Effectiveness of virtual reality devices in the rehabilitation of adults with stroke

TECHNOREHAB: randomized clinical trial for the technological rehabilitation of adults with stroke

Status

Active, not recruiting

Phases

Unknown

Study type

Interventional

Source

ISRCTN

Registry ID

ISRCTN27760662

Enrollment

Registered

2020-06-16

Start date

2018-04-17

Completion date

Unknown

Last updated

2023-04-17

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Motor injuries and functional dependence in adults with stroke Circulatory System Cerebral infarction

Interventions

Rehabilitation programs using virtual reality. The use of games specifically designed for the rehabilitation process. Virtual reality devices: HandTutor, 3DTutor and Rehametrics. The assignment to e

20 min. of HandTutor training

5 min. of Rehametrics placement (bobath ball, chair, weights, etc.) and 20 min. of Rehametrics training. The selected exercises are repeated every day. Every day the difficulty increases (number of o

Eligibility

Sex/Gender

All

Inclusion criteria

Inclusion criteria: 1. Age between 18 and 85 years old 2. Diagnosed stroke 3. Difficulties motor skills of the upper limb 4. Dependence in daily life activities 5. Time of evolution since diagnosis: maximum 6 months 6. No other disabling pathology prior to the injury 7. Not having a life expectancy of less than 6 months 8. Acceptance and signature of the informed consent

Exclusion criteria

Exclusion criteria: 1. Presence of other neurological disorders 2. Severe heminegligency 3. Psychiatric disorders that hinder participation 4. Signature of revocation of consent

Design outcomes

Primary

Measure	Time frame
1. The impact of stroke on daily life is measured using SIS 3.0 scale at baseline, the end of study (15 sessions), 3 and 6 months 2. Walking capacity and balance is measured using Tinetti Test at baseline, the end of study (15 sessions), 3 and 6 months 3. The motor function of the upper limb is measured using Ara-T and Fugl-Meyer at baseline, the end of study (15 sessions), 3 and 6 months 4. Perceived quality of life is measured using EuroQool-5L Test at baseline, the end of study (15 sessions), 3 and 6 months	—

Measure

Time frame

1. The impact of stroke on daily life is measured using SIS 3.0 scale at baseline, the end of study (15 sessions), 3 and 6 months 2. Walking capacity and balance is measured using Tinetti Test at baseline, the end of study (15 sessions), 3 and 6 months 3. The motor function of the upper limb is measured using Ara-T and Fugl-Meyer at baseline, the end of study (15 sessions), 3 and 6 months 4. Perceived quality of life is measured using EuroQool-5L Test at baseline, the end of study (15 sessions), 3 and 6 months

—

Secondary

Measure	Time frame
1. Resistance to movement in the paretic upper limb is measured by the Modified Ashworth Scale at baseline, the end of study (15 sessions), 3 and 6 months 2. User satisfaction with the device is measured with the Quebec Scale at the end of study (15 sessions)	—

Countries

Spain

Outcome results

None listed

Source: ISRCTN (via WHO ICTRP) · Data processed: Feb 11, 2026