Clinical Trial Details
— Status: Completed
Administrative data
| NCT number |
NCT05102682 |
| Other study ID # |
REC reference: 16/EE/0553 |
| Secondary ID |
|
| Status |
Completed |
| Phase |
Phase 1
|
| First received |
|
| Last updated |
|
| Start date |
March 10, 2017 |
| Est. completion date |
September 12, 2017 |
Study information
| Verified date |
February 2024 |
| Source |
East Kent Hospitals University NHS Foundation Trust |
| Contact |
n/a |
| Is FDA regulated |
No |
| Health authority |
|
| Study type |
Interventional
|
Clinical Trial Summary
Title Prospective, open label, single arm, non-randomized, non-comparative feasibility study
of Rex robot assisted rehabilitation exercise to enhance balance, mobility and upper limb
function in people with Multiple Sclerosis "RAPPER III - MS Objective The objective of this
study is to evaluate the feasibility and safety of the REX Robot when used for rehabilitation
with people who have moderate to severe mobility restrictions due to MS. A secondary
objective of the study is to explore the acceptability of the device to people with MS and
its impact on impairments and functions commonly affected by MS.
Study Sponsor Rex Bionics, Plc. Study Device REX Robotic powered exercise system Primary
Endpoint • Completion of a transfer, stand, balance and walk rehabilitation session.
- Unexpected Serious Adverse Events Secondary Endpoints
- Completion of a transfer, stand, balance and walk rehabilitation program over Six-weeks
- The Number of approached, screened, and eligible potential participants. Reasons for
Ineligibility. (See 'RAPPER III- MS 007 Screening Loss Analysis REV 0 FINAL')
- Functional Ambulation Classification (FAC) 1
- Activities-specific Balance Confidence (ABC) Scale 2
- Modified Falls Efficacy Scale (MFES) 3, 4,
- Multiple Sclerosis Walking scale (MSWS-12) 5
- Multiple Sclerosis Impact scale (MSIS-29) 6
- ARMA (arm activity measure) 7
- Berg Balance Scale 8
- Timed unsupported steady stand (TUSS) 9
- Pain scale questionnaire (Visual Analog Score VAS) 10
- Modified Ashworth Score 11
- Spasticity Impact Scale 12
- Epworth Sleepiness Scale (ESS) questionnaire 13
- EQ-5D Health State Questionnaire 14
Questionnaires may be administered in person, by phone, email or in the post.
Description:
Participant Information Sheet Study title: Rex robot Assisted rehabilitation exercise to
enhance balance, mobility and uPPER limb function in people with Multiple Sclerosis "RAPPER
III - MS"
Rex Bionics are now enrolling for RAPPER III, a 10 patient trial at East Kent University
Hospital foundation Trust.
The study will take place at the following address:
School Of Engineering and Arts, Jennison Building, University of Kent, Canterbury CT2 7NT We
would like to invite you to take part in our research study. Before you decide we would like
you to understand why the research is being done and what it would involve for you. One of
our team will go through the information sheet with you and answer any questions you have.
The objective of this feasibility study is to evaluate the overall device safety when used in
a Clinical Rehabilitation Centre under the supervision of a physician and/or qualified
rehabilitation specialist. The trial can be completed by patients over 6 sessions, each a
week apart. The study will consist of walking in REX Bionics powered exercise device and
completing a variety of therapy exercises the assistance of REX trained therapists. You will
be asked to complete some questionnaires and other tests before the first session, after the
3rd session and finally after your 6th session.
This document is broken into 2 parts Part 1 - tells you the purpose of this study and what to
expect if you take part.
Part 2 - gives you more detailed information about the conduct of the study. Part 1 What is
the purpose of this study?
i) To assess the feasibility and safety of undertaking a neuro-rehabilitation exercise
program using a Rex robotic device within a controlled clinical environment (ease of use for
both user and therapist ii) Investigate the potential to improve balance and walking using
Rex for people with MS iii) Investigate the potential health benefits of this Rex
Rehabilitation program iv) Ascertain whether there might be a measurable impact on upper limb
functional abilities
Why have I been invited? You have been asked to participate in this study because you have a
diagnosis of multiple sclerosis that fits the inclusion criteria of this study. There will be
a number of assessments prior to trialling the device to ensure you fit the criteria to
safely use REX. This is for your own safety.
Do I have to take part? It is up to you to decide to join the study. We will describe the
study and go through the information sheet. If you agree to take part, we will then ask you
sign a consent form. You are free to withdraw at any time, without giving a reason. This
would not affect the standard of care you receive. We are planning to enrol 10 people for
this study.
What will happen to me if I take part? Study Schedule You will be asked to come to the rehab
clinic for 6 sessions. The timing of these sessions vary and more detail is given below. Each
session will be a week apart. Please ensure you wear supportive fitting laced shoes, a pair
of comfortable sporting trousers/track suit bottoms and a light T-Shirt or Similar. If you
have issues with the support structures of your feet you should consider using orthotics to
offer added support. Please raise any concerns you have with your therapist conducting the
research so further information can be provided to you.
- Enrolment - You will be asked some screening questions prior being enrolled in the
study. If you are enrolled, you will be asked to complete 13 outcome measures
(tests/questionnaires) in session 1, 4 questionnaires 2 days after session 3 and finally
all 13 outcome measures (tests/questionnaires) in session 6. (approximately 90 minutes)
- Session 1 - you will be asked to come into the clinic to complete a number of tasks.
(approximately 150 minutes)
Task 1: baseline medical assessment and giving informed consent:
A medical examination will take place along with a discussion around your current medical
conditions and previous medical conditions to determine if you are safe to use REX.
You will be given a patient information sheet and ask to give consent if you would like to be
included in the study. You can withdraw at any time and do not have to give consent if you do
not choose to.
Task 2: Assessment against inclusion criteria:
You will be assessed against a number of different inclusion and exclusion criteria to
determine whether you are appropriate for the study
Task 3: completion of pre-treatment outcome measures and questionnaires:
You will be asked to complete a number of scales and questionnaires. These will be repeated
at the end of the study (during sessions 6). If you have any questions about any of these you
should ask the investigator and the investigator will provide you with enough time and space
to discuss everything. The outcome measures are listed below.
- Activities-specific Balance Confidence (ABC) Scale
- Modified Falls Efficacy Scale (MFES)
- Multiple Sclerosis Walking scale (MSWS-12)
- Multiple Sclerosis Impact scale (MSIS-29)
- ARMA (arm activity measure)
- Berg Balance Scale
- Video of sit to stand and stand to sit (recorded twice )
- Video of walking - timed up and go (3 metres )
- Pain scale questionnaire (Visual Analog Score VAS)
- Modified Ashworth Score
- Epworth Sleepiness Scale (ESS) questionnaire
- EQ-5D Health State Questionnaire Task 4: Measurements, fitment and mobilizing A number
of measurements will be taken to ensure you can safely use and fit the device Once these
have been taken you will be asked to transfer into the device. This will be timed.
On completion of a safe transfer you will be asked to stand up in Rex and walk 3 m, turn
around and come back again, then sit back down on the chair. This will be timed.
Task 5: Exercise prescription The investigator will work with you to determine an appropriate
amount of weights/resistance that should be used for your treatment programs in the
subsequent session.
Session 2: Completion of a prescribed exercise program. (approximately 45 minutes) Task 1:
You will be asked to complete a set number of exercises that should last approximately 45
minutes.
Session 3: completion of a prescribed exercise program. (approximately 45 minutes) Task
Task 2: You will be asked to complete 3 questionnaires 2 days (plus or minus one day for
flexibility with your schedule) after your exercise program. These will be completed over the
phone with the investigator conducting the study. You will be given an envelope with all the
questionnaires in so you have a point of reference. These questionnaires will be:
- Pain scale questionnaire (Visual Analog Score VAS)
- Epworth Sleepiness Scale (ESS) questionnaire You will also be assessed for your level of
spasticity using the Modified Ashworth Score
- Session 4: Completion of a prescribed exercise program. (approximately 60 minutes) Task
1: you will be asked to complete a set number of exercises as you did in the previous
sessions
- Session 5: completion of a prescribed exercise program. (approximately 60 minutes) Task
1: you will be asked to complete a set number of exercises as you did in your previous
sessions Task 2: You will be asked to complete a timed transfer to see if it has got any
quicker since your first session.
- Session 6: Completion of follow up outcome measures and questionnaires. (approximately
90 minutes) Task 1: You will be asked to complete all the same scales and questionnaires
you completed in session 1 to see if there has been any improvement.
If you are unable to make the appointed visits in the time frame above, you will need to
notify your physician or rehabilitation therapist.
What are the possible disadvantages and risk of taking part?
- Accidental injury due to falling
- Skin issues such as bruising and redness
- Complications with you blood pressure
- Risks of breaks or fractures through falling
- Hip subluxation/instability
- Risk of Autonomic Dysreflexia with spinal cord injuries of T6 and above
- Risk of unintended bowel movement due to movement in REX
What are the possible benefits of taking part? You might not get benefits from the study,
however a greater understanding of whether the REX System can be used to rehabilitate
patients with a similar condition will be gained from your participation in this study. This
information may contribute to the development of new treatments for persons with Multiple
Sclerosis.
What if there is a problem? Any complaint about the way you have been dealt with during the
study or any possible harm you might suffer will be addressed. The detailed information on
this will be provided in part 2.
Will the taking part in the study be kept confidential? Yes. The records obtained while you
are in this study as well as related health records will be strictly confidential at all
times under the provisions of the 1998 Data Protection Act, to enable analysis of the study
results. With your permission, you're GP and other doctors who may be treating you will be
notified that you are taking part in this study. Further details are included in part 2.
In case of an adverse event your GP will be contacted and informed.
If the information in part 1 has interested you and you are considering participation, please
read the additional information in part 2 before making any decision.
Part 2:
What if relevant new information becomes available? Sometimes we get new information about
the treatments being studied. If this happens, your local research team will tell you and
discuss whether you should continue in the study. You can withdraw from the study at any
time.
What will happen if I don't want to carry on with the study? Taking part in this research
study is voluntary. You may decide to stop at any time. You should tell the researcher if you
decide to stop, this would not affect the standard of care you receive.
In addition, the researchers, Rex Bionics, or your hospital or clinic may stop you from
taking part in this study at any time:
- if it is in your best clinical interest,
- if you do not follow the study procedures,
- If the study is stopped.
What if there is a problem? If you have a concern about any aspect of this study, you should
ask to speak to the researchers who will do their best to answer your questions. If you
remain unhappy and wish to complain formally, you can do this by contacting Mohammed Sakel
the Chief Investigator for NHS sites at msakel@nhs.net. Alternatively you can contact Mathew
Pepper at matthew.pepper@nhs.net or Karen Saunders at karensaunders1@hotmail.com
Will You Be Paid For Participating In This Research Study?
No. But you will be provided with a 50 pound gift voucher for M&S. Free parking will also be
provided when you attend at the clinic.
What Happens if You Are Injured Or Ill In The Course of this Study?
Where to get help:
If you think you have suffered a research-related injury, you should promptly notify the
Principal Investigator listed in the Contact Information at the end of this form. The
Hospital or Clinic will offer care for research-related injuries, including first aid,
emergency treatment and follow-up care as needed.
Who will pay for the treatment of research related injuries?
If you have side effects from the study treatment, you need to report them to the researcher
and your regular physician, and you will be treated as needed. If you have injuries directly
resulting from the application of the study device or procedures, whether at your health care
provider or another institution, the Sponsor, Rex Bionics will pay for appropriate medical
treatment beyond that covered by your health insurance or other third party or government
programs, at no cost to you. Your study doctor can help you obtain this reimbursement.
Sponsor will not be responsible for deductibles and co-pays.
Authorization to Use and Disclose Protected Health Information Your privacy is important to
us, and we want to protect it as much as possible. By signing the consent form, you authorize
the Hospital or Clinic and the investigators to use and disclose any information created or
collected in the course of your participation in this research protocol. This information
might be in different places, including your original medical record, but we will only
disclose information that is related to this research protocol for the purposes listed below.
This information will be given out for the proper monitoring of the study, checking the
accuracy of study data, analysing the study data, and other purposes necessary for the proper
conduct and reporting of this study. If some of the information is reported in published
medical journals or scientific discussions, it will be done in a way that does not directly
identify you.
This information may be given to other researchers in this study, including those at other
institutions, representatives of the company sponsoring the study, including representatives
in your country or other countries, or private, state or federal government parties or
regulatory authorities in your country and other countries responsible for overseeing this
research. These may include the US Food and Drug Administration, the Office for Human
Research Protections, or other offices in your country within the Department of Health
Information Disclosed to Study Sponsor The study data sent by the study doctor to the sponsor
does not include your name, address, ID number, or other information that directly identifies
you. Instead, the study doctor assigns a code number to the study data and may use your
initials. Some study data sent to the sponsor may contain information that could be used
(perhaps in combination with other information) to identify you (e.g. date of birth). If you
have questions about the specific health information that will be sent to the sponsor, you
should ask the study doctor.
This authorization lasts until the end of the study. The study does not end until all data
has been collected, checked (or audited) and analysed. Sometimes this can be years after your
study visits have ended. For example, this could happen if the results of the study are filed
with a regulatory agency like the local regulatory authorities or US Food and Drug
Administration.
You may stop this authorization at any time by writing to the following address:
Mohamed Sakel Director/Consultant Neurorehabilitation Physician East Kent University NHS FT
hospitals Canterbury UK CT13NG
If you stop authorization, the hospital or Rehab centre may continue to use your information
already collected as part of this study, but will not collect any new information.
If you do not sign this authorization, or later stop authorization, you may not be able to
participate in the study.
What Will Happen to Your Data after?
Your data will be used as described for this study. When the study is done, they may be used
for the purpose of publication, your name or identity will NEVER be revealed.
Who Can Answer Your Questions?
You can call the
Principal Investigator: Mohamed Sakel
Study Coordinator:
Phone: 00447500817652
