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The Quebec User Evaluation of Satisfaction with Assistive Technology (QUEST 20): An overview of recent progress

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Abstract

. The Quebec User Evaluation of Satisfaction with Assistive Technology (QUEST 2.0) is a 12-item outcome measure that assesses user satisfaction with two components, Device and Services. Psychometric properties have been tested with respect to test-retest stability. alternate-form equivalence. internal consistency, factorial composition and nomological validity. Examples of results obtained with the first version of the tool in outcome studies in Europe and North America support the importance and relevance of the satisfaction measure.
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... Design factors were based on a modified Quebec User Evaluation of Satisfaction with Assistive Technology (QUEST 2.0). 22 Additional modifications included the removal of "access" for "service" items, changes to the ranking labels from "satisfaction" levels to "level of importance", and item labels were adjusted to better suit actuated devices such as adding mechanical power. Participants would be asked for their opinions and experiences on assistive devices, these open-question responses would undergo thematic analysis to extract additional design factors missed by the QUEST 2.0. ...
... o Occupational Therapist (6) o Orthotist (7) o Physiotherapist (8) o Prosthetist (9) o Rehabilitation Specialist (10) o Other (please specify) (11) Q4: Have you worked in this field within the last 5 years? (11) o MeCFES (12) o Microstim (13) o MyoPro Orthosis (14) o NESS Handmaster (15) o Odstock (16) o PneuGlove (17) o ReHand (18) o ReIn-Hand system (19) o RUPERT (20) o SaeboMAS (21) o SCRIPT Active Orthosis (22) o SEM Glove (23) o SNU Exo-Glove (24) o Tenoexo hand exoskeleton (25) o TENS Stimulator (26) o TIGER (27) o X-Glove (28) o None (29) o Other (please specify) ( (11) o MeCFES (12) o Microstim (13) o MyoPro Orthosis (14) o NESS Handmaster (15) o Odstock (16) o PneuGlove (17) o ReHand (18) o ReIn-Hand system (19) o RUPERT (20) o SaeboMAS (21) o SCRIPT Active Orthosis (22) o SEM Glove (23) o SNU Exo-Glove (24) o Tenoexo hand exoskeleton (25) o TENS Stimulator (26) o TIGER (27) o X-Glove (28) (11) o MeCFES (12) o Microstim (13) o MyoPro Orthosis (14) o NESS Handmaster (15) o Odstock (16) o PneuGlove (17) o ReHand (18) o ReIn-Hand system (19) o RUPERT (20) o SaeboMAS (21) o SCRIPT Active Orthosis (22) o SEM Glove (23) o SNU Exo-Glove (24) o Tenoexo hand exoskeleton (25) o TENS Stimulator (26) o TIGER (27) o X-Glove (28) o Other (please specify) ( (1) Ease of use (2) Mechanical power (3) Portability (4) Safety (5) User satisfaction (6) Wearability and comfort (7) Weight (8) (6) o Graded Redefined Assessment of Strength, Sensibility and Prehension (GRASSP) (7) o Jebsen-Taylor Hand Function tests (JTHFT) (8) o Motor Activity Log (MAL) (9) o Motor Assessment Scale (MAS) (10) o Nine Hole Peg Test (9HPT) (11) o Pain (self-reported) (12) o Purdue Pegboard test (PPT) (13) o Range of Motion tests (14) o Southampton Hand Assessment Procedure (SHAP) (15) o Wolf Motor Function Test (WMFT) (16) o Other (please specify) (17) _______________________________________________ (6) o Graded Redefined Assessment of Strength, Sensibility and Prehension (GRASSP) (7) o Jebsen-Taylor Hand Function tests (JTHFT) (8) o Motor Activity Log (MAL) (9) o Motor Assessment Scale (MAS) (10) o Nine Hole Peg Test (9HPT) (11) o Pain (self-reported) (12) o Purdue Pegboard test (PPT) (13) o Range of Motion tests (14) o Southampton Hand Assessment Procedure (SHAP) (15) o Wolf Motor Function Test (WMFT) (16) o None (17) o Other (please specify) (18) Q21: What do you feel are the main limitations to assessing outcomes for patients requiring hand and wrist assistive devices? ...
... o Occupational Therapist (6) o Orthotist (7) o Physiotherapist (8) o Prosthetist (9) o Rehabilitation Specialist (10) o Other (please specify) (11) Q4: Have you worked in this field within the last 5 years? (11) o MeCFES (12) o Microstim (13) o MyoPro Orthosis (14) o NESS Handmaster (15) o Odstock (16) o PneuGlove (17) o ReHand (18) o ReIn-Hand system (19) o RUPERT (20) o SaeboMAS (21) o SCRIPT Active Orthosis (22) o SEM Glove (23) o SNU Exo-Glove (24) o Tenoexo hand exoskeleton (25) o TENS Stimulator (26) o TIGER (27) o X-Glove (28) o None (29) o Other (please specify) ( (11) o MeCFES (12) o Microstim (13) o MyoPro Orthosis (14) o NESS Handmaster (15) o Odstock (16) o PneuGlove (17) o ReHand (18) o ReIn-Hand system (19) o RUPERT (20) o SaeboMAS (21) o SCRIPT Active Orthosis (22) o SEM Glove (23) o SNU Exo-Glove (24) o Tenoexo hand exoskeleton (25) o TENS Stimulator (26) o TIGER (27) o X-Glove (28) (11) o MeCFES (12) o Microstim (13) o MyoPro Orthosis (14) o NESS Handmaster (15) o Odstock (16) o PneuGlove (17) o ReHand (18) o ReIn-Hand system (19) o RUPERT (20) o SaeboMAS (21) o SCRIPT Active Orthosis (22) o SEM Glove (23) o SNU Exo-Glove (24) o Tenoexo hand exoskeleton (25) o TENS Stimulator (26) o TIGER (27) o X-Glove (28) o Other (please specify) ( (1) Ease of use (2) Mechanical power (3) Portability (4) Safety (5) User satisfaction (6) Wearability and comfort (7) Weight (8) (6) o Graded Redefined Assessment of Strength, Sensibility and Prehension (GRASSP) (7) o Jebsen-Taylor Hand Function tests (JTHFT) (8) o Motor Activity Log (MAL) (9) o Motor Assessment Scale (MAS) (10) o Nine Hole Peg Test (9HPT) (11) o Pain (self-reported) (12) o Purdue Pegboard test (PPT) (13) o Range of Motion tests (14) o Southampton Hand Assessment Procedure (SHAP) (15) o Wolf Motor Function Test (WMFT) (16) o Other (please specify) (17) _______________________________________________ (6) o Graded Redefined Assessment of Strength, Sensibility and Prehension (GRASSP) (7) o Jebsen-Taylor Hand Function tests (JTHFT) (8) o Motor Activity Log (MAL) (9) o Motor Assessment Scale (MAS) (10) o Nine Hole Peg Test (9HPT) (11) o Pain (self-reported) (12) o Purdue Pegboard test (PPT) (13) o Range of Motion tests (14) o Southampton Hand Assessment Procedure (SHAP) (15) o Wolf Motor Function Test (WMFT) (16) o None (17) o Other (please specify) (18) Q21: What do you feel are the main limitations to assessing outcomes for patients requiring hand and wrist assistive devices? ...
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... This ensured the IMTIs were adapted to users' needs and tasks, minimizing any negative usage outcomes (Paredes et al., 2013). Building upon the student prototypes, four durable IMTIs were developed and three of them evaluated in a realistic setting with 30 participants to examine both usabilitye.g., learnability, efficiency and ease of use (using the system usability scale -SUSdeveloped by Brooke (1995)), and satisfactione.g., safety, durability, tangibility (using the Quebec user evaluation of satisfaction with assistive technology -QUESTquestionnaire developed by Demers et al. (2002)). ...
... User Satisfaction: Building on the Quebec user evaluation of satisfaction with assistive technology (QUEST) questionnaire (Demers et al., 2002), seven additional user satisfaction questions (AUSQ) were composed and used to assess participant satisfaction with the IMTI on a five-point Likert scale (higher score = higher satisfaction). ...
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... To evaluate the wearability of the exoglove, we asked the hemiplegic patients to perform donning and doffing of the prototyped glove three times each and complete the Quebec user evaluation of satisfaction with assistive technology (QUEST 2.0) on a five-point Likert scale (Demers et al., 2002). Of the 12 items in QUEST 2.0, we retrieved the eight items concerning assistive devices and used them for subjective evaluation. ...
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We developed the knitted shape-memory alloy (SMA) as a flexible actuator and applied it to a soft wearable exoglove for rehabilitation assistance. Based on user needs and anthropometric data, we custom-designed the exoglove for three hemiplegic patients using the knitted-SMA actuator and evaluated its bending performance, gripping force and wearability under the four simulation conditions (S1–S4). To address the specific needs, both SMA plain- and double-knit modules were applied to the exoglove based on the patients’ finger joint range of motion (ROMs). The joint ROMs of all fingers increased by 13.71% and the skin temperature increased by 2.21 °C after actuating the glove ( p = 0.006). The gripping force increased as much as 55.01%, when compared to the baseline. All patients were able to don and doff the developed glove independently, and positively evaluated their subjective satisfaction and thermal perception. The findings suggested the potential of the knitted SMA for the future development of soft wearable robots.
... 38 This range goes from 6 (''not effort at all'') to 20 (''absolute maximal effort, exhaustion''), and it was used as an indicator to terminate the experimental session if the level perceived was close to the maximum. In addition, after the last experimental session, patients filled two questionnaires: NASA Task Load Index (NASA-TLX) 39 that estimated the perceived mental workload; and Quebec User Evaluation of Satisfaction with Assistive Technology (QUEST 20) 40 that evaluated the satisfaction with the exoskeleton. ...
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This study explores the use of a brain-computer interface (BCI) based on motor imagery (MI) for the control of a lower limb exoskeleton to aid in motor recovery after a neural injury. The BCI was evaluated in ten able-bodied subjects and two patients with spinal cord injuries. Five able-bodied subjects underwent a virtual reality (VR) training session to accelerate training with the BCI. Results from this group were compared with a control group of five able-bodied subjects, and it was found that the employment of shorter training by VR did not reduce the effectiveness of the BCI and even improved it in some cases. Patients gave positive feedback about the system and were able to handle experimental sessions without reaching high levels of physical and mental exertion. These results are promising for the inclusion of BCI in rehabilitation programs, and future research should investigate the potential of the MI-based BCI system.
... capturing the full breadth of users' perspectives. 19,[37][38][39][40] Additionally, the use of patient reported outcome measures in foot and ankle research are rarely used consistently. 41 Future studies should examine ways to improve patient-reported outcome measures by expanding the frequency of inquiries regarding expressive, aesthetic, and accessibility concerns of device users. ...
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... It provides a level from 1 to 10. In addition, user satisfaction with the exoskeleton H3 was assessed with the Quebec User Evaluation of Satisfaction with Assistive Technology (QUEST 20) [7]. This questionnaire evaluated user satisfaction based on different characteristics of the assistive device. ...
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Purpose: We aimed to evaluate the applicability of the newly developed joint angle measurement system consisting of six-axis inertial measurement unit sensors and tablet-based application that measure and store angular velocity and acceleration data for estimating joint angles. Materials and Methods: The tablet-based application was used to calculate the orientation angles from angular velocity and acceleration data measured using a single sensor. The relative angles were calculated using the data from multiple sensors. In experiment 1, the validity and reliability of calculated angles was examined using a test device. In experiment 2, the angles of five joints were calculated in four healthy participants using attached inertial measurement unit sensors; the angles were compared with universal goniometer-measured values. In experiment 3, usability and satisfaction were evaluated with the System Usability Scale (SUS) and a Quebec User Evaluation of Satisfaction with Assistive Technology (QUEST)-like scale. Results: In experiment 1, the mean difference of the time-series data between those obtained by the developed system and test device was <0.2 degree for all axes. In experiment 2, the mean difference of the integrated data was 0.2 degree. The mean difference for all joints was <5 degree, indicating that the measurement system is comparable to the universal goniometer. In experiment 3, the median SUS and QUEST-like scale scores were 81 and 4.0, respectively, indicating high usability and satisfaction. Conclusion: The newly developed joint angle measurement system has high accuracy in measuring angles and sufficient validity in application to human joint angles, with high usability and user satisfaction.
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Background Tetraplegia imposes significant challenges on affected individuals, caregivers, and health care systems. Assistive technologies (ATs) such as assistive robotic arms have been shown to improve the quality of life of persons with tetraplegia, fostering independence in daily activities and reducing caregiver burden. Despite potential benefits, the integration of AT innovations into daily life remains difficult. Implementation science offers a systematic approach to bridge this know-do gap. Objective This study aimed to (1) identify and involve relevant stakeholders; (2) identify relevant contextual factors (barriers and facilitators); and (3) suggest a general outlook for the implementation of AT, specifically an assistive robotic arm, into the everyday private lives of individuals with tetraplegia in Switzerland. Methods A qualitative design was used, involving 3 semistructured online focus group interviews with 8 stakeholder groups, including persons with tetraplegia as well as those who could provide perspectives on engineering or technology, legal matters, nursing or care, therapy, social counseling, social insurance, and political considerations. The interviews were analyzed using the Focus Group Illustration Mapping tool, and the data were aligned with the domains of the Consolidated Framework for Implementation Research. Results 3 focus group interviews comprising 22 participants were conducted, and data were mapped onto 21 constructs across the Consolidated Framework for Implementation Research domains. Identified barriers were customization to users’ needs, safety concerns, and financing issues for the high AT costs. The collaboration with different stakeholders, including those who provided perspectives on political engagement, proved crucial. Identified facilitators included the enhancement of autonomy for persons with tetraplegia, improvement of quality of life, reduction of caregiver dependency, and addressing health care labor shortages. The implementation outlook involved the formation of an experienced team and the development of an implementation plan using hybrid type 1 and type 2 designs that incorporate both qualitative and quantitative implementation and innovation outcomes. Conclusions Robotic arms offer promising benefits in terms of improved participation for users, while high costs and regulatory complexities as to who will assume these costs limit their implementation. These findings highlight the complexities involved in implementing AT innovations and the importance of addressing contextual factors. A specific framework for the implementation of AT is needed to ensure the successful integration in Switzerland and other countries with comparable social and health insurance systems.
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Background and Objective Personal wheelchair budgets (PWBs) are offered to everyone in England eligible for an NHS wheelchair, to support their choice of equipment. The WATCh (Wheelchair outcomes Assessment Tool for Children) and related WATCh-Ad tool for adults are patient centred outcomes measures (PCOMs) developed to help individual users express their main outcome needs when obtaining a wheelchair and rate their satisfaction with subsequent outcomes after receiving their equipment. We explored their use in a real-world setting, aiming to produce guidance for use alongside the PWB process. Methods Three wheelchair service provider organisations across four sites participated. Staff and users completed surveys about their experience of the WATCh and/or WATCh-Ad tools used in the assessments. Towards the end of the study, selected patients were interviewed after receipt of their equipment, and staff were interviewed after experiencing a number of assessments. Thematic analysis was undertaken using the tool, survey and interview data. Results Information on 75 assessments by 15 staff was obtained. Over three-quarters of users or their carers rated the use of the tools in the assessment process as ‘helpful’ or ‘very helpful’. Staff reported that use of the WATCh tools had been considered ‘useful’ in developing individual care plans in around 1 in 3 cases and affected the prescription in 1 in 4 cases. Concerns were expressed around the length of time taken to administer the tools in clinic, although some staff noted this reduced with more hands-on experience, and by providing the tools to users in advance of the appointment. Conclusions The WATCh and WATCh-Ad PCOM tools are suitable for routine use by wheelchair service providers to assist the assessment process. It is recommended that tool materials are provided in advance to users/carers, and that staff are allowed time to develop their ways of working with them.
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The purpose of this study was to evaluate user satisfaction with wheelchair seating aids. A modified version of the Quebec User Evaluation of Satisfaction with assistive Technology (QUEST) was used to assess satisfaction of 24 subjects who owned a modular-type seating device integrated in a powered wheelchair. The results of this QUEST-based approach revealed that the variable comfort was identified as the most important consumer criterion yet it was evaluated as the least satisfying. There were statistically significant (p < 0.05) gender differences in the degree of importance and the degree of satisfaction scored on several variables as well as significant differences between subjects living at home and subjects living in institutions. The results support the value of consumer opinion and challenge the assumptions of assistive technology professionals. This study underscores the appropriateness of assessing consumer satisfaction in a systematic and ecologically valid manner.
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Assistive devices (ADs) are considered essential to the health and well-being of all people but especially people with sensory or physical disabilities. These include such products as wheelchairs, low vision aids, prosthetic limbs, and hearing aids. Since current quality of life measures are inadequate for assessing the impact of ADs, a questionnaire to measure the psychosocial impact of ADs on users was developed and standardized. Factor analysis yielded three factors. This led to the creation of three subscales that measure the impact along the domains of competence, adaptability, and self-esteem. The results show that the scales have good reliability. To examine utility, the scales were used to compare two competing ADs - eyeglasses and contact lenses. These results show that the subscales have good validity. Clinical studies are now in progress.
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The Quebec User Evaluation of Satisfaction with assistive Technology (QUEST) is an outcome assessment tool designed to identify the sources of user satisfaction and dissatisfaction with assistive technology. This paper presents the results of an international content validation study of the QUEST that was conducted as part of the ongoing development of this assessment instrument. A questionnaire developed to measure the relevance of QUEST items and to critique the administration procedures was completed by an international group of 12 assistive technology experts from the United States, the Netherlands and Canada. At the test level, the findings revealed that the QUEST was adequately sampled in terms of embracing all the important facets of satisfaction with assistive technology. At the item level, however, it was revealed that changes needed to be made to the wording of the satisfaction variables and to the administration procedures for the QUEST in order to ensure optimal content validity. A limitation of the study is the heterogeneity of the testing sites that may have reduced the chances of reaching consensual agreement among the content experts. It is recommended that future studies consider alternative methods such as factorial analysis to support the findings of this study. Copyright © 1999 Whurr Publishers Ltd.
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Includes bibliographical references (leaves 100-103). Thesis (M.S.)--University of Pittsburgh, 2000. Graduate School of Public Health.
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Many applied health service researchers launch into patient satisfaction surveys without realizing the complexity of the task. This paper identifies the difficulties involved in executing patient satisfaction surveys. The recent revival of interest in 'satisfaction' and disagreements over the meaningfulness of a unitary concept itself are outlined, and the various perspectives and definitions of the components of satisfaction are explored. The difficulties of developing a comprehensive conceptual model are considered, and the issues involved in designing patient satisfaction surveys--and the disasters that occur when these issues are ignored--are then set out. The potential cost-effectiveness of qualitative techniques is discussed, and the paper concludes by discussing how health care management systems could more effectively absorb the findings of patient satisfaction surveys.
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The paper aims at answering the question: Has the measurement of patient satisfaction improved the quality of care? After concluding that there is no evidence in the literature, the paper proceeds to look at why the evidence is lacking. Four factors seem to explain it: the objectives, the focus and the originator of the patients satisfaction studies and measurements and difficulties related to the interpretation of the findings. The last part of the paper analyses why patient satisfaction should be taken seriously although we do not know whether its measurement improves the quality of care. They include the fact that the patients are partners in health care; they literally feel in their skin whether care is good or bad. They are also the best judges of certain aspects of care, such as amenities and interpersonal relations. The second reason is the transformation of health care from a sellers' market to a consumers' market where the satisfaction of the patients' needs is part of the definition of quality. Finally, there is the ideological reason that, in a democratic society, the patients should have the right to influence decisions and activities influencing them. Measurement of patient satisfaction realizes the principle of community participation in health care.