Heart Rate Variability in Duchenne Muscular Dystrophy During Computer Task
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|ClinicalTrials.gov Identifier: NCT04607824|
Recruitment Status : Completed
First Posted : October 29, 2020
Last Update Posted : October 29, 2020
|Condition or disease||Intervention/treatment|
|Duchenne Muscular Dystrophy||Behavioral: Duchenne Muscular Dystrophy group Behavioral: Typical Development group|
This is a cross-sectional study, where HR was recorded beat-to-beat (RR intervals) using the portable Polar RS800CX HR monitor (Polar Electro, Finland). HR was recorded before the onset and at the end of the five minutes of the computer maze paradigm task.
The subjects were seated in a standard chair (walkers, TD group and DMD) or in their own wheelchair (non-walkers, DMD group), the Polar watch was positioned on the wrist. The analysis of HRV was possible through the recording of RR interval in two periods: the period of twenty minutes at seated rest, and then during the computer task for five minutes.
The computer task used a maze paradigm with one correct pathway that could be negotiated and ultimately solved. All participants were positioned comfortably and an evaluator responsible for instruction and annotation of data.
Each individual was instructed to walk the correct path with the digital character pawn (pointed on the screen by the evaluator) to the exit of the maze identified by an "x" (pointed on the screen by the evaluator). It was provided for the subjects, who used the arrow buttons on the keyboard, identified by up, down, right and left, using the dominant hand, with the arrows moving through a 20 x 20 cm maze. Participants were requested to complete the maze as fast as possible.
HRV analysis followed the guidelines published by the Task Force of the European Society of Cardiology and North American Society of Pacing and Electrophysiology. The RR intervals were recorded, and then were downloaded to the Polar Precision Performance program (v.3.0). This software enabled the visualization of HR and the extraction of a cardiac period (RR intervals series; the variation of beat-to-beat interval in milliseconds) file in ".txt" format. For analysis of HRV data at rest, we analyzed 1000 consecutive RR intervals, and for HRV analysis for the computational task, the number of consecutive RR intervals obtained was exactly 256 RR intervals. Digital filtering complemented by manual filtering was performed to eliminate artifacts and only series with greater than 95% of sinus beats were included in the study. HRV analysis was undertaken through linear, non-linear and chaotic global techniques (CGT).
|Study Type :||Observational|
|Actual Enrollment :||90 participants|
|Official Title:||Computational Task in Duchenne Muscular Dystrophy: Involvement of Cardiac Autonomic Regulation.|
|Actual Study Start Date :||March 2014|
|Actual Primary Completion Date :||December 2014|
|Actual Study Completion Date :||June 2020|
Duchenne Muscular Dystrophy group
Forty-five male subjects were included in the Duchenne Muscular Dystrophy (DMD) group and they were assessed for twenty minutes at rest sitting, and then five minutes whilst performing the maze task on a computer.
Behavioral: Duchenne Muscular Dystrophy group
Assessment of heart rate variability at rest and during computational task in people with Duchenne muscular dystrophy
Typical Development group
Forty-five male subjects were included in the healthy Typical Development (TD) control group and they were assessed for twenty minutes at rest sitting, and then five minutes whilst performing the maze task on a computer
Behavioral: Typical Development group
Assessment of heart rate variability at rest and during computational task in people with typical Development
- Heart Rate Variability behavior during computational task [ Time Frame: 1 day ]Linear, non-linear and complexity indices of heart rate variability will be assessed at rest and during computational task, in order to analyse it's behavior.
To learn more about this study, you or your doctor may contact the study research staff using the contact information provided by the sponsor.
Please refer to this study by its ClinicalTrials.gov identifier (NCT number): NCT04607824
|Comitê de ética da Faculdade de Medicina da Universidade de São Paulo|
|São Paulo, SP, Brazil, 01246903|
|Principal Investigator:||Carlos BM Monteiro, Ph.D.||University of Sao Paulo|