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StrokeNCT04657029

Aerobic Exercise and Sensorimotor Adaptation in Chronic Stroke

A study testing Treadmill in people with Stroke, run by The University of Queensland at 1 site in Australia.

Completed

Finished. The study has ended and is not enrolling. Results may be posted on the official record.

Official record
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Trial summary

A single-blinded crossover study. Participants attended two separate sessions at the university campus, completing an aerobic exercise intervention in one session and a resting control condition in the other session. Sensorimotor adaptation was assessed before and after each session. Read more about this study

Who is it for?
Any age
Conditions the study is for
Stroke
What is being tested?
Treadmill
Could I receive a placebo?
No, everyone receives an active treatment
How many people
20 participants
Where
1 siteAustralia
Study dates
1 Jun 2017to 1 Mar 2020
Phase
Interventional
Are there results?
None posted in the registry

Key requirements

Who can take part, as listed by the sponsor. Only the study team can confirm whether you are eligible, so take this list to your doctor.

  • Ages Any age
  • All sexes
  • No healthy volunteers
  • Child, Adult, Older adult

Who may be able to join

  • Clinical diagnosis of stroke
  • Time of stroke greater than three months ago
  • Be able to walk with or without and aid for at least 10 metres
  • Understand three stage commands

Who cannot join

  • Unable to walk independently prior to current stroke
  • Have co-morbidities that limit their walking (e.g. arthritis, orthopaedic surgery)
  • Unstable cardiac status
  • Unable to understand three stage commands
  • Unable to provide informed consent

Trial locations and contacts

1 site in 1 country.

Australia1 site
  • The University of Queensland

    Brisbane, Queensland, 4072

Other trials in Australia

About this study

Official title: The Acute Effects of Aerobic Exercise on Sensorimotor Adaptation in Chronic Stroke

A single-blinded crossover study. Participants attended two separate sessions at the university campus, completing an aerobic exercise intervention in one session and a resting control condition in the other session. Sensorimotor adaptation was assessed before and after each session. Participants were twenty people with chronic stroke. Intervention completed was treadmill exercise at mod-high intensity for 30 minutes.

Read the detailed description

Participants Twenty people with chronic stroke participated in the study (aged 61 ± 13 years; 76% male).

Experimental design In a cross-over design, each participant was pseudo-randomised to complete an intervention condition (Treadmill) or control condition (Rest) first, returning at least one week later (washout period) to complete the alternate condition. A minimum washout period of one week was used to allow for any physiological changes due to exercise to return to resting levels, but to minimise any stroke recovery-associated changes to function. Participants were asked to refrain from exercising in the 24 hours prior to their visit. At each visit, participants completed the sensorimotor adaptation task on two occasions, pre and post intervention, resulting in four assessment timepoints (PreControl, PostControl and PreTreadmill, PostTreadmill). The post intervention assessment aimed to commence within 15 minutes of completing the treadmill or rest condition.

Intervention The intervention condition consisted of a single session of moderate-high intensity aerobic exercise (65% of heart rate reserve) for 30 minutes walking on a standard treadmill (Landice L7 treadmill), with arms placed comfortably by participants on the rail (in front) or swinging freely. Information describing the specific features of the training session (e.g. heart rate, blood pressure response, treadmill speed, total distance walked) were recorded to monitor the response to exercise and adherence to the exercise protocol. The single treadmill session included a progressive increase in intensity (usually increased speed, or gradient) to reach the target heart rate (approx. 5 mins) as well as a cooling down period (approx. 5 mins) to allow for participants to return towards resting levels for vital observations. The warm-up and cool-down were included as part of the total 30 minutes of walking exercise. Target heart rates were calculated using the Karvonen method with levels adjusted for those taking heart rate lowering medications (i.e. beta blockers), following methods previously published in post stroke populations. Heart rate was measured using a chest strap monitor (polar-electro) and monitored by a research assistant who facilitated changes in treadmill parameters to enable participants to reach their target. Participants were asked to self-rate their intensity of exercise every 10 minutes verbally using BORG's 6-20 scale rating of perceived exertion. Participants were instructed to walk at a pace that resulted in a rating between 11 (fairly light) and 14 (somewhat hard) on the scale. The control condition involved an equivalent time period (30 minutes) of seated resting where participants were provided with an education session about the impact and effects of stroke by the same research assistant.

Sensorimotor adaptation task Apparatus and setup. Participants were seated in front of a desk (approximately 50 cm from their coronal plane) and asked to move a digitising pen (15.95 cm long, 1.4 cm wide, 17 g) on a digitizing tablet (WACOM Intuos4 PTK 1240, size: 19.2 x 12 in., resolution = 0.25 mm) from an origin to a target point. The pen's position on the tablet (XY coordinates) was sampled at 100 Hz and displayed in real time as a circular cursor with a 5-pixel radius (1.25 mm) on a horizontally placed computer monitor. Direct vision of the hand was prevented by placing the tablet and the hand directly beneath an opaque stand, with the horizontal monitor placed atop the stand.

Task instructions. Participants first received task instructions to move an on-screen cursor from the start to the target, in a straight line, in a single movement, as quickly and as accurately as possible. Further, participants were instructed that the feedback of the movement would be changed from time-to-time, and that participants were to change their movement in response to this change of feedback, whilst keeping movements as straight as possible.

In each trial, the participants' task was to move from the origin location through the target location as quickly and accurately as possible using their dominant upper limb. Targets were presented in one of three locations (210, 225 or 240 degrees from the right horizontal plane) in random order. These target directions were selected such that target-reaching movements involved the horizontal adductors of the shoulder joint. After moving through the target, or past the target, a high-pitched tone sounded to indicate trial completion. Following completion of a trial the origin location was re-displayed immediately and participant directed to repeat task. If the participant did not complete a successful trial, they were directed to return to the origin location and repeat the trial.

First, participants encountered 18 baseline trials under normal (correct) feedback with no rotation. Participants then immediately completed 66 adaptation trials, where the visual feedback on the display monitor was perturbed by rotating it 30 degrees in a clockwise direction (1st testing day) or counter-clockwise direction (2nd testing day). After the adaptation block, to notify participants that the perturbation had been removed, a popup dialog box appeared with the statement "In the next few trials, the disturbance that the computer applied would be removed. Please aim straight to the target." The instructions on-screen were read out by the experimenter to ensure it was understood. This was immediately followed by 6 no-feedback trials. Finally, participants completed 36 washout trials under normal cursor feedback conditions (i.e., no cursor rotation), to return behaviour to an unadapted state.

Data Processing and Analysis Custom scripts written in LabVIEW scored reach directions, which were quantified at the 15th data point (150 milliseconds into the reach), as online movement corrections typically occur after 150 ms into a reach. Trials with reach direction outside a 120 degree range of the target (60 degrees on either side of the target) were discarded as outliers. Trials were binned into cycles of one visit to each of the three targets. The dependent variable was percent adaptation, which quantified reach directions in every cycle relative to the ideal reach direction by calculating reach directions as a percentage of ideal reach directions resulting from perfect adaptation performance. Ideal reach direction was 30 degree clockwise for a 30 degree counter-clockwise rotation, and 30 degrees counter-clockwise for a 30 degree clockwise rotation.

Percent adaptation=100% × (reach direction)/(ideal reach direction)

As observed previously, there was a rapid error reduction phase of reaching where a majority of learning occurred followed by a slower rate of adaptation. Here, as the targets were spaced close together, rapid error reduction occurred in trials 1-9 (i.e., the first three cycles), similar to recent work. At completion of the fourth cycle, adaptation was greater than 70% both before and after the treadmill and control conditions. We thus selected the first three cycles to quantify rapid error reduction.

Individual differences in reach directions at baseline can affect measures of adaptation. Previous methods of accounting for this by subtracting pre-perturbation behaviour from post-perturbation behaviour is more sensitive to noisy baselines and risk of Type 2 error. To account for pre-perturbation baseline biases, we entered percent adaptation averaged from the final three cycles before rotation onset (i.e., percent adaptation in the last five baseline cycles) as covariates in all of our analysis of covariance analyses.

After the adaptation trials, there were two cycles where no feedback was provided to the participant. That is, unlike all previous trials where participants could follow a tracking cursor with their vision, the participants received no real time feedback about where they were reaching. The first no-feedback cycle was taken as a measure of implicit learning, similar to previous work.

Our outcome measures of interest were (1) adaptation performance (2) implicit aftereffects, quantified as reaches that remained adapted despite notification of perturbation removal in the no-feedback block and (3) explicit learning, estimated as the volitional disengagement of adapted behaviour after receiving notification of perturbation removal (i.e., the change in percent adaptation from the mean of the last three adaptation cycles to the first no-feedback cycle after receiving notification that the perturbation was gone), and (4) de-adaptation performance. To evaluate these measures, we ran ANCOVAs with the between-subjects factor Intervention Order (Control First, Treadmill First) and the within-subjects factors: Intervention (Control, Treadmill), Time (Pre-Intervention, Post-Intervention) and (where applicable) Cycles (cycles 1..3), with pre-rotation biases as covariates of no interest (estimated from mean percent adaptation in the last three baseline cycles). Where appropriate, Greenhouse-Geisser corrections were applied. Alpha was set at 0.05. SPSS v24.0 was used for statistical analyses.

Conditions
Stroke
Being tested
Treadmill
Keywords
sensorimotor adaptation, aerobic exercise
Medical subject headings
Stroke

What participants receive

What participants receive. In a randomised study each person is assigned to one group by chance.

  • TreadmillBehavioural

    30 minutes of moderate-high intensity treadmill training.

Study groups in NCT04657029
Study groupRoleWhat they receive
Treadmill conditionExperimentalThe intervention condition consisted of a single session of moderate-high intensity aerobic exercise (65% of heart rate reserve) for 30 minutes walking on a standard treadmill. The single treadmill session included a progressive increase in intensity to reach the target heart rate (approx. 5 mins) as well as a cooling down period (approx. 5 mins). The warm-up and cool-down were included as part of the total 30 minutes of walking exercise. Target heart rates were calculated using the Karvonen method [25] with levels adjusted for those taking heart rate lowering medications (i.e. beta blockers), following methods previously published in post stroke populations [26, 27]. Participants were asked to self-rate their intensity of exercise every 10 minutes verbally using BORG's 6-20 scale rating of perceived exertion [28]. Participants were instructed to walk at a pace that resulted in a rating between 11 (fairly light) and 14 (somewhat hard) on the scale.
Receives: Behavioral: Treadmill
Control conditionOtherThe control condition involved an equivalent time period (30 minutes) of seated resting where participants were provided with an education session about the impact and effects of stroke by the same research assistant.
Receives: Behavioral: Treadmill

What is being measured

The primary outcome is the main question the study is designed to answer.

  1. Sensorimotor adaptation change

    Participants were seated in front of a desk and asked to move a digitising pen on a digitizing tablet from an origin to a target point. The pen's position on the tablet (XY coordinates) was sampled at 100 Hz and displayed in real time as a circular cursor with a 5-pixel radius (1.25 mm) on a horizontally placed computer monitor. Direct vision of the hand was prevented by placing the tablet and the hand directly beneath an opaque stand, with the horizontal monitor placed atop the stand.

    Measured: Pre and Post intervention and Pre and Post Control. There was one week between the two conditions

Timeline

From the start of the study to its completion; the mark is today. Estimated dates are the sponsor’s plan.

  1. First posted8 Dec 2020
  2. Study start1 Jun 2017
  3. Primary completion1 Jul 2019
  4. Study completion1 Mar 2020

Resources

More details

For doctors and researchers: how the study is designed, who runs it, and its registry IDs.

Study design
Study type
Interventional
Phase
Phase N/A
Primary purpose
Treatment
Allocation
Randomised
Intervention model
Crossover
Model description
In a cross-over design, each participant was pseudo-randomised to complete an intervention condition (Treadmill) or control condition (Rest) first, returning at least one week later (washout period) to complete the alternate condition. A minimum washout period of one week was used to allow for any physiological changes due to exercise to return to resting levels, but to minimise any stroke recovery-associated changes to function. Participants were asked to refrain from exercising in the 24 hours prior to their visit. At each visit, participants completed the sensorimotor adaptation task on two occasions, pre and post intervention, resulting in four assessment timepoints (PreControl, PostControl and PreTreadmill, PostTreadmill). The post intervention assessment aimed to commence within 15 minutes of completing the treadmill or rest condition.
Masking
Single blind
Who is masked
Outcomes assessor
Enrolment
20 participants (actual)
IDs, dates and publications
ClinicalTrials.gov ID
NCT04657029
Sponsor's protocol ID
ChrisMackaySensMotStroke2020
Status last verified
Nov 2020
First submitted
22 Nov 2020
Last updated
8 Dec 2020
Results posted
No
Data monitoring committee
No
FDA-regulated drug
No
FDA-regulated device
No
Individual data sharing
No

Publications

  • Neva JL, Ma JA, Orsholits D, Boisgontier MP, Boyd LA. The effects of acute exercise on visuomotor adaptation, learning, and inter-limb transfer. Exp Brain Res. 2019 Apr;237(4):1109-1127. doi: 10.1007/s00221-019-05491-5. Epub 2019 Feb 18.

    PubMed 30778618

Questions about this trial

What is this clinical trial studying?

A study testing Treadmill in people with Stroke, run by The University of Queensland at 1 site in Australia.

The full registered description is in the About this study section and the official record.

Who may be eligible to take part?

The sponsor lists 4 inclusion and 5 exclusion criteria. Eligibility is decided by the study team after screening, so read the full criteria and contact a listed site.

Is this clinical trial currently recruiting?

The record says: finished, as of the sponsor's last update on 8 Dec 2020. Status can change between updates, so confirm with the study contact before making plans.

Where is the study taking place?

The record lists 1 site in Australia. Whether a site is taking part right now should be confirmed with that site. See every site.

What are the possible benefits and risks?

They depend on the study and the treatment, and no study can promise a benefit. The study team explains the known risks during informed consent, before anyone joins; the record itself does not list them.

Are results available for this study?

The study is completed, but results are not available in the source record. That does not mean the treatment did or did not work.

How can a doctor refer a patient or contact the research team?

The record lists no contact. The official record names the sponsor, who can be asked directly. AzTrials does not enrol participants or take referrals.

What does the primary outcome measure?

Sensorimotor adaptation change (time frame: Pre and Post intervention and Pre and Post Control. There was one week between the two conditions). It is what the study was designed to measure, not a finding.

Where can I read the original study information?

On the ClinicalTrials.gov record for NCT04657029, which also lists 1 linked publication.

Does a listing mean the treatment is approved or proven to work?

No. A listing means the study is registered. It does not show that the treatment is safe, works, or is approved by a regulator.

How often is this information updated?

AzTrials copies changed records from ClinicalTrials.gov every night and reloads the whole registry every week. The sponsor last updated this record on 8 Dec 2020.

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Clinical Trial NCT04657029 | AzTrials