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HOMe-IMprove Telerrehabilitation System

HOMe-IMprove Telerrehabilitation System for CHilDren With Cerebral Palsy

Status
Not yet recruiting
Phases
Unknown
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT07091461
Acronym
HOMIMTES-CHilD
Enrollment
24
Registered
2025-07-29
Start date
2026-03-01
Completion date
2027-04-01
Last updated
2026-02-05

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

Conditions

Cerebral Palsy Infantile

Keywords

home, children, infantile cerebral palsy, family, upper extremity, balance

Brief summary

This pilot study aims to assess the feasibility, adherence, and preliminary efficacy of a home-based telerehabilitation protocol using the HOME Kit Tablet system in children aged 6 to 18 years with cerebral palsy. The study follows a randomized controlled design with parallel groups and single-blind evaluation. The intervention group will use a digitally supervised rehabilitation system, while the control group will follow a traditional home therapy protocol without technological tools.

Interventions

DEVICEHOME Kit Tablet-based Telerehabilitation

Device-based behavioral intervention (motor, cognitive, and communication rehabilitation)

OTHERConventional Home Physiotherapy

Participants in this arm will follow a conventional home rehabilitation protocol, focusing on upper limb function and postural control. The protocol includes traditional exercises prescribed and explained by a physiotherapist. Follow-up will be conducted through weekly phone calls to reinforce adherence and resolve concerns.

Sponsors

University of Castilla-La Mancha
Lead SponsorOTHER

Study design

Allocation
RANDOMIZED
Intervention model
PARALLEL
Primary purpose
TREATMENT
Masking
SINGLE (Outcomes Assessor)

Eligibility

Sex/Gender
ALL
Age
6 Years to 18 Years
Healthy volunteers
No

Inclusion criteria

* Confirmed diagnosis of infantile unilateral cerebral palsy * Age between 6 and 18 years * Stable home Wi-Fi access and space to perform exercises * Manual Ability Classification System (MACS) level ≤ 3 * Informed consent from legal guardian and assent from the child (if \<12 years)

Exclusion criteria

* Severe neurological or psychiatric comorbidities * Recent orthopedic surgery (\<12 months) or botulinum toxin treatment (\<6 months) * Concurrent participation in other intervention studies

Design outcomes

Primary

MeasureTime frameDescription
Change in postural control assessed by stabilometric platformbaseline, immediately after the intervention, 1 month after interventionPostural control is evaluated using a stabilometric platform, which quantitatively measures center of pressure (CoP) displacement and sway area during quiet standing. The main outcome is the mean sway area in square centimeters (cm²), with lower values indicating better postural stability.
Change in balance performance assessed by the Pediatric Berg Balance Scale (PBS)baseline, immediately after the intervention, 1 month after interventionThe PBS is a 14-item observational tool designed to measure balance in children. Scores range from 0 to 56; higher scores indicate better balance function.
Change in unimanual hand function assessed by the Assisting Hand Assessment (AHA)baseline, immediately after the intervention, 1 month after interventionThe AHA measures how effectively children with unilateral cerebral palsy use their affected hand in bimanual tasks. Total scores range from 0 to 100; higher scores indicate better hand function.
Change in upper limb performance assessed by the Shriners Hospital for Children Upper Extremity Evaluation (SHUEE)baseline, immediately after the intervention, 1 month after interventionThe SHUEE evaluates spontaneous and dynamic use of the upper limb. Scores range from 0 to 100; higher scores indicate better function.
Change in manual ability assessed by the Children's Hand-use Experience Questionnaire (CHEQ)baseline, immediately after the intervention, 1 month after interventionThe CHEQ is a parent-reported measure that assesses the child's experience using their affected hand in daily tasks. Item scores and mean summary scores; higher scores reflect better experiences.
Change in gross manual dexterity assessed by the Box and Block Testbaseline, immediately after the intervention, 1 month after interventionThe Box and Block Test assesses gross manual dexterity by counting the number of blocks moved from one compartment to another in one minute. Higher numbers indicate better manual dexterity.

Secondary

MeasureTime frameDescription
Change in participation in daily activities assessed by the Participation and Environment Measure for Children and Youth (PEM-CY)baseline, immediately after the intervention, 1 month after interventionThe PEM-CY questionnaire evaluates participation frequency, involvement, and environmental supports and barriers across home, school, and community settings in children and youth. Scores are reported as frequency (number of activities per week), level of involvement (1-5 scale), and percentage of environmental barriers identified. Higher scores in frequency and involvement indicate greater participation, while higher percentages of environmental barriers reflect more challenges. Outcomes will be summarized for each domain (home, school, community) separately.
Change in individual goal achievement assessed by Goal Attainment Scaling (GAS)baseline, immediately after the interventionGoal Attainment Scaling (GAS) is a participant-centered outcome measure that evaluates the extent to which individualized rehabilitation goals are achieved. Each participant collaborates with the therapist to set specific goals at baseline, which are rated on a 5-point scale ranging from -2 (much less than expected outcome) to +2 (much more than expected outcome), with 0 representing the expected level of achievement. Higher total GAS scores reflect greater goal attainment and better functional improvement.
Change in occupational performance and satisfaction assessed by the Canadian Occupational Performance Measure (COPM)baseline, immediately after the intervention, 1 month after interventionThe COPM measures self-perceived performance and satisfaction in daily activities identified as important by the participant or caregiver. Participants rate their performance and satisfaction on a 10-point scale (1-10), with higher scores indicating better performance and greater satisfaction. The primary outcomes are changes in COPM performance and satisfaction scores between baseline and post-intervention assessments.
Change in user satisfaction evaluated with a 5-point Likert-scale questionnaireimmediately after the intervention.User satisfaction with the intervention will be assessed using a structured questionnaire based on a 5-point Likert scale, ranging from 1 (very dissatisfied) to 5 (very satisfied). The total score will be calculated as the mean of individual item responses. Higher scores indicate greater satisfaction with the rehabilitation protocol and the HOME Kit system. The questionnaire includes items related to usability, comfort, perceived usefulness, and motivation.

Contacts

CONTACTRocío Palomo-Carrión, PT PhD
Rocio.Palomo@uclm.es34926051821

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 6, 2026