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治験 NCT06776263 (DB-PCC)(対象:Post COVID-19 Condition (PCC)、機能不全呼吸、Breathing Pattern Disorder、急性後COVID-19症候群)は募集中です。詳細は治験レーダーのタイル表示と AI 発見ツールで確認するか、ここで質問してください。
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Dysfunctional Breathing in Post COVID-19 Condition. (DB-PCC)

募集中
治験(臨床試験)の詳細は主に英語で提供されています。しかし、治験レーダーAIが支援できます!「治験を説明」をクリックして、選択した言語で試験情報を表示し、議論してください。
治験番号 NCT06776263 (DB-PCC) は 観察研究 臨床試験 で、Post COVID-19 Condition (PCC)、機能不全呼吸、Breathing Pattern Disorder、急性後COVID-19症候群 に関するものです。現在は 募集中 で、2025年1月15日 から開始しています。200 名の参加者 の募集が計画されています。この治験は カロリンスカ研究所 によって主催され、2026年6月30日 に完了予定です。ClinicalTrials.gov からの最新更新日は 2025年2月14日 です。
概要
The goal of this observational study with a cross-sectional design is to investigate what signs, symptoms and assessment which can describe and explain dysfunctional breathing in patients with post COVID-19 condition. The main question aims to answer which measurements can identify and asses dysfunctional breathing in patients with post COVID-19 condition?

Participants for this study will be recruited from the ReCov cohort will be evaluated with diffrent measurments and questionnaires.

詳細説明
The overall aim with the proposed research project is to describe and investigate the underlying mechanisms of dysfunctional breathing and the experience of living with dysfunctional breathing in patients with post-COVID-19 conditions. In addition, validate and evaluate which methods measure dysfunctional breathing regarding content validity, conceptual validity, test-retest reliability, and sensitivity to change for patients with post-COVID-19 conditions. Furthermore, to develop and evaluate an individually adapted intervention with the aim of normalizing the breathing pattern. In the next step, to evaluate the effects of an individually adapted intervention on physical and psychological function and health-related quality of life (HRQoL) in patients with post-COVID-19 conditions, as well as to describe the patients' experiences of rehabilitation.

Methods and planned studies This project is a part of a larger multi-disciplinary and multi-professional study, ReCOV, that takes a holistic perspective on the consequences of the disease. ReCOV is a three-armed project including patients, next of kin and staff (23). Patients have been followed up at the out-patient clinic for patients with PCC at Karolinska University Hospital (K).

The longitudinal observational study is about physical and psychological recovery, objectively measured physical activity and also an interview study of the patients' overall experiences of rehabilitation after COVID-19 both in the acute and long-term perspective. In total approximately 950 patients have accepted to be apart of ReCOV and to this proposed project patients will be recruited from this cohort but also from primary care. This research project will be performed in collaboration with Karolinska Institutet, Karolinska university Hospital (K), Sahlgrenska University Hospital (SH). University of Gothenburg and primary care in Region Stockholm.

Study 1: Dysfunctional breathing in patients with post COVID-19 condition?

Aim: To investigate what signs, symptoms and assessment which can describe and explain dysfunctional breathing in patients with post COVID-19 condition.

Design: Cross-sectional design

Participants: Patients (approximately n=200) for this study will be recruited from the ReCov cohort. All patients will be > 18 years old. Patients that state that they have persistent respiratory problems and abnormal clinical respiratory findings will be included. Patients will also be recruited from primary care if they have suspected dysfunctional breathing pattern (unable to breathe with a normal breathing pattern in standing). Exclusion Criteria: Not able to perform the measurements because of cognitive or physical impairments, ongoing intervention of breathing exercises.

Procedure and outcomes: All included patients will be evaluated for physical and psychological function, symptoms and HrQoL. The following measurements and questionnaires will be used:

Dependent variables (primary outcome):

Health-related Quality of Life (EQ-5D-5L), EQ VAS Breathing pattern by Respiratory Movement Measuring Instrument (RMMI)

Independent, confounding and possible moderating variables:

Inspiratory and expiratory muscle strength (MIP and MEP) (Micro-RPM) Chest mobility by thoracic expansion Six-minute walk to measure endurance (in meters) Spirometry Diaphragmatic ultrasound End tidal CO2 measured during exercise

Physical Activity level (Frändin/ Grimby) Nijmegen questionnaire (dysfunctional breathing) COPD Assessment Test (CAT), questionnaire of symptoms related to breathing and now commonly used for this group of patients Dyspnea (mMRC, Modified Medical Research Council, Dyspnea Scale and BORG CR10) Patient Health Questionnaire (PHQ-9) Generalized Anxiety Disorder 7-item scale (GAD-7) Breathing Pattern Assessment Tool (BPAT)

公式タイトル

Dysfunctional Breathing in Patients With Post COVID-19 Condition

疾患/病気
Post COVID-19 Condition (PCC)機能不全呼吸Breathing Pattern Disorder急性後COVID-19症候群
その他の研究識別子
  • DB-PCC
  • 2024-05930-01
NCT番号
開始日
2025-01-15
最終更新日
2025-02-14
終了予定日
2026-06-30
目標参加者数
200
試験の種類
観察研究
状況
募集中
キーワード
Respiration
Dyspnea
Signs and Symptoms, Respiratory
Hyperventilation
Outcome Assessment, Health Care
Patient Outcome Assessment
Surveys and Questionnaires
群(アーム)/介入
参加グループ/群介入/治療法
Patients with post COVID-19 condition.
Patients with post COVID-19 condition and respiratory problems.
該当なし
主要評価項目
評価指標指標の説明時間枠
Breathing pattern by Respiratory Movement Measuring Instrument (RMMI) and Health-related Quality of Life (EQ-5D-5L)
Will be assesed in a supine position, using the RMMI. First, during 30 seconds of tidal volume breathing. Second, during 60 seconds of performing maximal breathing manoeuvres interspaced by tidal volume breathing and then during 60 seconds after performing activity that triggers dyspnea. The RMMI records bilateral changes in the anterior posterior diameter, including both upper and lower thoracic and abdominal movements. Health-related Quality of Life is measured with EuroQualityOf Life 5 dimensions questionnaire (EQ-5D-5L), which is an instrument that evaluates the generic quality of life. EQ-5D includes a descriptive system, which comprises 5 dimensions of health: mobility, selfcare, usual activities, pain/discomfort, and anxiety/depression. A descriptive index-score between 0-1, higher score indicates higher HRQoL. EQ-5D also includes a visual analog scale (VAS), which records self-rated health status on a graduated (0-100) scale, with higher scores for higher HRQoL
Assessment will be applied only once and takes about 5-10 minutes to be completed.
副次評価項目
評価指標指標の説明時間枠
Maximal Inspiratory Pressure (MIP)
Maximal Inspiratory muscle strength (MIP) will be measured with Micro RPM in cmH2O
Assessment will be applied only once and takes about 5-10 minutes to be completed.
Maximal Expiratory Pressure ( MEP)
Maximal expiratory muscle strength (MEP) will be measured with Micro-RPM in cm H20
Assessment will be applied only once and takes about 5-10 minutes to be completed.
Chest mobility
Chest mobility will be measured with a tape measure at the xiphoid process and the 4th rib
Assessment will be applied only once and takes about 5 minutes to be completed.
Six-minute walk test (6MWT)
Six-minute walk to measure endurance (in meters)
Assessment will be applied only once and takes about 15 minutes to be completed.
Spirometry
Lung function test with forced vital capacity (FVC), forced expiratory flow in one second (FEV1), diffusion capacity (DLCO)
Assessment will be applied only once and takes about 30 minutes to be completed.
End tidal CO2
End tidal CO2 measured during exercise
Assessment will be applied only once and takes about 15 minutes to be completed.
Physical Activity level (Frändin/ Grimby)
Measured with Frändin/Grimby activity scale, which is a self-assessment scale about current levels of physical activity, ranging from 1 to 6. The higher the score, the higher level of physical activity.
Assessment will be applied only once and takes about 2 minutes to be completed.
Nijmegen questionnaire (dysfunctional breathing)
Dysfunctional breathing will be assessed with the Nijmegen questionnaire. The questionnaire consists of 16 items asking about the symptoms related to dysfunctional breathing. Participants will grade how often they suffered from each item on a five-point Likert scale, ranging from 0 to 4, in which 0 is never ,1 is rarely, 2 is sometimes , 3 is often , and 4 is very often. Total score ranging from 0 to 64. A score of 23 and over indicates dysfunctional breathing.
Assessment will be applied only once and takes about 5-10 minutes to be completed.
COPD Assessment Test (CAT)
COPD Assessment Test (CAT), questionnaire of symptoms related to breathing and now commonly used for this group of patients. COPD Total score ranging from 0 to 40, where a higher number indicates more symptoms
Assessment will be applied only once and takes about 5-10 minutes to be completed.
Dyspnea
Dyspnea (mMRC, Modified Medical Research Council 0-4), Dyspnea Scale and BORG CR10). Modified Medical Research Council (mMRC), which is a self-rating tool to measure the degree of disability that breathlessness postures on daily physical activities on a scale from 0 to 4. 0, no breathlessness except on strenuous exercise; 1, shortness of breath when hurrying on the level or walking up a hill; 2, walks slower than people of same age on the level because of breathlessness; 3, stops for breath when walking at their own pace on the level; and 4, Breathless when washing or getting dressed. Borg CR-10 ranging between 0-10. The higher the score, the higher the dyspnea.
Assessment will be applied only once and takes about 5 minutes to be completed.
Depression
Depression will be assessed with the Patient Health Questionnaire (PHQ-9). PHQ-9 which contains 9 items. Total score ranges from 0 to 27. Higher score indicate more severe depression symptoms
Assessment will be applied only once and takes about 5-10 minutes to be completed.
Anxiety
Anxiety will be assessed with the Generalized Anxiety Disorder 7-item scale (GAD-7) which is a self assessment tool. Total score ranging from 0-21. Higher score indicates higher anxiety.
Assessment will be applied only once and takes about 5-10 minutes to be completed.
Breathing Pattern
The Brompton BPAT (BREATHING PATTERN ASSESSMENT TOOL) will be used. Assessment components include (i) evaluation of chest/abdominal wall movement, noise of (ii) inspiratory and (iii) expiratory flow, (iv) channel of inspiration and expiration, (v) signs of air hunger (yawning, sighing and deeper breaths), (vi) RR and (vii) rhythm. Each component is given a score from 0 to 2, based on features consistent with expected normal (0) versus that present in severe dysfunctional breathing (2), giving a total score of between 0 and 14. The BPAT is completed with a patient positioned, as per the standard assessment of resting breathing pattern (i.e. sat comfortably in a supported seat for at least 5 min) and takes approximately 1 min to collate.
Assessment will be applied only once and takes about 5-10 minutes to be completed.
Thickness of the diaphragm
The thickness of the diaphragm will be measured using ultrasound at end-inspiration and end-expiration and is presented in cm.
Assessment will be applied only once and takes about 5-10 minutes to be completed.
Movement of the diaphragm
The movement of the diaphragm at rest, at deep breathing and at sniff manuver will be measured using ultrasound and presented in cm.
Assessment will be applied only once and takes about 5-10 minutes to be completed.
Velocity of the diaphragm
The velocity of the diaphragm movment will be measured with ultra sound and presented as cm/s.
Assessment will be applied only once and takes about 5-10 minutes to be completed.
Thickening fraction of the diaphragm
The thickening fraction of the diaphragm will be measured using ultrasound and is calculated using a formula, thickening fraction=(end-inspiration - end-expration)/ end-expiraton ×100%. Measurements are performed 3 times and the average value is calculated and presented.
Assessment will be applied only once and takes about 5-10 minutes to be completed.
適格基準

対象年齢
成人, 高齢者
試験の最低年齢
18 Years
対象性別
全て
  • Patients that state that they have persistent respiratory problems, have 2 or higher on mMRC scale or 23 and over on the Nijmegen scale will be included.

  • Not able to perform the measurements because of cognitive or physical impairments, ongoing intervention of breathing exercises.
Karolinska Institutet logoカロリンスカ研究所
Karolinska University Hospital logoKarolinska University Hospital
責任者
Malin Nygren-Bonnier, 研究責任者, PhD, Karolinska Institutet
試験中央連絡先
連絡先: Malin Nygren-Bonnier, Associate professor, PhD, +46852488831, [email protected]
2 1カ国の場所

Solna

Karolinska University Hospital, Stockholm, Solna, 17176, Sweden
Malin Nygren Bonnier, PhD, 研究責任者
募集未定
Karolinska Institutet, Huddinge, 14183, Sweden
募集中