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Clinical Trials/NCT04333615
NCT04333615
Completed
Not Applicable

Effects of Self-selected Walking Exercise Intensity on Adherence, Functional Capacity and Cardiovascular Risk Indicators in Patients With Peripheral Artery Disease

University of Nove de Julho1 site in 1 country20 target enrollmentStarted: September 1, 2021Last updated:

Overview

Phase
Not Applicable
Status
Completed
Enrollment
20
Locations
1
Primary Endpoint
Cerebral perfusion

Overview

Brief Summary

Although the benefits of supervised walking training in patients with peripheral arterial disease (PAD) and symptoms of intermittent claudication (IC) are well established, one of the main problems found in this type of protocol is low adherence to training, which is possibly related to pain during training. In addition, little is known about the impact of performing exercise with pain on cerebral blood flow and cardiovascular health indicators. Thus, the objective of the present study will be to analyze the acute effects of walking exercise with self-selected intensity on the cardiovascular health indicators of patients with PAD. Therefore, 17 patients with PAD will undergo three experimental sessions: exercise with self-selected intensity, exercise until maximum pain and control. The responses of the cardiovascular variables (heart rate variability, blood pressure, heart rate, arterial stiffness and endothelial function) will be obtained before and after the sessions. In addition, during the session cardiovascular responses (cerebral blood flow, blood pressure and heart rate), perceptual and affective responses, as well as information about the exercises performed during the session will be obtained. The responses before and after exercise will be analyzed using the two-way analysis of variance for repeated measures (ANOVA) and the Newman-Keuls post-hoc test. The value of P <0.05 will be considered significant.

Study Design

Study Type
Interventional
Allocation
Randomized
Intervention Model
Crossover
Primary Purpose
Treatment
Masking
Triple (Participant, Investigator, Outcomes Assessor)

Eligibility Criteria

Ages
40 Years to 90 Years (Adult, Older Adult)
Sex
All
Accepts Healthy Volunteers
No

Inclusion Criteria

  • Peripheral artery disease in one or both limbs (ankle brachial index \<0.9);
  • Claudication symptoms in six-minute walking test;
  • who can walk at least 90 meters without interruption;
  • that have physical conditions to perform the exercise sessions;

Exclusion Criteria

  • do not finish three experimental sessions;

Outcomes

Primary Outcomes

Cerebral perfusion

Time Frame: Change from baseline at 30 minutes after the beginning of the exercise.

The cerebral perfusion at rest will be obtained by a transcranial doppler (TCD, Spencer Technologies, United States). To this end, patients will wear a helmet (Marc 600; Spencer Technologies, United States) capable of bilaterally attaching two 2 MHz ultrasound probes to the temporal window. With a method similar to that of an extracranial doppler, the transcranial doppler is capable of capturing the speeds of brain flows. The flow velocities of the middle cerebral artery will be measured bilaterally for 5 minutes, with patients at rest.

Secondary Outcomes

  • Subjective perceived effort(Change from baseline at 35 minutes after the beginning of the exercise.)
  • Cognitive function 2(Change from baseline at post-intervention, after 1 hour and 10 minutes.)
  • Brachial blood pressure(Change from baseline at 30 minutes after the beginning of the exercise.)
  • Heart rate variability(Change from baseline at post-intervention, after 20 minutes.)
  • Feeling Scale(Change from baseline at 35 minutes after the beginning of the exercise.)
  • Cognitive function(Change from baseline at post-intervention, after 1 hour.)

Investigators

Sponsor Class
Other
Responsible Party
Principal Investigator
Principal Investigator

Raphael Mendes Ritti Dias

Professor

University of Nove de Julho

Study Sites (1)

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