Technical Feasibility of Supervision of Stretching Exercises by a Humanoid Robot Coach for Chronic Low Back Pain: The R-COOL Randomized Trial

Author:

Blanchard Agathe123,Nguyen Sao Mai45,Devanne Maxime6,Simonnet Mathieu7,Le Goff-Pronost Myriam3,Rémy-Néris Olivier123ORCID

Affiliation:

1. Physical and Rehabilitation Medicine Department, Brest University Hospital, Brest, France

2. Brest University, Brest, France

3. Laboratory of Medical Imaging Processing (LaTIM), INSERM UMR 1101, Brest, France

4. Rambo Team, IMT Atlantique, Brest, France

5. Flowers Team, U2IS, ENSTA Paris, Institut Polytechnique de Paris & Inria, France

6. IRIMAS, Université Haute Alsace, Mulhouse, France

7. LEGO, IMT Atlantique, Brest, France

Abstract

Adherence to exercise programs for chronic low back pain (CLBP) is a major issue. The R-COOL feasibility study evaluated humanoid robot supervision of exercise for CLBP. Aims are as follows: (1) compare stretching sessions between the robot and a physiotherapist (control), (2) compare clinical outcomes between groups, and (3) evaluate participant perceptions of usability and satisfaction and therapist acceptability of the robot system. Prospective, randomized, controlled, single-blind, 2-centre study comparing a 3-week (3 hours/day, 5 days/week) physical activity program. Stretching sessions (30 minutes/day) were supervised by a physiotherapist (control) or the robot. Primary outcome: daily physical activity time (adherence). Secondary outcomes: lumbar pain, disability and fear and beliefs, participant perception of usability (system usability scale) and satisfaction, and physiotherapist acceptability (technology acceptance model). Clinical outcomes were compared between groups with a Student t -test and perceptions with a Wilcoxon test. Data from 27 participants were analysed ( n = 15 control and n = 12 robot group). Daily physical activity time did not differ between groups, but adherence declined (number of movements performed with the robot decreased from 82% in the first week to 72% in the second and 47% in the third). None of the clinical outcomes differed between groups. The median system usability scale score was lower in the robot group: 58 (IQR 11.8) points vs. 87 (IQR 9.4) in the control group at 3 weeks ( p < 0.001 ). Median physiotherapist rating of the technology acceptance model was <3 points, suggesting a negative opinion of the robot. In conclusion, adherence to robot exercise reduced over time; however, lumbar pain, disability, or fear and beliefs did not differ between groups. The results of the participant questionnaires showed that they were willing to use such a system, although several technical issues suggested the KERAAL system could be improved to provide fully autonomous supervision of physical activity sessions.

Funder

ECHORD++

Publisher

Hindawi Limited

Subject

General Immunology and Microbiology,General Biochemistry, Genetics and Molecular Biology,General Medicine

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