ROBot Assisted Physical Training of Older Patients During acUte hospitaliSaTion

Physical Inactivity Clinical Trial

— ROBUST  

Official title:

ROBot Assisted Physical Training of Older Patients During acUte hospitaliSaTion (ROBUST) - a Randomised Controlled Trial

Clinical Trial Details — Status: Recruiting

Administrative data

• NCT number: NCT05782855
• Other study ID #: ROBUST
• Status: Recruiting
• Phase: N/A
• Start date: January 5, 2023
• Est. completion date: July 31, 2025

Study information

• Verified date: December 2023
• Source: Odense University Hospital
• Contact: Ann Sophia Bertelsen, PhD student
• Phone: +4529631326
• Email: ann.sophia.bertelsen[@]rsyd.dk
• Is FDA regulated: No
• Study type: Interventional

Clinical Trial Summary

This study aims to address if robot assisted physical training can prevent functional decline during acute hospitalisation in older geriatric patients.

Design: blinded RCT. Patients: n = 488. Primary outcome is functional decline, assessed by Barthel-Index and 30s chair stand test. One- and three months follow-up.

Description:

Introduction:

Inactivity during hospitalisation is associated with significant risk of functional decline especially in older patients. This have major impact on the individual level due to decreased wellbeing and higher level of dependency and on the society level due to increased caregiver burden following hospital discharge. This study aims to address if robot assisted physical training can prevent functional decline during acute hospitalisation in older geriatric patients.

Methods:

ROBUST is a blinded RCT. Patients (n = 488) admitted with acute medical illness to Department of Geriatric Medicine, Odense University Hospital will be randomised to usual care and robot assisted active strength training of lower extremities twice daily (intervention group) or usual care and robot assisted passive sham training (control group) until discharge. Both groups will receive protein supplements.

Inclusion criteria: ≥65 years of age, able to ambulate before hospitalisation, expected length of stay ≥2 days.

Exclusion criteria: Able to ambulate without assistance during current hospitalisation, severe dementia, delirium, conditions contradicting robot training.

The primary outcome, functional decline, will be assessed by Barthel-Index and 30s chair stand test.

Secondary outcomes include Quality of life (EQ-5D), Geriatric Depression Scale, Fear of falling (FES-I), cognition (MMSE), qualitative interviews, falls, caregiver burden, discharge destination, readmissions, healthcare costs, sarcopenia, and mortality.

Outcomes will be assessed at admission, discharge, and one- and three months follow-up. Data on comorbidity, medications, blood samples, and clinical frailty scale will be collected.

Discussion: This study will investigate the effects of in-hospital robot assisted strength training on functional status in older patients with multimorbidity.

Recruitment information / eligibility

• Status: Recruiting
• Enrollment: 488
• Est. completion date: July 31, 2025
• Est. primary completion date: July 31, 2024
• Accepts healthy volunteers: No
• Gender: All
• Age group: 65 Years and older

Eligibility

Inclusion Criteria:

• =65 years of age

• Able to ambulate before hospitalisation (with/without assistance)

• Able to communicate with the research team

• Expected length of stay =2 days

• Residing on Funen, Denmark

Exclusion Criteria:

• Able to ambulate without assistance during current hospitalisation

• Known severe dementia

• Positive Confusion and Assessment Method score (20)

• Patients who have received less than 3 training sessions at discharge

• Terminal illness

• Recent major surgery or lower extremity bone fracture in the last 3 months

• Conditions contradicting use of ROBERT (unstable vertebral-, pelvic, or lower extremity fractures; high intracranial pressure; pressure ulcers or risk of developing pressure ulcers due to fragile skin; patients with medical instability)

• Metastases at femur or hip

• Deemed not suitable for mobilization sessions with the robot by the healthcare professional

• If the patient weighs more than 165 kg (the robot cannot lift the leg if the patient is severely overweight)

Related Conditions & MeSH terms

• Acute Illness
• Functional Decline
• Physical Inactivity

Intervention

Other:
• Active Robot assisted physical training during acute hospitalisation
Active training is delivered by an innovative training robot (ROBERT®). The robot is handled by staff who attaches the robot to the patient's leg. The staff programs the exercise movement, whereby the robot remembers the movement. The robot holds the patient's leg and perform extension of hip and knee. The patient must use their muscular power to stretch the leg while ROBERT® provides resistance. Training is defined as a minimum of three sessions before discharge.
• Passive Robot assisted physical training during acute hospitalisation
Passive training is delivered by an innovative training robot (ROBERT®). The robot is handled by staff who attaches the robot to the patient's leg. The staff programs the movement, whereby the robot remembers the movement. The robot holds the patient's leg and perform passive extension of hip and knee. ROBERT® moves the leg independently without the patient using any muscle power. Training is defined as a minimum of three sessions before discharge.

Locations

Country	Name	City	State
Denmark	Odense University Hospital/Svendborg Hospital	Svendborg

Sponsors (1)

Lead Sponsor	Collaborator
Odense University Hospital

Country where clinical trial is conducted

Denmark, 

References & Publications (1)

Bertelsen AS, Storm A, Minet L, Ryg J. Use of robot technology in passive mobilization of acute hospitalized geriatric medicine patients: a pilot test and feasibility study. Pilot Feasibility Stud. 2020 Jan 6;6:1. doi: 10.1186/s40814-019-0545-z. eCollection 2020. — View Citation

Outcome

Type	Measure	Description	Time frame	Safety issue
Primary	Change from baseline Barthel Index 100	Functional evaluation assessed by Barthel Index 100. The Barthel Index is an ordinal scale used to measure performance in activities of daily living (ADL). Ten variables describing ADL and mobility are scored, a higher number being a reflection of greater ability to function independently following hospital discharge.	Change from baseline (day of hospital admission) to day of hospital discharge (an average of 1 week)
Primary	Change from baseline 30 Second Sit to Stand Test	Functional evaluation assessed by 30 Second Sit to Stand Test . The 30 Second Sit to Stand Test is for testing leg strength and endurance in older adults.	Change from baseline (day of hospital admission) to day of hospital discharge (an average of 1 week)
Secondary	Quality of life EQ-5D	Quality of life is assessed using the questionaire Quality of life EuroQol-5 dimension (EQ-5D). The EQ-5D comprises five dimensions (mobility, self-care, usual activities, pain/discomfort and anxiety/depression) each with three levels (no problems, some problems, extreme problems/unable), thus generating 243 possible health states.; The EQ-5D questionnaire also includes a Visual Analog Scale (VAS), by which respondents can report their perceived health status with a grade ranging from 0 (the worst possible health status) to 100 (the best possible health status).	Day of hospital admission; day of hospital discharge (an average of 1 week); 1 month follow-up; 3 months follow-up.
Secondary	Mood status	Mood status are assessed by the 15-item Geriatric Depression Scale. The Short Form GDS consisting of 15 questions. Of the 15 items, 10 indicated the presence of depression when answered positively, while the rest indicated depression when answered negatively. Scores of 0-4 are considered normal, depending on age, education, and complaints; 5-8 indicate mild depression; 9-11 indicate moderate depression; and 12-15 indicate severe depression.	Day of hospital admission; day of hospital discharge (an average of 1 week); 1 month follow-up; 3 months follow-up.
Secondary	Concern about falling including number of falls	Concern about falling is assessed using the 16-item Short Falls Efficacy Scale International (Short FES-I) questionaire. To calculate the Short FES-I score when all items are completed, simply add the scores for each item together to give a total that ranges as follows: minimum 7 (no concern about falling) to maximum 28 (severe concern about falling).	Day of hospital admission; day of hospital discharge (an average of 1 week); 1 month follow-up; 3 months follow-up.
Secondary	Patient perspective by qualitative interviews	Qualitative semi-structured in-depth interviews will be performed with at least 12 patients at discharge and 1 month follow-up to explore their perspectives and experiences (PRO/PRE). The qualitative interviews will provide further and deeper explanations of the results from the quantitative parts of the study. By using this mixed-methods approach the research results will be strengthen by the complementary findings. The analysis of the qualitative data will be completed in line with manifest content analysis by Graneheim and Lundman. Data will be handled using the software NVivo	Day of hospital discharge (an average of 1 week); 1 month follow-up.
Secondary	Cognitive function	Cognitive function is assessed by the Mini Mental State Examination. The Mini-Mental State Examination (MMSE) is a set of 11 questions that is used to check for cognitive impairment (problems with thinking, communication, understanding and memory). The maximum score for the MMSE is 30. A score of 25 or higher is classed as normal. If the score is below 24, the result is usually considered to be abnormal, indicating possible cognitive impairment.	Day of hospital admission; day of hospital discharge (an average of 1 week); 1 month follow-up; 3 months follow-up.
Secondary	Muscle quantity	Muscle quantity is assessed using bioelectrical impedance by InBodyS10. Bioelectrical impedance analysis (BIA) is a method for estimating body composition, in particular body fat and muscle mass.	Day of hospital admission; day of hospital discharge (an average of 1 week); 1 month follow-up; 3 months follow-up.
Secondary	Sarcopenia	Sarcopenia is assessed based on the 2019 European guidelines by Cruz-Jentoft AJ, Bahat G, Bauer J, Boirie Y, Bruyère O, Cederholm T, et al.	Day of hospital admission; day of hospital discharge (an average of 1 week); 1 month follow-up; 3 months follow-up.
Secondary	Need of care at home	Individual level data from the municipalities will be used to assess amount of need of care/home care provided by the municipality 3 months before admission and 3 months after discharge. Need of care at home is devided in the following categories: practical help, personnel care, nursing and training. Amount of need of care will be presented in hours.	From 3 months prior to day of hospital admission to 3 months following day of hospital discharge.
Secondary	Length of hospital stay	Length of hospital stay will be defined as number of days in geriatric department.	From day of hospital admission to day of hospital discharge (an average of 1 week).
Secondary	Discharge destination	Data about discharge destination will be collected at the day of discharge (own home, temporary rehabilitation units, nursing homes)	Day of hospital discharge (an average of 1 week).
Secondary	Rate of hospital readmission	Patients will be followed through a review of medical records for any unplanned hospitalisation within 1 month after discharge.; Readmission definition: any unplanned hospital contact with a duration of 12+hours, occurring between 4 hours and 30 days after discharge from the Department of Geriatric Medicine.	30 days following day of hospital discharge.
Secondary	Health care cost evaluation	A researcher in health care economics will perform a health care cost evaluation addressing running cost using ROBERT, discharge destination, hospital readmissions, care giver burden, and visits to the general practitioner after 3 months.	3 months follow-up.
Secondary	Mortality	Administrative registers will be used to assess mortality at 1- and 3- months follow-up.	1- and 3-months follow-up.
Secondary	Change from baseline Barthel Index 100	Functional evaluation assessed by Barthel Index 100. The Barthel Index is an ordinal scale used to measure performance in activities of daily living (ADL). Ten variables describing ADL and mobility are scored, a higher number being a reflection of greater ability to function independently following hospital discharge.	Change from baseline (day of hospital admission) to 1 month follow-up and 3 months follow-up.
Secondary	Change from baseline 30 Second Sit to Stand Test	Functional evaluation assessed by 30 Second Sit to Stand Test . The 30 Second Sit to Stand Test is for testing leg strength and endurance in older adults.	Change from baseline (day of hospital admission) to 1 month follow-up and 3 months follow-up.
Secondary	Clinical Frailty Scale	The 9-point Clinical Frailty Scale (CFS) with pictograms is used at baseline before randomisation, at discharge, and at 1- and 3-month follow-up (28) to examine the impact of the exercise intervention on frailty and to determine the impact of baseline frailty on the effectiveness of the intervention	Change from baseline (day of hospital admission) to 1 month follow-up and 3 months follow-up.