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Inspiratory Muscle Training and Functional Electrical Stimulation for Treatment of HFpEF (TRAINING-HF)

The safety and scientific validity of this study is the responsibility of the study sponsor and investigators. Listing a study does not mean it has been evaluated by the U.S. Federal Government. Read our disclaimer for details.
 
ClinicalTrials.gov Identifier: NCT02638961
Recruitment Status : Completed
First Posted : December 23, 2015
Last Update Posted : May 18, 2017
Sponsor:
Collaborators:
INCLIVA
Hospital Clínico Universitario de Valencia
Information provided by (Responsible Party):
Universitat Jaume I

Brief Summary:
Heart failure (HF) with preserved ejection fraction (HFpEF) has become the most prevalent form of HF in developed countries. Despite its increasing in prevalence, there is no evidence-based effective therapy for HFpEF The purpose of this study was to evaluate whether inspiratory muscle training (IMT), functional electrical stimulation (FES), or combination of both improve exercise capacity as well as left ventricular diastolic function, biomarkers' profile, quality of life (QoL) and prognosis in patients with HFpEF.

Condition or disease Intervention/treatment Phase
Heart Failure With Normal Ejection Fraction Other: IMT Other: FES Other: Standard treatment Not Applicable

Detailed Description:

This study was designed as a prospective, controlled, randomized, four-armed, efficacy trial of patients with the diagnosis of HFpEF and New York Heart Association functional class II-III/IV, diagnosed according to criteria of the European Society of Cardiology. A computer-generated randomization scheme was used to allocate participants (in a 1:1:1:1 ratio) to receive: 1) a home-based 12-week program of inspiratory muscle training (IMT) or; 2) a 12-week program of functional electrical stimulation (FES) of lower limb muscles or; 3) standard treatment (ST) alone or; 4) combination of IMT and FES. The study is being conducted in a single center in Spain. Independently of staggered entry, the minimum duration of a patient's participation is 6 months (from first to last visit). All patients will provide signed informed consent and the protocol has been approved by the research ethics committee of our center in accordance with the principles of the Declaration of Helsinki and national regulations.

Study population Candidate patients are selected from the outpatient's clinics of HF of the Hospital Clínico Universitario of Valencia.

Study objectives The primary endpoint of the study is a clinical endpoint of three and six months change in peak oxygen uptake (peak VO2).

Secondary endpoints are three and six month changes in echocardiogram parameters, QoL and prognostic biomarkers. The investigators also will specifically focus on number of episodes of worsening HF at 6 months:

  1. Change in E/e' after three and six months.
  2. Change in left atrial volume index after three and six months.
  3. Change in health-related QoL measured by the Minnesota Living With Heart Failure Questionnaire (MLHF) after three and six months.
  4. Change in natriuretic peptide (NT-proBNP) after three and six months.
  5. Change in minute ventilation/carbon dioxide production (VE/VCO2) slope after three and six months.
  6. Number of episodes of acute HF hospitalizations and number of episodes of worsening HF not requiring hospitalization at 6 months.

Intervention

Eligibility assessment and screening visit After reviewing the inclusion/exclusion criteria and signing the informed consent form, a comprehensive medical history, physical examination, anthropometry and examination tests will be performed. The examination tests include: electrocardiogram (ECG) echocardiography, cardiopulmonary exercise testing (CPET), 6-minute walk test (6-MWT), inspiratory muscle function test, QoL assessment by the Minnesota Living With Heart Failure Questionnaire (MLHF) and blood samples for a panel of baseline biomarkers.

Finally, patients are randomized (1:1:1:1) to four groups: 1) ST alone or; 2) a home-based 12-week program of IMT or; 3) a 12-week program of FES or; 4) combination of IMT and FES (IMT+FES) during 12 weeks.

12-week and six months visits All patients will be evaluated after 12-week supervised training, and six months after randomization. Evaluation will include medical history, physical examination, anthropometry and functional and QoL assessment tests (ECG, CPET, 6-MWT, inspiratory muscle function test, MLHF and blood tests).

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Study Type : Interventional  (Clinical Trial)
Actual Enrollment : 52 participants
Allocation: Randomized
Intervention Model: Parallel Assignment
Masking: None (Open Label)
Primary Purpose: Treatment
Official Title: Inspiratory Muscle Training and Functional Electrical Stimulation for Treatment of Heart Failure With Preserved Ejection Fraction
Study Start Date : October 2015
Actual Primary Completion Date : January 2017
Actual Study Completion Date : March 2017

Resource links provided by the National Library of Medicine

MedlinePlus related topics: Heart Failure

Arm Intervention/treatment
Placebo Comparator: Standard treatment
Only standard medical treatment
Other: Standard treatment
Patients allocated to this arm will not receive any physical therapy, only standard medical treatment. They will be checked weekly by a physiotherapist who measures their maximal inspiratory mouth pressure each time.

Active Comparator: IMT group
Standard medical treatment associated to Inspiratory muscle training
Other: IMT
Patients allocated to IMT arm will receive standard medical treatment and will be instructed to train at home twice daily, for 20 minutes each session, and during 12 weeks using a threshold inspiratory muscle trainer (Threshold IMT®, Respironics Inc.). All of them will be instructed by a respiratory therapist and educated to maintain a diaphragmatic breathing during the training period. The subjects start breathing at a resistance equal to 25-30% of their maximal inspiratory pressure (MIP) for 1 week. The respiratory therapist examines the patients at weekly intervals by checking the diary card and measuring their MIP each time. The resistance is modified each session according to their 25-30% of their MIP measured.
Other Name: Inspiratory muscular training

Active Comparator: FES group
Standard medical treatment associated to functional electrostimulation of both legs for 45 minutes a day, 2 days per week for a total of 12 weeks.
Other: FES
Patients allocated to FES arm will receive standard medical treatment and will be trained in a FES program of both legs by a physiotherapist for 45 minutes a day, 2 days per week for a total of 12 weeks. Eight adhesive electrodes are positioned on the skin over the quadriceps and gastrocnemius muscles of both legs. The stimulator is configured to deliver a direct electrical current at 25 Hz for 5 seconds followed by a 5-second rest. The intensity of the stimulation is adjusted to achieve a visible muscle contraction without discomfort.
Other Name: Functional electrostimulation of lower limbs

Active Comparator: IMT+FES group
Standard medical treatment associated to combination of inspiratory muscle training and functional electrostimulation of both legs
Other: IMT
Patients allocated to IMT arm will receive standard medical treatment and will be instructed to train at home twice daily, for 20 minutes each session, and during 12 weeks using a threshold inspiratory muscle trainer (Threshold IMT®, Respironics Inc.). All of them will be instructed by a respiratory therapist and educated to maintain a diaphragmatic breathing during the training period. The subjects start breathing at a resistance equal to 25-30% of their maximal inspiratory pressure (MIP) for 1 week. The respiratory therapist examines the patients at weekly intervals by checking the diary card and measuring their MIP each time. The resistance is modified each session according to their 25-30% of their MIP measured.
Other Name: Inspiratory muscular training

Other: FES
Patients allocated to FES arm will receive standard medical treatment and will be trained in a FES program of both legs by a physiotherapist for 45 minutes a day, 2 days per week for a total of 12 weeks. Eight adhesive electrodes are positioned on the skin over the quadriceps and gastrocnemius muscles of both legs. The stimulator is configured to deliver a direct electrical current at 25 Hz for 5 seconds followed by a 5-second rest. The intensity of the stimulation is adjusted to achieve a visible muscle contraction without discomfort.
Other Name: Functional electrostimulation of lower limbs




Primary Outcome Measures :
  1. Functional capacity measured as peak oxygen uptake (peak VO2) in ml/min/kg . [ Time Frame: changes at 12 weeks and 6 months ]

    Maximal functional capacity will be evaluated with an incremental and symptom-limited cardiopulmonary exercise testing (CORTEX Metamax 3B) on a bicycle ergometer, beginning with a workload of 10 W and increasing stepwise at 10-W increments every 1 min. During exercise, patients were continuously monitored with twelve-lead electrocardiogram and blood pressure measurements every 2 min. Gas exchange data and cardiopulmonary variables were averaged every 10 seconds values. Peak VO2 is considered the highest value of VO2 during the last 20 s of exercise.

    The improvement > of 10% in peak VO2 will be considered clinically meaningful



Secondary Outcome Measures :
  1. Functional capacity measured as distance walked in 6 minutes [ Time Frame: changes at 12 weeks and 6 months ]
    Patients will be instructed to cover the maximum distance (meters) possible in six minutes, at a self-graded walking speed, pausing to rest when needed. Each subject will undergo 4 tests. The goal of the first one was to allow the patient to familiarize with the test.

  2. Change in echocardiographic parameter of diastolic disfunction: e' septal (cm/s) [ Time Frame: changes in rest at 12 weeks and 6 months ]

    Doppler echocardiogram examination of e' septal (cm/s) will be performed under resting conditions using 2D echocardiography (iE33, Philips). e' septal (cm/s) parameter will be measured according to current guidelines of the European Society of Echocardiography:

    Only significant improvements in this parameter will be considered


  3. Change in echocardiographic parameter of diastolic disfunction: left atrial volume index (mm/m2) [ Time Frame: changes in rest at 12 weeks and 6 months ]

    Doppler echocardiogram examination of left atrial volume index (mm/m2) will be performed under resting conditions using 2D echocardiography (iE33, Philips). Left atrial volume index (mm/m2) will be measured according to current guidelines of the European Society of Echocardiography.

    Only significant improvements in this parameter will be considered


  4. Change in echocardiographic parameter of diastolic disfunction: E/e' ratio [ Time Frame: changes in rest at 12 weeks and 6 months ]

    Doppler echocardiogram examination of E/e' ratio will be performed under resting conditions using 2D echocardiography (iE33, Philips). E/e' ratio parameter will be measured according to current guidelines of the European Society of Echocardiography.

    Only significant improvement in this parameter will be considered


  5. Change in health-related QoL [ Time Frame: changes at 12 weeks and 6 months ]
    Change in health-related QoL will be measured by the Minnesota Living With Heart Failure Questionnaire (no units) Only significant improvements in these parameters will be considered

  6. Number of rehospitalizations or worsening HF at 6 months [ Time Frame: changes at 6 months ]
    Number of episodes of acute HF hospitalizations and number of episodes of worsening HF not requiring hospitalization at 6 months among different arms.



Information from the National Library of Medicine

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Ages Eligible for Study:   18 Years and older   (Adult, Older Adult)
Sexes Eligible for Study:   All
Accepts Healthy Volunteers:   No
Criteria

Inclusion Criteria:

  • Previous history of symptomatic heart failure NYHA (New York Heart Association )functional class ≥II with Normal left ventricular ejection fraction:

    • ejection fraction >0.50 by Simpson method
    • end-diastolic diameter <60 mm
  • Structural heart disease:

    • left ventricle hypertrophy/left atrial enlargement and/or
    • diastolic dysfunction estimated by 2D echocardiography
  • Previous admission for acute heart failure
  • Clinical stability, without hospital admissions in the past 3 month

Exclusion Criteria:

  • Perform a valid baseline exercise test
  • Significant primary moderate to severe valvular disease
  • Acute coronary syndrome or cardiac surgery within the previous three months
  • Signs of ischemia during cardiopulmonary exercise testing
  • Significant primary pulmonary disease; including pulmonary arterial hypertension, chronic thromboembolic pulmonary disease or chronic obstructive pulmonary disease
  • Any other comorbidity with an expectancy of life less than one year

Information from the National Library of Medicine

To learn more about this study, you or your doctor may contact the study research staff using the contact information provided by the sponsor.

Please refer to this study by its ClinicalTrials.gov identifier (NCT number): NCT02638961


Locations
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Spain
Hospital clínico universitario de Valencia
Valencia, Spain, 46010
Sponsors and Collaborators
Universitat Jaume I
INCLIVA
Hospital Clínico Universitario de Valencia
Investigators
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Principal Investigator: Patricia Palau, M.D., PhD Universitat Jaume I
Study Director: Eloy Domínguez, M.D Universitat Jaume I
Study Chair: Julio Núñez, M.D., PhD Universitat de Valencia
Publications:
Publications automatically indexed to this study by ClinicalTrials.gov Identifier (NCT Number):
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Responsible Party: Universitat Jaume I
ClinicalTrials.gov Identifier: NCT02638961    
Other Study ID Numbers: IMT-FES 01
First Posted: December 23, 2015    Key Record Dates
Last Update Posted: May 18, 2017
Last Verified: May 2017
Keywords provided by Universitat Jaume I:
heart failure with preserved ejection fraction
physical therapy
exercise capacity
quality of life
Additional relevant MeSH terms:
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Heart Failure
Heart Diseases
Cardiovascular Diseases