NCT03084679

Brief Summary

The investigators hypothesised that novel MRI metrics derived from myocardium post-gadolinium T1 mapping analysis will improve the current knowledge about the role interstitial fibrosis and cardiomyocyte hypertrophy in the development of left ventricular (LV) remodelling and clinical Heart Failure (HF). The investigators believe that these recently described variables will be associated with prognostically important indices in HF development.

Trial Health

43
At Risk

Trial Health Score

Automated assessment based on enrollment pace, timeline, and geographic reach

Trial has exceeded expected completion date
Enrollment
90

participants targeted

Target at P50-P75 for not_applicable heart-failure

Timeline
Completed

Started Nov 2017

Typical duration for not_applicable heart-failure

Geographic Reach
1 country

1 active site

Status
unknown

Health score is calculated from publicly available data and should be used for screening purposes only.

Trial Relationships

Click on a node to explore related trials.

Study Timeline

Key milestones and dates

First Submitted

Initial submission to the registry

December 25, 2016

Completed
3 months until next milestone

First Posted

Study publicly available on registry

March 21, 2017

Completed
8 months until next milestone

Study Start

First participant enrolled

November 1, 2017

Completed
1.6 years until next milestone

Primary Completion

Last participant's last visit for primary outcome

June 1, 2019

Completed
1.1 years until next milestone

Study Completion

Last participant's last visit for all outcomes

July 1, 2020

Completed
Last Updated

June 5, 2019

Status Verified

June 1, 2019

Enrollment Period

1.6 years

First QC Date

December 25, 2016

Last Update Submit

June 3, 2019

Conditions

Keywords

Heart FailureHypertrophyFibrosisMagnetic Resonance

Outcome Measures

Primary Outcomes (1)

  • Myocardial remodeling assessed by CMR in rehabilitation vs usual care.

    Investigate whether rehabilitation compared to usual care is associated with significant favorable myocardial remodeling assessed by CMR determination of ECV.

    4 months

Secondary Outcomes (17)

  • Change in left ventricular ejection fraction

    4 months

  • Change in right ventricular ejection fraction

    4 months

  • Change in left ventricular mass (absolute/index)

    4 months

  • Change in left ventricular diastolic volume (absolute/index)

    4 months

  • Change in right ventricular diastolic volume (absolute/index)

    4 months

  • +12 more secondary outcomes

Study Arms (4)

Conventional Clinical Care - HFpEF

NO INTERVENTION

Heart Failure patients with preserved ejection fraction (HFpEF) randomized to this arm will keep receiving their conventional clinical care, being instructed to continue and maintain their usual daily activities.

Supervised Exercise Training- HFpEF

OTHER

Heart Failure patients with preserved ejection fraction (HFpEF) randomized to this arm will keep receiving their conventional clinical care and participate in a supervised, facility based training program consisting of stretching exercises and aerobic exercise in treadmill.

Other: Aerobic exercise in treadmillOther: Local strengthening exercisesOther: Stretching exercises

Conventional Clinical Care - HFrEF

NO INTERVENTION

Heart Failure patients with reduced ejection fraction (HFrEF) randomized to this arm will keep receiving their conventional clinical care, being instructed to continue and maintain their usual daily activities.

Supervised Exercise Training - HFrEF

OTHER

Heart Failure patients with reduced ejection fraction (HFrEF) randomized to this arm will keep receiving their conventional clinical care and participate in a supervised, facility based training program consisting of stretching exercises and aerobic exercise in treadmill.

Other: Aerobic exercise in treadmillOther: Local strengthening exercisesOther: Stretching exercises

Interventions

30-40min of aerobic exercise in treadmill. The aerobic intensity will be established by heart rate levels that corresponded to anaerobic threshold up to 10% below the respiratory compensation point obtained in the cardiopulmonary exercise test. This intensity corresponded to 60-72% peak V̀‡o2. During the exercise sessions, when a training effect will be observed, as indicated by a decrease by 8 to 10% in heart rate, the treadmill velocity or inclination will be increased to return to the target heart rate levels.

Supervised Exercise Training - HFrEFSupervised Exercise Training- HFpEF

15 min of local strengthening exercises will be performed in major muscle groups (legs, arms and trunk muscles): three series of each exercise, 12-15 repetitions.

Supervised Exercise Training - HFrEFSupervised Exercise Training- HFpEF

5-min stretching exercises will be performed in major muscle groups (legs, arms and trunk muscles)

Supervised Exercise Training - HFrEFSupervised Exercise Training- HFpEF

Eligibility Criteria

Age18 Years+
Sexall
Healthy VolunteersNo
Age GroupsAdult (18-64), Older Adult (65+)

You may qualify if:

  • Age\> 18 years
  • Functional limitation (New York Heart Association Class II or worse)
  • No contraindication to exercise (American College of Cardiology / American Heart Association criteria)
  • Eligibility to take MRI (absence of metallic devices, and glomerular filtration rate \> 40ml / min / 1.73m2, etc.)
  • Prior diagnosis of Heart Failure (by the Framingham criterion)
  • Therapy with diuretic and euvolemia state (evaluated by cardiologist and cardiopulmonary exercise testing)
  • Transthoracic echocardiogram

You may not qualify if:

  • Severe ischemia in any stress test
  • Hypertrophic cardiomyopathy or any infiltrative heart disease
  • Chronic obstructive pulmonary disease , pulmonary hypertension (Pulmonary artery pressure\> 60mmHg)
  • Severe left or right valve disease.
  • Pacemaker or implantable cardioverter defibrillator
  • Myocardial infarction or revascularization in 3 months
  • Anemia (hemoglobin \<10 grams / dl) until 1 month before cardiopulmonary exercise testing

Contact the study team to confirm eligibility.

Sponsors & Collaborators

Study Sites (1)

University of Campinas

Campinas, SĂ£o Paulo, Brazil

RECRUITING

Related Publications (44)

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    PMID: 14734125BACKGROUND
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    PMID: 11395543BACKGROUND
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    PMID: 9223325BACKGROUND
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    PMID: 9568714BACKGROUND
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    PMID: 11705790BACKGROUND
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    PMID: 15623566BACKGROUND
  • Strom CC, Aplin M, Ploug T, Christoffersen TE, Langfort J, Viese M, Galbo H, Haunso S, Sheikh SP. Expression profiling reveals differences in metabolic gene expression between exercise-induced cardiac effects and maladaptive cardiac hypertrophy. FEBS J. 2005 Jun;272(11):2684-95. doi: 10.1111/j.1742-4658.2005.04684.x.

    PMID: 15943803BACKGROUND
  • Mujumdar VS, Tyagi SC. Temporal regulation of extracellular matrix components in transition from compensatory hypertrophy to decompensatory heart failure. J Hypertens. 1999 Feb;17(2):261-70. doi: 10.1097/00004872-199917020-00011.

    PMID: 10067796BACKGROUND
  • Querejeta R, Lopez B, Gonzalez A, Sanchez E, Larman M, Martinez Ubago JL, Diez J. Increased collagen type I synthesis in patients with heart failure of hypertensive origin: relation to myocardial fibrosis. Circulation. 2004 Sep 7;110(10):1263-8. doi: 10.1161/01.CIR.0000140973.60992.9A. Epub 2004 Aug 16.

    PMID: 15313958BACKGROUND
  • van Heerebeek L, Borbely A, Niessen HW, Bronzwaer JG, van der Velden J, Stienen GJ, Linke WA, Laarman GJ, Paulus WJ. Myocardial structure and function differ in systolic and diastolic heart failure. Circulation. 2006 Apr 25;113(16):1966-73. doi: 10.1161/CIRCULATIONAHA.105.587519. Epub 2006 Apr 17.

    PMID: 16618817BACKGROUND
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    PMID: 23963758BACKGROUND
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    PMID: 23725816BACKGROUND
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    PMID: 22991405BACKGROUND
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    PMID: 23443441BACKGROUND
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    PMID: 24716680BACKGROUND
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MeSH Terms

Conditions

Heart FailureHypertrophyFibrosis

Interventions

ExerciseMuscle Stretching Exercises

Condition Hierarchy (Ancestors)

Heart DiseasesCardiovascular DiseasesPathological Conditions, AnatomicalPathological Conditions, Signs and SymptomsPathologic Processes

Intervention Hierarchy (Ancestors)

Motor ActivityMovementMusculoskeletal Physiological PhenomenaMusculoskeletal and Neural Physiological PhenomenaExercise TherapyRehabilitationAftercareContinuity of Patient CarePatient CareTherapeuticsPhysical Therapy Modalities

Study Officials

  • OTAVIO R COELHO-FILHO, MD, MPH, PhD

    University of Campinas, Brazil

    PRINCIPAL INVESTIGATOR

Central Study Contacts

OTAVIO R COELHO-FILHO, MD, MPH, PhD

CONTACT

FERNANDO B CARDOSO, MD

CONTACT

Study Design

Study Type
interventional
Phase
not applicable
Allocation
RANDOMIZED
Masking
NONE
Purpose
TREATMENT
Intervention Model
PARALLEL
Model Details: Randomized trial in a 2:1 (intervention:control) proportion and in blocks of 6 participants.
Sponsor Type
OTHER
Responsible Party
PRINCIPAL INVESTIGATOR
PI Title
Assistant Professor

Study Record Dates

First Submitted

December 25, 2016

First Posted

March 21, 2017

Study Start

November 1, 2017

Primary Completion

June 1, 2019

Study Completion

July 1, 2020

Last Updated

June 5, 2019

Record last verified: 2019-06

Data Sharing

IPD Sharing
Will not share

No plan to Share individual participant data.

Locations