Actively Recruiting

Phase Not Applicable
Age: 18Years - 70Years
All Genders
NCT06426173

Effect of Resistance Training in Patients on the Waiting List for Heart Transplant

Led by University of Sao Paulo General Hospital · Updated on 2024-06-21

50

Participants Needed

1

Research Sites

127 weeks

Total Duration

On this page

Sponsors

U

University of Sao Paulo General Hospital

Lead Sponsor

C

Conselho Nacional de Desenvolvimento Científico e Tecnológico

Collaborating Sponsor

AI-Summary

What this Trial Is About

The present longitudinal, randomized, and blinded clinical trial aims to: * Evaluate the effects of resistance training on the functional capacity, quality of life, and cardiac biomarkers of hospitalized patients with heart failure (HF) on the waiting list for heart transplantation (HTx). * Evaluate the associations between Fried's frailty classification and functional capacity responses to resistance training. The protocol will have a total duration of 12 weeks.

CONDITIONS

Official Title

Effect of Resistance Training in Patients on the Waiting List for Heart Transplant

Who Can Participate

Age: 18Years - 70Years
All Genders

Eligibility Criteria

Eligible

You may qualify if you...

  • Patients included in the heart transplant list for less than or equal to 1 month
  • Hemodynamically stable in the last 48 hours defined as mean arterial pressure (MAP) between 60 and 120 mmHg and heart rate (HR) between 60 bpm and 120 bpm
  • Dobutamine dose less than or equal to 10 mcg/kg/min
Not Eligible

You will not qualify if you...

  • Heart failure of arrhythmogenic and/or restrictive etiology
  • Presence of uncontrolled acute arrhythmias
  • Cognitive, orthopedic, or neuromotor changes that prevent functional tests from being carried out

AI-Screening

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Trial Site Locations

Total: 1 location

1

Instituto do Coração - Hospital das Clínicas da Faculdade de Medicina da Universidade de São Paulo

São Paulo, Brazil, 05403-000

Actively Recruiting

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Research Team

J

Juliana A Nascimento, PT, PhD

CONTACT

R

Rafael M Ianotti, PT

CONTACT

How is the study designed?

Study Type

INTERVENTIONAL

Masking

SINGLE

Allocation

RANDOMIZED

Model

PARALLEL

Primary Purpose

TREATMENT

Number of Arms

2

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