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The Effect of Physical Therapy Intervention in Patients With Left Ventricular Assistive Device on Physical Function

The Effect of Physical Therapy Intervention in Patients With Left Ventricular Assistive Device (LVAD) on Physical Function

Status
Completed
Phases
Unknown
Study type
Observational
Source
ClinicalTrials.gov
Registry ID
NCT03636815
Acronym
LVAD
Enrollment
62
Registered
2018-08-17
Start date
2018-04-08
Completion date
2019-03-08
Last updated
2019-09-25

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Left Ventricular Assist Device, Physical Therapy

Keywords

Left ventricular assist device, Physical therapy

Brief summary

To retrospectively investigate the effect of physical therapy intervention on improving physical function of patients post left ventricular assist device (LVAD) through electronic medical record survey

Detailed description

Method: Using portable electronic medical record system in National Taiwan University Hospital (NTUH), retrospectively survey medical record of patients who underwent left ventricular assist device (LVAD) operation in NTUH, compare improvement among those who had received physical therapy intervention and those who hadn't. Inclusion criteria: aged older than 20 years old; diagnosed with heart failure and need LVAD implantation Progress: Note down patients' clinical signs and symptoms, drug usage, imaging findings, physical therapy intervention details, and recovery of functional status. Physical therapy intervention details include: onset symptoms, history, treatment frequency, treatment type, any signs and symptoms during treatment progress and recovery of functional status post physical therapy.

Interventions

OTHERphysical therapy

Cardiopulmonary rehabilitation for patients who receive left ventricle assist device

Sponsors

National Taiwan University Hospital
Lead SponsorOTHER

Study design

Observational model
COHORT
Time perspective
RETROSPECTIVE

Eligibility

Sex/Gender
ALL
Age
20 Years to No maximum
Healthy volunteers
No

Inclusion criteria

* Diagnosed with heart failure, need left ventricular assist device intervention * Over 20 years old * Received physical therapy intervention

Exclusion criteria

* N/A

Design outcomes

Primary

MeasureTime frameDescription
Change in walking functionBaseline, two weeksBy using Six-Minute Walk Test (6MWT), we can obtain the maximum distance that patient can afford walking. In 6 minutes, they should walk as many as they can, on a 15-meter level corridor, assisted device (e.g. cane) can be used if they need. During the test, the patient can stop or rest if they want.

Secondary

MeasureTime frameDescription
Change in Rating Perceived Exertion (RPE)Baseline, two weeksBy using the Borg Rating of Perceived Exertion Scale (score 6-20), the patient subjectively grade the level of perceived exertion after 6MWT.
Change in heart rateBaseline, two weeksWhile doing 6MWT, patients' heart rate will be monitored through portable electrocardiography (ECG) throughout the test. Resting heart rate and heart rate after 6MWT will be recorded.
Change in blood pressureBaseline, two weeksResting blood pressure and blood pressure after 6MWT will be measured.

Countries

Taiwan

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 4, 2026