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Clinical Trial Details — Status: Not yet recruiting

Administrative data

NCT number NCT05825053
Other study ID # NL80178.091.21 / 0996_2
Secondary ID
Status Not yet recruiting
Phase N/A
First received
Last updated
Start date April 2023
Est. completion date December 2025

Study information

Verified date April 2023
Source Sint Maartenskliniek
Contact Marijne Nieuwelink, MSc
Phone 024-3272731
Email m.nieuwelink@maartenskliniek.nl
Is FDA regulated No
Health authority
Study type Interventional

Clinical Trial 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.


Recruitment information / eligibility

Status Not yet recruiting
Enrollment 75
Est. completion date December 2025
Est. primary completion date December 2025
Accepts healthy volunteers No
Gender All
Age group 18 Years and older
Eligibility 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

Study Design


Related Conditions & MeSH terms


Intervention

Behavioral:
Gait adaptability training
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.
Home-based exercise training
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.

Locations

Country Name City State
Netherlands Sint Maartenskliniek Ubbergen

Sponsors (2)

Lead Sponsor Collaborator
Sint Maartenskliniek ZonMw: The Netherlands Organisation for Health Research and Development

Country where clinical trial is conducted

Netherlands, 

References & Publications (2)

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. — View 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. — View Citation

Outcome

Type Measure Description Time frame Safety issue
Primary 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. 12 months post-baseline
Primary 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 12 months post-baseline
Secondary 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. 12 months post-baseline
Secondary 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). 12 months post-baseline
Secondary Walking performance Measure of walking ability using the 10meter walktest, measured in seconds where a lower score is a better outcome. 12 months post-baseline
Secondary Balance confidence Evaluating balance confidence using the Activity Balance Scale, measured on a 0% - 100% scale, where a higher score is a better outcome. 12 months post-baseline
Secondary 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. 12 months post-baseline
Secondary 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. 12 months post-baseline
Secondary 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. 12 months post-baseline
Secondary 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. 12 months post-baseline
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