search
Back to results

Retaining Short-term Training Effects on Gait Adaptability in People With Stroke (ATTAINS)

Primary Purpose

Stroke

Status
Not yet recruiting
Phase
Not Applicable
Locations
Netherlands
Study Type
Interventional
Intervention
Gait adaptability training
Home-based exercise training
Sponsored by
Sint Maartenskliniek
About
Eligibility
Locations
Arms
Outcomes
Full info

About this trial

This is an interventional treatment trial for Stroke

Eligibility Criteria

18 Years - undefined (Adult, Older Adult)All SexesDoes not accept healthy volunteers

Inclusion Criteria: > 6 months after first unilateral supratentorial stroke (chronic phase) Able to walk at least 10 minutes independently Initial involvement of the lower extremity after stroke. Having completed (minimal 8/10 training sessions) the 5 week gait adaptability training program using the C-Mill Exclusion Criteria: Any other neurological or musculoskeletal disease affecting gait or balance (e.g. Parkinson's disease, knee osteoarthritis) Contractures or spasticity requiring other treatment (e.g. botulinum toxin treatment) within the duration of the training period. Severe cognitive or visuo-spatial impairments limiting comprehension of instructions or correct perception of the environments

Sites / Locations

  • Sint Maartenskliniek

Arms of the Study

Arm 1

Arm 2

Arm 3

Arm Type

Experimental

Experimental

No Intervention

Arm Label

Booster group

Home-based exercise group

Control group

Arm Description

Participants assigned to the booster group will receive a three single training sessions 3 months apart targeting gait adaptability using the C-mill. Assessments will take place after giving informed consent which is indicated as the start of the study (baseline), 6 months and 12 months post-baseline.

Participants assigned to the home-based exercise group will receive a program for training at home aiming at a minimum training time of 60 minutes per week. Assessments will take place after giving informed consent which is indicated as the start of the study (baseline), 6 months and 12 months post-baseline

Participants assigned to the control group will not follow any additional intervention other than the standard care they already receive for the year following the completion of the 5-week gait adaptability training using the C-Mill from the ATTAINS study. Assessments will take place after giving informed consent which is indicated as the start of the study(baseline), 6 months and 12 months post-baseline.

Outcomes

Primary Outcome Measures

Walking Adaptability Ladder Test (WALT) score
Measure of gait adaptability. An adapted version for adults of the Walking Adaptability Laddertest for Kids (WAL-K) to assess the ability to flexibly adjust the gait pattern during overground walking. Outcome is based on performance time and foot placement errors measured in seconds where a lower score is a better outcome.
Emory Functional Ambulation Profile (EFAP) score
Measure of gait adaptability. In this task the participants traverse a standardized 5m obstacle course. Outcome is time to perform the task measured in seconds where a lower score is a better outcome

Secondary Outcome Measures

Lab-based walking adaptability test
Measure of gait adaptability. Target stepping task using the Gait Real-time Analysis Interactive Lab (GRAIL) where participant must step on projected stepping stones as accurately as possible. Step width and step length between the stepping stones will vary.
Balance performance
Measure of gait stability, measured by the margin of stability (meter) and the center of mass excursion (meter), on treadmill walking with perturbations using the Gait Real-time Analysis Interactive Lab (GRAIL).
Walking performance
Measure of walking ability using the 10meter walktest, measured in seconds where a lower score is a better outcome.
Balance confidence
Evaluating balance confidence using the Activity Balance Scale, measured on a 0% - 100% scale, where a higher score is a better outcome.
Daily life gait performance as assessed by gait quality
Measured by inertial measurement units placed on both feet and the lower back. Analysis through cusomized algorythms.
Daily life walking activity assessed by walking time per day
Average time of walking during the day (minutes) measured in one week using the Activ8.
Health-related quality of life
Evaluating the disability and health-related quality of life after stroke using the Stroke Impact Scale mobility subscale, measure on a 5-point scale ("could not do at all = 1" - "not difficult at all = 5") where a higher score is a better outcome.
Balance performance through MiniBESTest
Measure of balance and gait stability using the Mini Balance Evaluation Systems Test (MiniBESTes). Tasks are score on a 3-point scale. Outcome is an average score ranging between 0 and 1 where a higher score is a better outcome.

Full Information

First Posted
April 11, 2023
Last Updated
April 11, 2023
Sponsor
Sint Maartenskliniek
Collaborators
ZonMw: The Netherlands Organisation for Health Research and Development
search

1. Study Identification

Unique Protocol Identification Number
NCT05825053
Brief Title
Retaining Short-term Training Effects on Gait Adaptability in People With Stroke
Acronym
ATTAINS
Official Title
The Effect of Single Booster Sessions or Home-based Exercise Program for Individuals in the Chronic Phase After Stroke to Retain Short-term Training Effects on Gait Adaptability, a Study-protocol.
Study Type
Interventional

2. Study Status

Record Verification Date
April 2023
Overall Recruitment Status
Not yet recruiting
Study Start Date
April 2023 (Anticipated)
Primary Completion Date
December 2025 (Anticipated)
Study Completion Date
December 2025 (Anticipated)

3. Sponsor/Collaborators

Responsible Party, by Official Title
Sponsor
Name of the Sponsor
Sint Maartenskliniek
Collaborators
ZonMw: The Netherlands Organisation for Health Research and Development

4. Oversight

Studies a U.S. FDA-regulated Drug Product
No
Studies a U.S. FDA-regulated Device Product
No

5. Study Description

Brief Summary
Background: The majority of stroke survivors regain walking ability. However, the ability to adapt gait patterns to meet environmental demands remains impaired in a majority of people in the chronic phase after stroke. This impaired gait adaptability has a profound impact on activities of daily living and quality of life. Treatment targeting gait adaptability is therefore critical for safe and independent community ambulation in people with stroke. Augmented or virtual reality in rehabilitation programs can be used to train gait adaptability in a controlled situation. A few studies have evaluated gait adaptability training in people with stroke. Although results were promising, these studies did not include an adaptability-related outcome measure, or were limited to uncontrolled or small-scaled pilot studies. Moreover, it is unknown if beneficial training effects can be fostered for 1 year after completion of a training program. We evaluate the short-term effects of a 5-week gait adaptability training in an adequately powered, waiting-list controlled clinical trial [ref naar clin trial nummer]. In the current study, we focus on the retention of potentially beneficial effects of this 5 week gait adaptability training program. We will evaluate if short-term effects of gait adaptability training can be retained through single training sessions to boost performance, or by an home exercise program. We hypothesize that booster sessions and home-based exercise will both yield better retention of training effects at 1 year follow-up as compared to the control arm without an experimental intervention. Objective: The primary objective of this study is to test the hypothesis that retention of training-induced gains in gait adaptability can be fostered by providing booster sessions or by prescribing home-based training. Study design: Explorative randomized study, comparing the effect of 3 1-hr booster training sessions against home-based exercise against no intervention on gait adaptability performance 1 year after completion of a 5-week gait adaptability training program. Study population: Stroke patients in the chronic phase after stroke, who completed the 5-week gait adaptability training using the C-Mill and agreed to continue in this follow-up study. We expect this to be 50-75 participants.

6. Conditions and Keywords

Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Stroke

7. Study Design

Primary Purpose
Treatment
Study Phase
Not Applicable
Interventional Study Model
Parallel Assignment
Masking
Outcomes Assessor
Allocation
Randomized
Enrollment
75 (Anticipated)

8. Arms, Groups, and Interventions

Arm Title
Booster group
Arm Type
Experimental
Arm Description
Participants assigned to the booster group will receive a three single training sessions 3 months apart targeting gait adaptability using the C-mill. Assessments will take place after giving informed consent which is indicated as the start of the study (baseline), 6 months and 12 months post-baseline.
Arm Title
Home-based exercise group
Arm Type
Experimental
Arm Description
Participants assigned to the home-based exercise group will receive a program for training at home aiming at a minimum training time of 60 minutes per week. Assessments will take place after giving informed consent which is indicated as the start of the study (baseline), 6 months and 12 months post-baseline
Arm Title
Control group
Arm Type
No Intervention
Arm Description
Participants assigned to the control group will not follow any additional intervention other than the standard care they already receive for the year following the completion of the 5-week gait adaptability training using the C-Mill from the ATTAINS study. Assessments will take place after giving informed consent which is indicated as the start of the study(baseline), 6 months and 12 months post-baseline.
Intervention Type
Behavioral
Intervention Name(s)
Gait adaptability training
Intervention Description
Over a span of 1 year participants will receive 3 one hour, single sessions at 3, 6 and 9 months following baseline assessment, of gait adaptability training, using the C-mill (an instrumented treadmill with augmented reality). Several aspects of gait adaptability, such as obstacle avoidance, accelerating/decelerating and precision stepping, will be trained.
Intervention Type
Behavioral
Intervention Name(s)
Home-based exercise training
Intervention Description
Participants will receive tailored exercise through an online platform targeting gait adaptability. Participants are instructed to train at a minimum of 60 minutes per week, with a frequency of 2 sessions per week. Participants will be supported through tele-consultations on a monthly basis for the first 3 months and bi-monthly for the remaining time of the study. These consultations are focused on technical support, on ways to ensure training progression and to encourage adherence to the program.
Primary Outcome Measure Information:
Title
Walking Adaptability Ladder Test (WALT) score
Description
Measure of gait adaptability. An adapted version for adults of the Walking Adaptability Laddertest for Kids (WAL-K) to assess the ability to flexibly adjust the gait pattern during overground walking. Outcome is based on performance time and foot placement errors measured in seconds where a lower score is a better outcome.
Time Frame
12 months post-baseline
Title
Emory Functional Ambulation Profile (EFAP) score
Description
Measure of gait adaptability. In this task the participants traverse a standardized 5m obstacle course. Outcome is time to perform the task measured in seconds where a lower score is a better outcome
Time Frame
12 months post-baseline
Secondary Outcome Measure Information:
Title
Lab-based walking adaptability test
Description
Measure of gait adaptability. Target stepping task using the Gait Real-time Analysis Interactive Lab (GRAIL) where participant must step on projected stepping stones as accurately as possible. Step width and step length between the stepping stones will vary.
Time Frame
12 months post-baseline
Title
Balance performance
Description
Measure of gait stability, measured by the margin of stability (meter) and the center of mass excursion (meter), on treadmill walking with perturbations using the Gait Real-time Analysis Interactive Lab (GRAIL).
Time Frame
12 months post-baseline
Title
Walking performance
Description
Measure of walking ability using the 10meter walktest, measured in seconds where a lower score is a better outcome.
Time Frame
12 months post-baseline
Title
Balance confidence
Description
Evaluating balance confidence using the Activity Balance Scale, measured on a 0% - 100% scale, where a higher score is a better outcome.
Time Frame
12 months post-baseline
Title
Daily life gait performance as assessed by gait quality
Description
Measured by inertial measurement units placed on both feet and the lower back. Analysis through cusomized algorythms.
Time Frame
12 months post-baseline
Title
Daily life walking activity assessed by walking time per day
Description
Average time of walking during the day (minutes) measured in one week using the Activ8.
Time Frame
12 months post-baseline
Title
Health-related quality of life
Description
Evaluating the disability and health-related quality of life after stroke using the Stroke Impact Scale mobility subscale, measure on a 5-point scale ("could not do at all = 1" - "not difficult at all = 5") where a higher score is a better outcome.
Time Frame
12 months post-baseline
Title
Balance performance through MiniBESTest
Description
Measure of balance and gait stability using the Mini Balance Evaluation Systems Test (MiniBESTes). Tasks are score on a 3-point scale. Outcome is an average score ranging between 0 and 1 where a higher score is a better outcome.
Time Frame
12 months post-baseline

10. Eligibility

Sex
All
Minimum Age & Unit of Time
18 Years
Accepts Healthy Volunteers
No
Eligibility Criteria
Inclusion Criteria: > 6 months after first unilateral supratentorial stroke (chronic phase) Able to walk at least 10 minutes independently Initial involvement of the lower extremity after stroke. Having completed (minimal 8/10 training sessions) the 5 week gait adaptability training program using the C-Mill Exclusion Criteria: Any other neurological or musculoskeletal disease affecting gait or balance (e.g. Parkinson's disease, knee osteoarthritis) Contractures or spasticity requiring other treatment (e.g. botulinum toxin treatment) within the duration of the training period. Severe cognitive or visuo-spatial impairments limiting comprehension of instructions or correct perception of the environments
Central Contact Person:
First Name & Middle Initial & Last Name or Official Title & Degree
Marijne Nieuwelink, MSc
Phone
024-3272731
Email
m.nieuwelink@maartenskliniek.nl
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
Vivian Weerdesteyn, Prof. dr.
Organizational Affiliation
Sint Maartenskliniek
Official's Role
Principal Investigator
Facility Information:
Facility Name
Sint Maartenskliniek
City
Ubbergen
ZIP/Postal Code
6574NA
Country
Netherlands

12. IPD Sharing Statement

Citations:
PubMed Identifier
32776854
Citation
Kuijpers R, Smulders E, Groen BE, Smits-Engelsman BCM, Nijhuis-Van der Sanden MWG, Weerdesteyn V. Reliability and construct validity of the Walking Adaptability Ladder Test for Kids (WAL-K): a new clinical test for measuring walking adaptability in children. Disabil Rehabil. 2022 Apr;44(8):1489-1497. doi: 10.1080/09638288.2020.1802523. Epub 2020 Aug 10.
Results Reference
background
PubMed Identifier
33915437
Citation
Tuijtelaars J, Roerdink M, Raijmakers B, Nollet F, Brehm MA. Polio survivors have poorer walking adaptability than healthy individuals. Gait Posture. 2021 Jun;87:143-148. doi: 10.1016/j.gaitpost.2021.04.031. Epub 2021 Apr 21.
Results Reference
background
Links:
URL
https://www.maartenskliniek.nl/research-innovation-en/research-innovation-projects/attains-gait-adaptability-training-for-people-after-stroke
Description
The English description of the project on the website of the Sint Maartenskliniek.

Learn more about this trial

Retaining Short-term Training Effects on Gait Adaptability in People With Stroke

We'll reach out to this number within 24 hrs