TY - JOUR

T1 - Robotic technology (ROBERT®) to enhance muscle strength in the hip flexor muscles following spinal cord injury

T2 - a feasibility study

AU - Sørensen, S L

AU - Poulsen, I

AU - Harvey, L A

AU - Biering-Sørensen, F

AU - Nielsen, J F

N1 - © 2024. The Author(s).

PY - 2024

Y1 - 2024

N2 - STUDY DESIGN: Feasibility study.OBJECTIVE: To determine the feasibility of conducting a large trial designed to determine whether the ROBERT® can be used to increase the strength of the hip flexor muscles after spinal cord injury (SCI). The ROBERT® is a robotic device that provides assisted active movement while supporting the weight of the leg. Focus was on recruitment capability, suitability, and acceptability of the intervention and outcome measure.SETTING: Specialised SCI centre in Denmark.METHODS: All first-time admitted patients were screened to assess participant recruitment capability. Four people with SCI < 3 months tested a protocol consisting of 60 repetitions of hip flexion in supine conducted with the assistance of the ROBERT® three times a week for 4 weeks. Feasibility was assessed based on adherence to the protocol and completion rate and from the participants' perspectives. Maximal voluntary contraction (MVC) was accessed at baseline and four weeks.RESULTS: The recruitment rate was 8% (7 months). The four participants completed 44 out of 48 sessions (92%). No adverse events occurred. One physiotherapist was required to set-up and supervise each session. The active exercise time varied from 7.5 to 17 min. The participants found the ROBERT® a good supplement to their usual rehabilitation. We were able to measure MVC in even very weak hip flexor muscles with a dynamometer MicroFET2 fixed to a frame.CONCLUSION: The ROBERT® was feasible and acceptable. The participants perceived it as a supplement, not a replacement to usual physiotherapy. However, recruitment to the study was slow.TRIAL REGISTRATION: ClinicalTrials.gov NCT05558254. Registered 28th September 2022.

AB - STUDY DESIGN: Feasibility study.OBJECTIVE: To determine the feasibility of conducting a large trial designed to determine whether the ROBERT® can be used to increase the strength of the hip flexor muscles after spinal cord injury (SCI). The ROBERT® is a robotic device that provides assisted active movement while supporting the weight of the leg. Focus was on recruitment capability, suitability, and acceptability of the intervention and outcome measure.SETTING: Specialised SCI centre in Denmark.METHODS: All first-time admitted patients were screened to assess participant recruitment capability. Four people with SCI < 3 months tested a protocol consisting of 60 repetitions of hip flexion in supine conducted with the assistance of the ROBERT® three times a week for 4 weeks. Feasibility was assessed based on adherence to the protocol and completion rate and from the participants' perspectives. Maximal voluntary contraction (MVC) was accessed at baseline and four weeks.RESULTS: The recruitment rate was 8% (7 months). The four participants completed 44 out of 48 sessions (92%). No adverse events occurred. One physiotherapist was required to set-up and supervise each session. The active exercise time varied from 7.5 to 17 min. The participants found the ROBERT® a good supplement to their usual rehabilitation. We were able to measure MVC in even very weak hip flexor muscles with a dynamometer MicroFET2 fixed to a frame.CONCLUSION: The ROBERT® was feasible and acceptable. The participants perceived it as a supplement, not a replacement to usual physiotherapy. However, recruitment to the study was slow.TRIAL REGISTRATION: ClinicalTrials.gov NCT05558254. Registered 28th September 2022.

KW - Humans

KW - Feasibility Studies

KW - Robotic Surgical Procedures

KW - Spinal Cord Injuries/rehabilitation

KW - Muscle Strength

KW - Muscles

U2 - 10.1038/s41394-024-00630-9

DO - 10.1038/s41394-024-00630-9

M3 - Journal article

C2 - 38600074

VL - 10

JO - Spinal cord series and cases

JF - Spinal cord series and cases

SN - 2058-6124

IS - 1

M1 - 20

ER -