Cette page a été traduite automatiquement et l'exactitude de la traduction n'est pas garantie. Veuillez vous référer au version anglaise pour un texte source.

Investigation of the Effect of Inspiratory Muscle Training and Dual-Task Inspiratory Muscle Training on Cognitive Functions in Heart Failure

29 juillet 2026 mis à jour par: Vildan Fidanoglu, Istanbul University - Cerrahpasa

The goal of this clinical trial is to evaluate whether dual-task inspiratory muscle training (IMT) is effective in improving cognitive and functional outcomes in adults with heart failure. It will also assess the effects of standard IMT and compare both approaches.

The main questions it aims to answer are:

  • Does dual-task IMT improve cognitive function more than standard IMT or no intervention?
  • Does dual-task IMT improve respiratory function, inspiratory muscle strength, and exercise capacity?
  • What are the effects of dual-task IMT on symptoms such as dyspnea and fatigue, and on quality of life, anxiety, and depression?

Dual-task IMT, standard IMT, and a control group (no additional intervention) will be compared to determine which approach is more effective in patients with heart failure (HF).

Participants will:

  • Be randomly assigned to one of three groups: dual-task IMT, standard IMT, or control
  • Perform IMT training 5 days per week for 8 weeks (2 sessions per day, 15 minutes each) if assigned to an intervention group
  • Complete 1 supervised in-person session per week and 4 sessions via telerehabilitation if assigned to an intervention group
  • Undergo assessments before and after the 8-week intervention, including cognitive tests, respiratory function, exercise capacity, and symptom evaluations

Aperçu de l'étude

Statut

Recrutement

Les conditions

Intervention / Traitement

Description détaillée

HF is a complex clinical syndrome associated with reduced functional capacity and a high prevalence of cognitive impairment, which negatively affects prognosis and quality of life. Inspiratory muscle weakness is also common in HF and is associated with increased dyspnea and reduced exercise tolerance. The IMT has been shown to improve respiratory and functional outcomes; however, its effects on cognitive function remain unclear. Dual-task approaches, involving the simultaneous performance of motor and cognitive tasks, have been suggested to enhance neurocognitive integration and improve both cognitive and functional performance. Despite this, the effects of IMT applied within a motor-cognitive dual-task framework in HF patients have not been sufficiently investigated. This study is designed as a prospective, randomized controlled, single-blind trial. A total of 54 patients with heart failure will be included and randomly assigned to three groups: control, standard IMT, and dual-task IMT. Both intervention groups will receive IMT at 50% of maximal inspiratory pressure (MIP) for 8 weeks, 5 days per week, 2 sessions per day (15 minutes each). One session per week will be supervised, and the remaining sessions will be conducted via telerehabilitation (4 days/week, 2 sessions per day). Training intensity will be adjusted weekly. In the dual-task IMT group, cognitive tasks targeting attention, memory, and executive functions will be performed simultaneously with IMT. Assessments will be performed before and after the intervention. Primary outcomes will include cognitive function, while secondary outcomes will include respiratory function, inspiratory muscle strength and endurance, exercise capacity, dyspnea, fatigue, nitric oxide levels, frailty, physical performance, quality of life, and psychological status. This study aims to determine the effectiveness of dual-task IMT compared to standard IMT and control conditions, and to provide evidence for integrated rehabilitation approaches in patients with HF.

Type d'étude

Interventionnel

Inscription (Estimé)

54

Phase

  • N'est pas applicable

Contacts et emplacements

Cette section fournit les coordonnées de ceux qui mènent l'étude et des informations sur le lieu où cette étude est menée.

Coordonnées de l'étude

Lieux d'étude

  • Turquie (Türkiye)
    • Fatih
      • Istanbul, Fatih, Turquie (Türkiye), 34098
        • Recrutement
        • Istanbul University-Cerrahpaşa, Cardiology Institute
        • Contact:

Critères de participation

Les chercheurs recherchent des personnes qui correspondent à une certaine description, appelée critères d'éligibilité. Certains exemples de ces critères sont l'état de santé général d'une personne ou des traitements antérieurs.

Critère d'éligibilité

Âges éligibles pour étudier

  • Adulte
  • Adulte plus âgé

Accepte les volontaires sains

Non

La description

Inclusion Criteria:

  • Age ≥ 40 years
  • Diagnosed with HF with reduced ejection fraction (HFrEF) according to the 2023 ESC HF Guidelines
  • Classified as NYHA functional class I-III
  • Clinically stable for at least 3 months and receiving stable pharmacological treatment
  • Able to read and understand Turkish
  • MoCA score ≥ 21
  • Willingness to participate and provide written informed consent

Exclusion Criteria:

  • Diagnosis of any neurological or neurodegenerative disease (e.g., Parkinson's disease, stroke, dementia, Alzheimer's disease)
  • Diagnosis of pulmonary disease (e.g., chronic obstructive pulmonary disease, obstructive sleep apnea)
  • Myocardial infarction within the last 6 months
  • Uncontrolled hypertension and/or diabetes mellitus
  • Severe valvular heart disease and/or uncontrolled arrhythmias
  • Orthopedic, visual, or hearing impairments that may prevent independent test completion
  • Inability to comply with study procedures or follow instructions

Plan d'étude

Cette section fournit des détails sur le plan d'étude, y compris la façon dont l'étude est conçue et ce que l'étude mesure.

Comment l'étude est-elle conçue ?

Détails de conception

  • Objectif principal: Traitement
  • Répartition: Randomisé
  • Modèle interventionnel: Affectation parallèle
  • Masquage: Aucun (étiquette ouverte)

Armes et Interventions

Groupe de participants / Bras
Intervention / Traitement
Expérimental: Dual-Task IMT
Participants will receive IMT combined with simultaneous cognitive tasks for 8 weeks (5 days/week, 2 sessions/day). One session per week will be supervised, and the remaining sessions will be performed via telerehabilitation. Training intensity will be set at 50% of MIP and adjusted weekly.
Comportemental: Dual-Task IMT
IMT will be applied using a threshold loading device at 50% of MIP for 8 weeks (5 days/week, 2 sessions/day, 15 minutes each). One session per week will be supervised, and the remaining sessions will be performed via telerehabilitation. During IMT, participants will simultaneously perform cognitive tasks targeting attention, memory, and executive functions, which will be varied weekly to minimize learning effects.
Autres noms:
  • Cognitive-Motor IMT
  • Cognitive-Motor Dual-Task
  • Dual-Task
Expérimental: Standard IMT
Participants will receive IMT alone for 8 weeks (5 days/week, 2 sessions/day). One session per week will be supervised, and the remaining sessions will be performed via telerehabilitation. Training intensity will be set at 50% of MIP and adjusted weekly.
Comportemental: IMT
IMT will be applied using a threshold loading device at 50% of MIP for 8 weeks (5 days/week, 2 sessions/day, 15 minutes each). One session per week will be supervised, and the remaining sessions will be performed via telerehabilitation. No additional cognitive task will be applied during training.
Autres noms:
  • Entraînement des muscles inspiratoires
Aucune intervention: Control (Usual Care)
Participants will not receive any additional intervention and will continue their usual medical care. Assessments will be performed at baseline and after 8 weeks.

Que mesure l'étude ?

Principaux critères de jugement

Mesure des résultats
Description de la mesure
Délai
Global cognitive function
Délai: Baseline and 8 weeks (post-intervention)
Global cognitive function will be assessed using the Montreal Cognitive Assessment (MoCA), 0-30 point screening tool evaluating multiple cognitive domains including attention, memory, executive functions, visuospatial abilities, and language. Higher scores indicate better cognitive performance. The assessment will be administered by a certified physiotherapist.
Baseline and 8 weeks (post-intervention)
Subjective cognitive function
Délai: Baseline and 8 weeks (post-intervention)
Subjective cognitive function will be assessed using the Cognitive Failures Questionnaire (CFQ), which evaluates perceived cognitive performance over the past 6 months. The questionnaire consists of 25 items rated on a 5-point Likert scale (0-4), with total scores ranging from 0 to 100. Higher scores indicate greater perceived cognitive impairment.
Baseline and 8 weeks (post-intervention)
Attention and executive function
Délai: Baseline and 8 weeks (post-intervention)
Attention and executive function will be assessed using a Stroop Test (The Scientific and Technological Research Council of Türkiye, Basic Sciences Research Group version), a standardized tool evaluating selective attention, cognitive flexibility, and psychomotor speed. The test consists of five sections, and completion time, as well as the number of correct and incorrect responses, will be recorded for each section. Longer completion times and higher error rates indicate poorer performance.
Baseline and 8 weeks (post-intervention)
Verbal memory
Délai: Baseline and 8 weeks (post-intervention)
Verbal memory will be assessed using the Öktem Verbal Memory Processes Test, which evaluates different components of verbal memory including learning, delayed recall, and recognition. The test involves repeated presentation of a target word list, followed by delayed recall and recognition tasks. Performance will be quantified using learning, spontaneous recall, and recognition scores. The learning score reflects total words recalled across repeated trials (maximum 15). Spontaneous recall is assessed approximately 40 minutes after the learning phase, during which participants are asked to recall the words without cueing. Recognition performance is based on identifying previously presented words among distractors. Higher scores indicate better verbal memory performance.
Baseline and 8 weeks (post-intervention)
Reaction time
Délai: Baseline and 8 weeks (post-intervention)
Reaction time will be assessed using a BlazePod reaction kits. Participants, seated in front of a table, will respond to randomly illuminated light stimuli by tapping the lights as quickly as possible for 30 seconds using one hand. The system consists of four reaction pods positioned in a straight line at 20 cm intervals. Outcome measures will include total number of hits, total reaction time, and mean reaction time per stimulus. Missed responses will be recorded when the light deactivates before being tapped within 4 seconds. Lower reaction time indicates better performance.
Baseline and 8 weeks (post-intervention)

Mesures de résultats secondaires

Mesure des résultats
Description de la mesure
Délai
Forced vital capacity
Délai: Baseline and 8 weeks (post-intervention)
Forced vital capacity (FVC) will be assessed using spirometry according to American Thoracic Society/European Respiratory Society (ATS/ERS) guidelines. It will be recorded from three acceptable maneuvers performed in a seated position, and the highest value will be used for analysis.
Baseline and 8 weeks (post-intervention)
Forced expiratory volume in 1 second (FEV1)
Délai: Baseline and 8 weeks (post-intervention)
Forced expiratory volume in 1 second (FEV1) will be assessed using spirometry according to ATS/ERS guidelines. It will be recorded from three acceptable maneuvers performed in a seated position, and the highest value will be used for analysis.
Baseline and 8 weeks (post-intervention)
FEV1/FVC
Délai: Baseline and 8 weeks (post-intervention)
FEV1/FVC ratio will be assessed using spirometry according to ATS/ERS guidelines. It will be recorded from three acceptable maneuvers performed in a seated position, and the highest value will be used for analysis.
Baseline and 8 weeks (post-intervention)
Peak expiratory flow
Délai: Baseline and 8 weeks (post-intervention)
Peak expiratory flow (PEF) will be assessed using spirometry according to ATS/ERS guidelines. It will be recorded from three acceptable maneuvers performed in a seated position, and the highest value will be used for analysis.
Baseline and 8 weeks (post-intervention)
Forced expiratory flow at 25-75% of FVC
Délai: Baseline and 8 weeks (post-intervention)
Forced expiratory flow at 25-75% of FVC (FEF25-75) will be assessed using spirometry according to ATS/ERS guidelines. It will be recorded from three acceptable maneuvers performed in a seated position, and the highest value will be used for analysis.
Baseline and 8 weeks (post-intervention)
Maximal inspiratory pressure
Délai: Baseline and 8 weeks (post-intervention)
Maximal inspiratory pressure (MIP) will be assessed using a portable electronic mouth pressure device (MicroRPM; Micro Medical, UK), according to ATS/ERS guidelines. It will be measured in the seated position using a mouthpiece with nasal occlusion. Participants will perform maximal inspiratory effort for at least 2 seconds against an occluded airway. The highest value from three acceptable maneuvers with <10% variability will be recorded in cmH₂O and as a percentage of predicted values using Black and Hyatt reference equations. Higher values indicate better inspiratory muscle strength.
Baseline and 8 weeks (post-intervention)
Maximal expiratory pressure
Délai: Baseline and 8 weeks (post-intervention)
Maximal expiratory pressure (MEP) will be assessed using a portable electronic mouth pressure device (MicroRPM; Micro Medical, UK), according to ATS/ERS guidelines. It will be measured in the seated position using a mouthpiece with nasal occlusion. Participants will perform maximal expiratory effort for at least 2 seconds against an occluded airway. The highest value from three acceptable maneuvers with <10% variability will be recorded in cmH₂O and as a percentage of predicted values using Black and Hyatt reference equations. Higher values indicate better expiratory muscle strength.
Baseline and 8 weeks (post-intervention)
Respiratory muscle endurance
Délai: Baseline and 8 weeks (post-intervention)
Respiratory muscle endurance will be assessed using a constant-load threshold loading test with a pressure threshold device (POWERbreathe Classic Light Resistance, POWERbreathe International Ltd., UK). The test will be performed at 60% of MIP. Participants will breathe through the device for up to 10 minutes, and endurance will be recorded as the time sustained (seconds) and achieved pressure load (cmH₂O). Higher endurance time indicates better respiratory muscle endurance.
Baseline and 8 weeks (post-intervention)
Exercise capacity
Délai: Baseline and 8 weeks (post-intervention)
Exercise capacity will be assessed using the 6-minute walk test (6MWT) according to ATS guidelines. Participants will be instructed to walk as far as possible for 6 minutes along a 30-meter corridor at a self-paced speed. A standardized rest period will be provided prior to testing. Total walking distance will be recorded in meters. Higher walking distance indicates better exercise capacity.
Baseline and 8 weeks (post-intervention)
Dyspnea
Délai: Baseline and 8 weeks (post-intervention)
Dyspnea will be assessed using the Modified Medical Research Council (mMRC) Dyspnea Scale, a 0-4 point scale based on the level of physical activity that induces breathlessness. Higher scores indicate greater severity of dyspnea.
Baseline and 8 weeks (post-intervention)
Fatigue
Délai: Baseline and 8 weeks (post-intervention)
Fatigue will be assessed using the Fatigue Severity Scale (FSS), a 9-item scale evaluating fatigue severity over the past week. Each item is rated on a 7-point Likert scale (1-7), and the total score is calculated by averaging item scores. A score ≥4 indicates severe fatigue. Higher scores indicate greater fatigue severity.
Baseline and 8 weeks (post-intervention)
Fractional exhaled nitric oxide
Délai: Baseline and 8 weeks (post-intervention)
Fractional exhaled nitric oxide (FeNO) will be measured using a NObreath® device (Bedfont Scientific Ltd., UK) according to the ATS guidelines. Measurements will be performed with controlled expiratory flow, and mean values will be recorded. Participants will perform controlled exhalation at a constant flow rate (50 mL/s) following standardized pre-test conditions. The mean of two acceptable measurements will be recorded as FeNO (parts per billion, ppb).
Baseline and 8 weeks (post-intervention)
Frailty
Délai: Baseline and 8 weeks (post-intervention)
Frailty will be assessed using the Edmonton Frail Scale, a 17-point scale evaluating multiple domains including cognition, general health status, functional independence, and social support. Scores range from 0 to 17, with higher scores indicating greater frailty severity.
Baseline and 8 weeks (post-intervention)
Physical performance
Délai: Baseline and 8 weeks (post-intervention)
Physical performance will be assessed using the Short Physical Performance Battery (SPPB), including balance tests, 4-meter gait speed, and chair stand tests. Total scores range from 0 to 12, with higher scores indicating better performance.
Baseline and 8 weeks (post-intervention)
Quality of life (QoL)
Délai: Baseline and 8 weeks (post-intervention)
Quality of life will be assessed using the Minnesota Living with Heart Failure Questionnaire, a 21-item disease-specific scale evaluating the physical and emotional impact of the disease over the past 4 weeks. Each item is scored from 0 to 5, with total scores ranging from 0 to 105. Higher scores indicate worse quality of life.
Baseline and 8 weeks (post-intervention)
Anxiety and depression
Délai: Baseline and 8 weeks (post-intervention)
Anxiety and depression will be evaluated using the Hospital Anxiety and Depression Scale (HADS), a 14-item questionnaire with two subscales assessing anxiety and depression. Each subscale ranges from 0 to 21, with higher scores indicating greater symptom severity.
Baseline and 8 weeks (post-intervention)

Collaborateurs et enquêteurs

C'est ici que vous trouverez les personnes et les organisations impliquées dans cette étude.

Parrainer

Istanbul University - Cerrahpasa

Les enquêteurs

  • Directeur d'études: Rengin Demir, Prof. Dr., Istanbul University - Cerrahpasa

Dates d'enregistrement des études

Ces dates suivent la progression des dossiers d'étude et des soumissions de résultats sommaires à ClinicalTrials.gov. Les dossiers d'étude et les résultats rapportés sont examinés par la Bibliothèque nationale de médecine (NLM) pour s'assurer qu'ils répondent à des normes de contrôle de qualité spécifiques avant d'être publiés sur le site Web public.

Dates principales de l'étude

Début de l'étude (Réel)

27 juillet 2026

Achèvement primaire (Estimé)

1 juillet 2027

Achèvement de l'étude (Estimé)

1 décembre 2027

Dates d'inscription aux études

Première soumission

17 avril 2026

Première soumission répondant aux critères de contrôle qualité

6 mai 2026

Première publication (Réel)

12 mai 2026

Mises à jour des dossiers d'étude

Dernière mise à jour publiée (Réel)

30 juillet 2026

Dernière mise à jour soumise répondant aux critères de contrôle qualité

29 juillet 2026

Dernière vérification

1 juillet 2026

Plus d'information

Termes liés à cette étude

Mots clés

Termes MeSH pertinents supplémentaires

Autres numéros d'identification d'étude

  • 952129

Plan pour les données individuelles des participants (IPD)

Prévoyez-vous de partager les données individuelles des participants (DPI) ?

NON

Informations sur les médicaments et les dispositifs, documents d'étude

Étudie un produit pharmaceutique réglementé par la FDA américaine

Non

Étudie un produit d'appareil réglementé par la FDA américaine

Non

Ces informations ont été extraites directement du site Web clinicaltrials.gov sans aucune modification. Si vous avez des demandes de modification, de suppression ou de mise à jour des détails de votre étude, veuillez contacter register@clinicaltrials.gov. Dès qu'un changement est mis en œuvre sur clinicaltrials.gov, il sera également mis à jour automatiquement sur notre site Web .

S'abonner