Clinical Feasibility of Minimally Supervised Therapy After Stroke With a Hand Rehabilitation Robot

Stroke Clinical Trial

Official title:

Clinical Feasibility of Minimally Supervised Therapy After Stroke With a Hand Rehabilitation Robot (ReHapticKnob): Pilot and Main Study

Clinical Trial Details — Status: Completed

Administrative data

• NCT number: NCT04388891
• Other study ID #: ReHapticKnob 2020
• Status: Completed
• Phase: N/A
• Start date: August 11, 2020
• Est. completion date: September 14, 2023

Study information

• Verified date: February 2024
• Source: Swiss Federal Institute of Technology
• Contact: n/a
• Is FDA regulated: No
• Study type: Interventional

Clinical Trial Summary

The ReHapticKnob is a robot for hand rehabilitation after stroke. We aim to investigate the feasibility of minimally supervised therapy with the ReHapticKnob with stroke patients in a rehabilitation clinic, evaluate the usability of the ReHapticKnob (user interface and implemented exercises which were adapted for independent usage), and quantify the dose of additional robotic therapy that patients perform in a minimally supervised setting.

Minimally supervised therapy means that after a training phase, where the therapists teach to the patients how to perform the exercises with the robot, the patients can autonomously train with the robot during free time without being directly supervised. Our hypothesis is that minimally supervised therapy might be a possible way to increase therapy dose for stroke patients, with the potential to further improve recovery of hand function with minimal additional burden for therapists and for the healthcare system.

Recruitment information / eligibility

• Status: Completed
• Enrollment: 23
• Est. completion date: September 14, 2023
• Est. primary completion date: September 14, 2023
• Accepts healthy volunteers: No
• Gender: All
• Age group: 18 Years to 90 Years

Eligibility

Inclusion Criteria:

• Male and female stroke patients between 18 and 90 years old;

• pre-stroke Modified Rankin Score = 1;

• acute/subacute stroke (within (=) 6 weeks from onset);

• NIHSS = 1 in at least one of the items regarding motor function, sensory functions and ataxia;

• the patient read, understood and signed the informed consent.

Exclusion Criteria:

• Modified Ashworth Scale > 2 for one or more of the following muscles: shoulder adductors, forearm pronator and supinator, flexors and extensors of elbow, wrist and fingers;

• moderate to severe aphasia: Goodglass-Kaplan scale < 3;

• moderate to severe cognitive deficits: levels of cognitive functioning-revised (LCF-R) < 8;

• functional impairment of the upper limb due to other pathologies;

• severe pain in the affected arm: visual analogue scale for pain (VASp) = 5;

• other pathologies which may interfere with the study;

• pacemakers and other active implants.

Related Conditions & MeSH terms

• Stroke

Intervention

Device:
• Minimally supervised therapy with the ReHapticKnob
The therapy with the ReHapticKnob is performed in the clinic in addition to the conventional therapy. During the supervised and semi-supervised phases (first 2 weeks), the intervention dose is 5 sessions of approximately 45 minutes per week. During each session, the robot proposes a set of 3 exercises, each lasting between 10 and 15 minutes. During the minimally supervised phase (third and fourth week), the duration of the ReHapticKnob therapy is not specified, since the patient can decide by him/herself when to use the device, e.g. during freetime or during the weekend.

Locations

Country	Name	City	State
Switzerland	Clinica Hildebrand Centro di riabiliazione Brissago	Brissago	Ticino

Sponsors (3)

Lead Sponsor	Collaborator
Swiss Federal Institute of Technology	CLINICA HILDEBRAND CENTRO DI RIABILITAZIONE BRISSAGO, Rehabilitation Engineering Laboratory, ETHZ

Country where clinical trial is conducted

Switzerland, 

Outcome

Type	Measure	Description	Time frame	Safety issue
Primary	Compliance as assessed by dose	Sum of the dose of robot-assisted therapy without direct supervision that the patient performs.	Compliance to minimally supervised therapy is calculated at the end of the fourth week of the study protocol.
Secondary	Usability as assessed by the Post-Study System Usability Questionnaire	Usability of the ReHapticKnob measured with the Post-Study System Usability Questionnaire (version 3). This questionnaire consists of 16 questions and the possible response options vary between 1 (strongly agree) and 7 (strongly disagree).	Usability is first measured at the end of the second week.
Secondary	Usability as assessed by the Post-Study System Usability Questionnaire	Usability of the ReHapticKnob measured with the Post-Study System Usability Questionnaire (version 3). This questionnaire consists of 16 questions and the possible response options vary between 1 (strongly agree) and 7 (strongly disagree).	Usability is measured again at the end of the fourth week.
Secondary	Usability as assessed by the System Usability Scale	Usability of the ReHapticKnob measured with the System Usability Scale. The possible response options vary between 1 (strongly disagree) and 5 (strongly agree).	Usability is first measured at the end of the second week.
Secondary	Usability as assessed by the System Usability Scale	Usability of the ReHapticKnob measured with the System Usability Scale. The possible response options vary between 1 (strongly disagree) and 5 (strongly agree).	Usability is measured again at the end of the fourth week.
Secondary	Usability as assessed by the NASA Task Load Index	Usability of the ReHapticKnob measured with the NASA Task Load Index.	Usability is first measured at the end of the second week.
Secondary	Usability as assessed by the NASA Task Load Index	Usability of the ReHapticKnob measured with the NASA Task Load Index.	Usability is measured again at the end of the fourth week.
Secondary	Evolution of patient's satisfaction with robot-assisted therapy as assessed by a 5-point scale	A 5-point scale is presented by the robot at the end of each therapy session to measure patient's satisfaction with robot-assisted therapy.	First to fourth week.
Secondary	Change in upper limb functions as assessed by the Fugl-Meyer Assessment of Upper Extremities (FMA-UE)	Change between baseline (i.e. beginning of the study) and final (i.e. end of the study) upper limb functions as assessed by the FMA-UE.	Baseline functions are assessed at the beginning of the first week, final functions are assessed at the end of the fourth week.
Secondary	Change in upper limb functions as assessed by the ABILHAND	Change between baseline (i.e. beginning of the study) and final (i.e. end of the study) upper limb functions as assessed by the ABILHAND scale.	Baseline functions are assessed at the beginning of the first week, final functions are assessed at the end of the fourth week.
Secondary	Change in upper limb functions as assessed by the Box and Block (BBT) test	Change between baseline (i.e. beginning of the study) and final (i.e. end of the study) upper limb functions as assessed by the BBT test.	Baseline functions are assessed at the beginning of the first week, final functions are assessed at the end of the fourth week.
Secondary	Change in upper limb functions as assessed by the Motor Evaluation Scale for Upper Extremities in Stroke Patients (MESUPES)	Change between baseline (i.e. beginning of the study) and final (i.e. end of the study) upper limb functions as assessed by the MESUPES. The scores can vary between 0 and 58, and a higher score means a better outcome.	Baseline functions are assessed at the beginning of the first week, final functions are assessed at the end of the fourth week.
Secondary	Change in upper limb functions as assessed by the modified Ashworth Scale (mAS)	Change between baseline (i.e. beginning of the study) and final (i.e. end of the study) upper limb functions as assessed by the mAS.	Baseline functions are assessed at the beginning of the first week, final functions are assessed at the end of the fourth week.
Secondary	Change in the active Range of Motion (aROM) for grasping as assessed by a custom robotic assessment	Change between baseline (i.e. beginning of the study) and final (i.e. end of the study) aROM for grasping, i.e. for hand opening and closing. This is measured by the robot with a custom assessment.	Baseline aROM is assessed at the beginning of the first week, final aROM is assessed at the end of the fourth week.
Secondary	Change in the active Range of Motion (aROM) for forearm rotation as assessed by a custom robotic assessment	Change between baseline (i.e. beginning of the study) and final (i.e. end of the study) aROM for forearm pronation and supination. This is measured by the robot with a custom assessment.	Baseline aROM is assessed at the beginning of the first week, final aROM is assessed at the end of the fourth week.
Secondary	Change in hand proprioception as assessed by a custom robotic assessment measuring the minimum difference in length that a patient can perceive	Change between baseline (i.e. beginning of the study) and final (i.e. end of the study) hand proprioception, defined as the minimum difference in length that a patient can perceive (i.e. just noticeable difference). This is measured by the robot with a custom assessment.	The baseline assessment is performed at the beginning of the first week, the final assessment is performed at the end of the fourth week.
Secondary	Change in haptic perception as assessed by a custom robotic assessment measuring the minimum difference in stiffness that a patient can perceive	Change between baseline (i.e. beginning of the study) and final (i.e. end of the study) haptic perception, defined as the minimum difference in stiffness that a patient can perceive. This is measured by the robot with a custom assessment.	The baseline assessment is performed at the beginning of the first week, the final assessment is performed at the end of the fourth week.
Secondary	Monitoring of muscle tone	Muscle tone will be monitored throughout the robot-assisted therapy with assessments embedded in some of the exercises implemented in the ReHapticKnob.	First to fourth week.
Secondary	Change in knowledge about stroke and health as assessed by a custom questionnaire consisting of 20 open or multiple-choice questions about stroke and health	Change between baseline (i.e. beginning of the study) and final (i.e. end of the study) knowledge about stroke and health, defined as the number of correct answers out of total number of questions asked about stroke and health. The questionnaire with the 20 questions about stroke and health is custom made.	The baseline assessment is performed at the beginning of the first week, the final assessment is performed at the end of the fourth week.