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The Use of Samsung Health and ECG M-Trace Base II Applications in the Secondary Prevention After Stroke

P

Poznan University of Medical Sciences (PUMS)

Status

Completed

Conditions

Stroke
Secondary Prevention
Mobile Applications

Study type

Observational

Funder types

Other

Identifiers

Details and patient eligibility

About

The aim of the present study was to quantitatively assess the risk factors that may affect the re-occurrence of a CVD event and the use of a commercially available mobile application Samsung Health for the assessment of parameters of exercise tolerance and the ECG M-Trace Base II application for the assessment of cardiological parameters.

Full description

In the post-stroke group and in the control group, SMWT (Six Minute Walk Test) and SCT( Stair Climb Test) were preceded by a 10-minute rest in sitting position. The time of test performance, the walked distance and steps made as well as the mean and maximum gait velocity and the calories burned were assessed using the above-mentioned Samsung Health application . ECG results were assessed with the use of ECG M-Trace Base II application described above. In addition, cardiological parameters such as: systolic blood pressure (SBP) and diastolic blood pressure (DBP), heart rate (HR) and arterial blood saturation were assessed. The measurements were performed at rest and directly after SCMT and SCT. Additionally, after the tests, the level of dyspnoea and fatigue was assessed according to the modified Borg scale (score 0-10).

Enrollment

52 patients

Sex

All

Ages

42 to 65 years old

Volunteers

Accepts Healthy Volunteers

Inclusion and exclusion criteria

Inclusion criteria to the post-stroke group were as follows :

  1. occurrence of hemiparesis after the first episode of ischaemic stroke
  2. stroke confirmed in the diagnostic imaging records
  3. score >3 on Lovett's scale of muscle strength in the paretic limbs
  4. score above 15 in Barthel's scale of performance in activities of daily living
  5. score below 12 in the National Institutes of Health Stroke Scale (NIHSS)
  6. available complete medical records concerning the assessed risk factors of recurrent CVD event
  7. lack of concomitant pulmonary diseases including chronic obstructive pulmonary disease and bronchial asthma

Exclusion criteria from the post-stroke group were as follows:

  1. hemiparesis or tetraparesis following many episodes of stroke,
  2. lack of diagnostic imaging scans confirming the occurrence of stroke
  3. hospital stay at the Department of Neurological Rehabilitation for more than 14 days from the occurrence of stroke
  4. incomplete medical records concerning the assessed risk factors of recurrent CVD event
  5. score >3 on Lovett's scale of muscle strength in the paretic limbs
  6. score below 14 in Barthel's scale of performance in activities of daily living
  7. score above 13 in the NIHSS scale
  8. occurrence of factors limiting walking ability, such as diagnosed pulmonary diseases, unstable angina, severe valvular heart diseases, cardiomyopathy, musculoskeletal or autoimmune diseases.

Trial design

52 participants in 2 patient groups

The study group (post-stroke)
Description:
The study group consisted of 26 patients in whom ischaemic brain stroke occurred within 14 days before the admission to the Clinical Department, and were hospitalised at the Department of Neurological Rehabilitation of the Clinical Department of Rehabilitation in the Wiktor Dega Orthopaedic and Rehabilitation Clinical Hospital in Poznań
The control group
Description:
The control group was composed of 26 healthy individuals recruited from the hospital staff who did not experience stroke.

Trial contacts and locations

1

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Data sourced from clinicaltrials.gov

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