Use of virtual reality based therapy in the elderly

ISRCTN ISRCTN11923623
DOI https://doi.org/10.1186/ISRCTN11923623
EudraCT/CTIS number 2019-004392-40
Submission date
11/11/2019
Registration date
18/12/2019
Last edited
23/06/2022
Recruitment status
No longer recruiting
Overall study status
Completed
Condition category
Signs and Symptoms
Prospectively registered
Protocol
Statistical analysis plan
Results
Individual participant data

Plain English summary of protocol

Background and study aims
Impaired functional mobility of elders is frequently associated with loss of independence. Maintaining functional independence must be a priority in elderly care plans. Achieving autonomous participation in their own real everyday environment would contribute to improving their community involvement and also their overall health. The rehabilitation programs that include the practice of real activities are more effective. The use of virtual reality game technology (VRGT) has the potential to offer treatment settings very similar to actual environments and tasks. Interactive simulations allow elders to practice repetitive motor exercises directly connected with the movements needed in activities of daily living. The aim of this study is to evaluate the effectiveness of virtual reality systems for rehabilitation and improvement of quality of life of the elderly.

Who can participate?
Frail and pre-frail adults aged 60 or over

What does the study involve?
Participants are randomly allocated to one of two groups. The experimental group receives 24 individual training sessions with Virtual Reality systems (45 minutes, twice a week), provided by an occupational therapist. Twelve exergames (Nintendo and Xbox) were selected according to their cognitive and motor demands. The sequence of the games was pre-determined at the start of the study. Each game is repeated twice in each session and scores are recorded for each attempt. The first attempt is with the assistance of an occupational therapist to correct the movements and posture of participants using manual guidance and verbal feedback, while the subsequent attempt is performed independently but under the supervision of the occupational therapist. The duration of each game is about 4-5 minutes. The time required to change one game to another is about three minutes, during which time participants sit on a chair to rest. The control group is not treated with virtual reality systems. They only perform their daily activities.

What are the possible benefits and risks of participating?
The possible benefits of using virtual reality technology in rehabilitation processes with elderly people include improvement of balance and walking ability, improvement of cognitive status and improvement in the performance of daily life activities.
The possible adverse effects include fatigue, muscle pain and headaches.

Where is the study run from?
The study has been designed from the University of Castilla La Mancha (Spain) and rehabilitation sessions with technology based on virtual reality are being developed in two nursing homes: Nursing Home “El Lucero” (Talavera de la Reina, Spain) and Nursing Home “Benquerencia” (Toledo, Spain).

When is the study starting and how long is it expected to run for?
January 2019to January 2020

Who is funding the study?
Investigator initiated and funded

Who is the main contact?
1. Ana Isabel Corregidor Sánchez
anaisabel.corregidor@uclm.es
2. Dr Begoña Polonio López
begona.polonio@uclm.es

Contact information

Mrs Ana Isabel Corregidor Sánchez
Scientific

Avenida Real Fábrica de Sedas sin número
Talavera de la Reina
45600
Spain

ORCiD logoORCID ID 0000-0001-8768-1942
Phone +34 (0)630793081
Email anaisabel.corregidor@uclm.es
Dr Begoña Polonio-López
Scientific

Faculty of Health Sciences
University of Castilla-La Mancha
Av. Real Fábrica de Sedas s/n
Talavera de la Reina
45600
Spain

ORCiD logoORCID ID 0000-0003-2922-7519
Phone +34 (0)682247830
Email Begona.Polonio@uclm.es

Study information

Study designLongitudinal multicenter prospective and analytical study of random assignment with experimental group and control group
Primary study designInterventional
Secondary study designRandomised parallel trial
Study setting(s)Other
Study typeTreatment
Participant information sheet Not available in web format, please use conact details to request a participant information sheet
Scientific titleEffectiveness of virtual reality based therapy in the rehabilitation of the elderly
Study acronymVR Elderly
Study objectives1. The use of virtual reality devices improves the balance and wandering of older people.
2. The use of virtual reality games improves the cognitive situation of older people
3. Participation in a virtual reality exercise program produces changes sensation of well-being and quality of life
Ethics approval(s)Approved 23/09/2014, Clinical Research Ethical Committee of the Talavera de la Reina Integrated Management Area (CEIC del AGI de Talavera de la Reina, Hospital Nuestra Señora del Prado. Ctra. Nacional V, km. 114 . 45600, Talavera de la Reina (Toledo); Tel: +34 (0)925 80 36 OO Ext. 86.316; Email: varroyo@sescam.org), ref: 5/2018
Health condition(s) or problem(s) studiedFunctional impairment and frailty in the elderly
InterventionRehabilitation programs using Virtual Reality. The use of commercial game consoles and exergames, as well as games specifically designed for the rehabilitation process were both admitted.

The assignment to each of the groups was parallel. Participants were randomly assigned to the experimental group (EG) or control group (CG), with an allocation ratio of 1:1. Blinding of trial participants and the intervention facilitator was not possible.

Experimental group:
Participants received 24 individual training sessions with Virtual Reality systems (45 min, twice a week), provided by an occupational therapist. Twelve exergames (Nintendo and Xbox) were selected according to their cognitive and motor demands. The sequence of the games was pre-determined at baseline of the study. Each game was repeated twice in each session and scores were recorded for each attempt. The first attempt was with the assistance of an occupational therapist to correct the movements and posture of participants using manual guidance and verbal feedback, while the subsequent attempt was performed independently but under supervision of the occupational therapist. The duration of each game was approximately 4-5 min. The time required to change one game to another was approximately three minutes, during which time participants sat on a chair to rest.

Control group:
The control group was not treated with virtual reality systems. They only performed their daily activities.
Intervention typeBehavioural
Primary outcome measure1. Functional performance (capacity to perform the activities of daily living) is measured using AMPS scale (Assessment Motor and Process Skill) and Barthel Index at baseline and the end of study (3 months)
2. Walking capacity and balance is measured using Tinetti Test and Test Up and Go (TUG) at baseline and the end of study (3 months)
3. Physical capacity is measured using the Senior Fitness Test (SFT) at baseline and the end of study (3 months)
4. Perceived quality of life is measured using the Filadelfia Test (SFT) at baseline and the end of study (3 months)
5. Cognition capacity is measured using Mini Mental State Examination (MMSE) at baseline and the end of study (3 months)
Secondary outcome measuresOpinion on the use of technology is measured using Subjective Scale Use of Virtual Reality, a questionnaire developed for this study, at 3 months after the participants have completed 24 treatments
Overall study start date02/01/2019
Completion date02/01/2020

Eligibility

Participant type(s)Patient
Age groupSenior
SexBoth
Target number of participants20 participants in each group
Total final enrolment40
Key inclusion criteriaPersons over age 60 without neurological, osteoarticular, or other type of disease that severely affects functional independence
Key exclusion criteriaNeurological and osteoarticular conditions that severely affect functional independence
Date of first enrolment02/05/2019
Date of final enrolment02/09/2019

Locations

Countries of recruitment

  • Spain

Study participating centre

Ana Isabel Corregidor Sánchez. Universidad de Castilla la Mancha: Facultad Ciencias de la Salud
Avenida Real Fábrica de Sedas s/n
Talavera De Lareina
45600
Spain

Sponsor information

Facultad Ciencias de la Salud. Universidad de Castilla la Mancha
University/education

Avenida Real Fábrica de Sedas sin número
Talavera de la Reina
45600
Spain

Phone +34 (0)630793081
Email anaisabel.corregidor@uclm.es
Website www.uclm.es
ROR logo "ROR" https://ror.org/05r78ng12

Funders

Funder type

Other

Investigator initiated and funded

No information available

Results and Publications

Intention to publish date01/03/2020
Individual participant data (IPD) Intention to shareYes
IPD sharing plan summaryAvailable on request
Publication and dissemination planPlanned publication in a high-impact peer-reviewed journal.
IPD sharing planThe datasets generated during and/or analysed during the current study are/will be available upon request from Ana Isabel Corregidor Sánchez (Anaisabel.corregidor@uclm.es) .

Study outputs

Output type Details Date created Date added Peer reviewed? Patient-facing?
Basic results 18/02/2021 18/02/2021 No No

Additional files

ISRCTN11923623_BasicResults_18Feb2021.pdf
uploaded 18/02/2021

Editorial Notes

23/06/2022: Final total enrollment updated.
10/06/2022: Contact details updated.
18/02/2021: The basic results of this trial have been uploaded as an additional file.
13/11/2019: Trial's existence confirmed by ethics committee.