA system combines CPAP treatment with a cardiac coherence module. This study will assess whether access to this module from the start of CPAP treatment improves subjective sleep quality compared with starting the module after an initial period of CPAP alone.
This is a prospective, multicenter, randomized, open-label, delayed-start controlled study. Approximately 180 adults with newly diagnosed obstructive sleep apnea and an indication for CPAP will be enrolled at 11 planned centers. Participants will be randomly assigned in equal numbers to one of two groups.
All participants will begin CPAP treatment using the HALOA system and will receive usual CPAP care. Participants in the immediate-intervention group will have the cardiac coherence module activated at study entry and will receive guidance on its use. Participants in the delayed-intervention group will use CPAP without cardiac coherence for the first 8 weeks. After the week 8 assessment, the module will be activated and participants will receive guidance on its use.
Study assessments will take place at baseline, week 8, and week 16. The primary outcome is the change in the global Pittsburgh Sleep Quality Index (PSQI) score from baseline to week 8, comparing the two randomized groups. The week 8 assessment provides the controlled comparison before participants in the delayed-intervention group begin cardiac coherence. Changes in PSQI from week 8 to week 16 in the delayed-intervention group will also be assessed to explore the effect after the module is introduced.
Secondary assessments will include daytime sleepiness using the Epworth Sleepiness Scale, insomnia symptoms using the Insomnia Severity Index, and anxiety and depression symptoms using the Hospital Anxiety and Depression Scale. Patient satisfaction will be assessed using the CSQ-8 and a study-specific questionnaire. Usability of the cardiac coherence module will be assessed using the System Usability Scale. CPAP adherence will be evaluated using device data, including hours of use and the proportion of participants meeting the protocol-defined adherence threshold. Heart-rate variability indices will be evaluated from polysomnography recordings when available.
Participants will be adults with obstructive sleep apnea diagnosed by polysomnography within the 3 months before inclusion and for whom CPAP treatment is indicated. The protocol lists recent CPAP or mandibular advancement device treatment, refusal of or contraindication to CPAP, inability to use the cardiac coherence device, and specified medical, psychiatric, or other circumstances among the non-inclusion criteria.
研究の種類
入学 (推定)
段階
- 適用できない
連絡先と場所
研究連絡先
- 名前：François FB Bughin, Md, PhD
- 電話番号：0033761783081
- メール：fbughin@hotmail.com
参加基準
適格基準
就学可能な年齢
健康ボランティアの受け入れ
受講資格のある性別
説明
Inclusion Criteria:
- Age 18 years or older.
- Obstructive sleep apnea diagnosed according to ICSD-3 criteria by polysomnography performed within 3 months before study inclusion.
- Indication for CPAP treatment according to current recommendations: apnea-hypopnea index (AHI) ≥30 events/hour, or AHI ≥15 events/hour with severe cardiovascular or respiratory comorbidity.
- Written informed consent.
Exclusion Criteria:
- CPAP or mandibular advancement device treatment within the 3 months before inclusion.
- Refusal of CPAP treatment.
- Contraindication to CPAP treatment.
- Unstable psychiatric disorder or substance-use disorder.
- Technical inability to use the cardiac coherence device.
- Not affiliated with, or not a beneficiary of, a social security system.
- Deprivation of liberty by judicial or administrative decision.
- Legal protective measure, including guardianship or curatorship.
- Pregnancy, childbirth, or breastfeeding.
- Language barrier preventing participation.
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：処理
- 割り当て：ランダム化
- 介入モデル：並列代入
- マスキング：独身
武器と介入
参加者グループ / アーム |
介入・治療 |
|---|---|
|
実験的：Immediate cardiac coherence with CPAP
Participants will start HALOA CPAP at study inclusion. The cardiac coherence breathing module will be activated from the start of treatment, with guidance on its use. Participants will be assessed at baseline, week 8, and week 16. |
CPAP treatment using the HALOA system, initiated at study inclusion in both groups and provided as part of usual care. Guided cardiac coherence breathing sessions using the module integrated with the HALOA system. The module is activated at study inclusion in the experimental group and after the week 8 assessment in the active comparator group. |
|
アクティブコンパレータ：Delayed cardiac coherence with CPAP
Participants will start HALOA CPAP at study inclusion and use it without the cardiac coherence module for 8 weeks. After the week 8 assessment, the module will be activated and guidance on its use provided. Participants will be assessed at baseline, week 8, and week 16. |
CPAP treatment using the HALOA system, initiated at study inclusion in both groups and provided as part of usual care. |
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 |
|---|---|---|
|
Change in Global Pittsburgh Sleep Quality Index (PSQI) Score
時間枠：Baseline to week 8
|
Absolute change in the global PSQI score from baseline (V1) to week 8 (V2), comparing the randomized groups. PSQI scores range from 0 to 21; higher scores indicate poorer sleep quality. |
Baseline to week 8
|
二次結果の測定
結果測定 |
メジャーの説明 |
時間枠 |
|---|---|---|
|
Change in PSQI Score After Delayed Initiation of Cardiac Coherence
時間枠：Week 8 to week 16
|
Absolute change in global PSQI score from week 8 (V2) to week 16 (V3) in the delayed-intervention group, after the cardiac coherence module is activated. |
Week 8 to week 16
|
|
Change in Daytime Sleepiness
時間枠：Baseline, week 8, and week 16
|
Changes in Epworth Sleepiness Scale (ESS) |
Baseline, week 8, and week 16
|
|
Change in insomnia symptoms
時間枠：Baseline, week 8, and week 16
|
Changes in Insomnia Severity Index (ISI) |
Baseline, week 8, and week 16
|
|
Change in depression symptoms
時間枠：Baseline, week 8, and week 16
|
Changes in Hospital Anxiety and Depression Scale anxiety and depression subscale scores (HADS-A and HADS-D). |
Baseline, week 8, and week 16
|
|
Patient Satisfaction
時間枠：Baseline, week 8, and week 16, as applicable
|
Patient satisfaction measured using the Client Satisfaction Questionnaire (CSQ-8) and the study-specific S-HALOA-CC questionnaire. S-HALOA-CC results will be considered exploratory. |
Baseline, week 8, and week 16, as applicable
|
|
Usability of the Cardiac Coherence Module
時間枠：Week 8 for the immediate-intervention group and week 16 for the delayed-intervention group
|
Usability measured using the System Usability Scale (SUS) after exposure to the cardiac coherence module. |
Week 8 for the immediate-intervention group and week 16 for the delayed-intervention group
|
|
CPAP Adherence
時間枠：At weeks 8 and 16; device use assessed over the 7-day and 30-day periods before each visit
|
Mean nightly CPAP use and the proportion of participants meeting the protocol-defined adherence threshold of at least 4 hours per night on at least 70% of nights. |
At weeks 8 and 16; device use assessed over the 7-day and 30-day periods before each visit
|
|
Heart-Rate Variability
時間枠：Baseline and week 16, when recordings are available
|
Changes in time-domain and frequency-domain heart-rate variability indices derived from polysomnography recordings, when follow-up recordings are available. |
Baseline and week 16, when recordings are available
|
|
Clinically Meaningful Improvement in Sleep Quality
時間枠：Baseline to week 8, week 8 to week 16, and baseline to week 16
|
Proportion of participants with a decrease of at least 3 points in global PSQI score over the specified assessment interval. |
Baseline to week 8, week 8 to week 16, and baseline to week 16
|
協力者と研究者
スポンサー
出版物と役立つリンク
一般刊行物
- Herhaus B, Kalin A, Gouveris H, Petrowski K. Mobile Heart Rate Variability Biofeedback Improves Autonomic Activation and Subjective Sleep Quality of Healthy Adults - A Pilot Study. Front Physiol. 2022 Feb 17;13:821741. doi: 10.3389/fphys.2022.821741. eCollection 2022.
- Laborde S, Hosang T, Mosley E, Dosseville F. Influence of a 30-Day Slow-Paced Breathing Intervention Compared to Social Media Use on Subjective Sleep Quality and Cardiac Vagal Activity. J Clin Med. 2019 Feb 6;8(2):193. doi: 10.3390/jcm8020193.
- Stepnowsky C, Zamora T, Edwards C. Does Positive Airway Pressure Therapy Result in Improved Sleep Quality? Health (Irvine Calif). 2014 Oct;6(18):2416-2424. doi: 10.4236/health.2014.618278.
研究記録日
主要日程の研究
研究開始 (推定)
一次修了 (推定)
研究の完了 (推定)
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
本研究に関する用語
追加の関連 MeSH 用語
その他の研究ID番号
- 26.01725.000477
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?
IPD プランの説明
The sponsor has not yet determined whether individual participant data and the corresponding data dictionary will be made available to other researchers. The plan will be updated once a decision has been made.
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
米国FDA規制機器製品の研究
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