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Active, not recruitingNCT07045649Updated Jul 14, 2026

Association Between the Sit-To-Stand Test and the Prognosis of Patients With Heart Failure

An observational study in Heart Failure, Heart Failure NYHA Class IV and Heart Failure; With Decompensation, sponsored by Centro Universitário Augusto Motta. Active, not recruiting at 1 site in Brazil. Open to participants aged 18 Years and older. Per ClinicalTrials.gov, last updated 2026-07-14.

Sponsored by Centro Universitário Augusto Motta · Observational

From the registry’s dates

  • Primary completion was expected by Jul 2026, 3 months ago, but the record still lists the study as active, not recruiting.
Study type
Observational
Model
Cohort
Time perspective
Prospective
Enrollment
68
Ages
18 Years and older
Sex
All
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Study summary

Introduction: Heart failure (HF), among cardiovascular diseases, is the disease that has been increasing its incidence and prevalence the most in recent years in the world population, due to the aging of the population. In addition, HF is the most frequent hospital diagnosis in the elderly, and is the main cause of hospitalization, with significant expenditure in public and private health care worldwide. Some functional tests have been used to predict the prognosis in patients with HF, however, the use of the 1-minute sit-to-stand test (SST1) to predict prognosis in HF has little scientific evidence, due to the lack of studies found in the literature for this population. Thus, the present study aims to evaluate the association between SST1 at discharge from the Cardio Intensive Care Unit (ICU) and the clinical outcome after 90 days in patients hospitalized for decompensated heart failure (DHF). Methods: This is a prospective cohort study analyzing the association between performance on the TSL1 and clinical outcome in patients hospitalized for DHF from June 2025 to October 2025. Sociodemographic, family, social, and clinical data will be collected from the participants, after which the TSL1 will be performed. The outcome of death and hospital readmission within 90 days after discharge from the ICU will be identified through telephone contact, which will be carried out by the researcher. Expected results: It is expected that from the results of this study it will be possible to understand whether performance on the TSL1 predicts clinical outcome for patients hospitalized for DHF and that it will even be possible to determine a cutoff point capable of predicting the outcomes of interest.

Read the detailed description

This is a prospective cohort study analyzing the association between TSL1 performance and clinical and functional outcomes within 90 days after discharge of patients who were hospitalized for CDI between June 2025 and October 2025. Data will be collected by the researcher and the institution's senior physiotherapist team, and the team will be trained to reduce the risk of bias. A document form will be made available for completion during the evaluation, and sociodemographic data will also be collected from the electronic medical record.

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Conditions studied

  • Heart Failure
  • Heart Failure NYHA Class IV
  • Heart Failure; With Decompensation
  • Heart Failure NYHA Class III
  • Heart Failure NYHA Class II

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Keywords

  • Functional Status
  • Hospitalization
  • Prognosis
03

In context

Heart Failure

5,701 studies on the registry are indexed under Heart Failure; 1,220 are open to participants now.

This study's planned enrollment of 68 is below the median of 200 across 1,679 observational studies indexed under Heart Failure.

Browse Heart Failure studies →

Lead sponsor

Centro Universitário Augusto Motta is the lead sponsor of 39 studies on the registry; 14 are open to participants now.

Counted across the registry records on this site, refreshed daily.

04

Who can participate

Ages eligible
18 Years and older
Sexes eligible
All
Accepts healthy volunteers
No
Sampling method
Non-probability sample

Study population

Patients diagnosed with CDI

Inclusion criteria

  • Patients diagnosed with CDI;
  • Over 18 years of age;
  • With an Intensive Care Unit Mobility Scale (IMS) > 4 at discharge from the ICU;
  • Able to sit and stand up from a chair without support from the upper limbs (ULs) will be included in the study.

Exclusion criteria

Exclusion Criteria:

  • Patients with cognitive alterations;
  • Level of consciousness, with [RASS (Richmond Agitation and Sedation Scale) >+1 or \<-2 and Glasgow \<13 (Coma Scale)], neurological and orthopedic, which compromise the understanding and performance of the assessment will be excluded;
  • Patients with advanced invasive ventilatory and circulatory support or in cardiogenic shock.
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Study design

Observational model
Cohort
Time perspective
Prospective
Enrollment
68 participants (estimated)
Patient registry
No

Groups and cohorts

  • 1-minute sit-to-stand test

    The 1-minute sit-to-stand test will be assessed upon discharge from the Cardiac Intensive Care Unit. It may be assessed up to 48 hours after discharge from the unit. It will be performed on a standardized 46.0 cm chair without armrests, placed against the wall. Participants will be seated in the chair, without support, with their knees and hips at 90° flexion, with their feet parallel to the floor and their arms crossed over their chest. Participants will be instructed to stand up and sit down as quickly as possible without using their arms for 1 minute and will be instructed to stop whenever they wish. However, they must return as quickly as possible, since the goal is to complete as many repetitions as possible in 1 minute. Vital signs and dyspnea and leg fatigue will be assessed using the Modified Borg Scale before and after the test. A repetition will be identified as standing up completely straight and returning to the sitting position.

    Diagnostic Test: 1-minute sit-to-stand test

Interventions

  • Diagnostic test1-minute sit-to-stand test

    The 1-minute sit-to-stand test will be assessed upon discharge from the Cardiac Intensive Care Unit. It may be assessed up to 48 hours after discharge from the unit. It will be performed on a standardized 46.0 cm chair without armrests, placed against the wall. Participants will be seated in the chair, without support, with their knees and hips at 90° flexion, with their feet parallel to the floor and their arms crossed over their chest. Participants will be instructed to stand up and sit down as quickly as possible without using their arms for 1 minute and will be instructed to stop whenever they wish. However, they must return as quickly as possible, since the goal is to complete as many repetitions as possible in 1 minute. Vital signs and dyspnea and leg fatigue will be assessed using the Modified Borg Scale before and after the test. A repetition will be identified as standing up completely straight and returning to the sitting position.

06

What researchers measure

Primary outcomes

  1. Occurrence of mortality for any cause within 90 days after discharge from the Cardiac Intensive Care Unit (ICU) in patients hospitalized for decompensated heart failure (DHF).

    Time frame: 90 days after discharge from the ICU

  2. Number of readmission for any cause within 90 days after discharge from the Cardiac Intensive Care Unit (ICU) in patients hospitalized for decompensated heart failure (DHF).

    Time frame: 90 days after discharge from the ICU

Secondary outcomes

  1. All-cause mortality within 90 days of discharge

    Time frame: 90 days after discharge from the ICU

  2. Readmission due to HF within 90 days after discharge

    Time frame: 90 days after discharge from the ICU

  3. Total number of days alive outside the hospital (days alive after discharge by time from occurrence to event) in the first 90 days after discharge

    Time frame: 90 days after discharge from the ICU

  4. Functional performance at the time of discharge from the ICU according to the IMS - Intensive Care Unit Mobility Scale

    Time frame: In the 48 hours prior to discharge from the ICU

  5. Correlation between TSL-1 performance and other functional markers at discharge (FSS-ICU, IMS and handgrip strength)

    Time frame: In the 48 hours prior to discharge from the ICU

07

Study locations

1 site
  • Hospital Universitário Pedro Ernesto
    Rio de Janeiro, Rio de Janeiro 20551-030, Brazil
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References and documents

Individual participant data

Plan to share: No

No publications or documents are linked to this record.

09

Updates

Tracking since Sep 25, 2026
No changes since tracking began. The registry record was last updated on Jul 14, 2026, before this site started recording changes on Sep 25, 2026. Its history is on ClinicalTrials.gov ↗
10

Registry details

Key details

Study ID
NCT07045649
Lead sponsor
Centro Universitário Augusto Motta
Responsible party
Sponsor
First posted
Jul 1, 2025
Start date
Jul 16, 2025
Primary completion
Jul 2026 (estimated)
Completion
Aug 2026 (estimated)
Last update
Jul 14, 2026

Oversight

Data monitoring committee
Yes
FDA-regulated drug
No
FDA-regulated device
No
View the source record on ClinicalTrials.gov ↗

Not currently enrolling

This study is active, not recruiting, as verified in Jul 2025. You cannot join it, but the record below documents what was studied.

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