Skip to content

Effects of Social Robot-Based interventions in improving cognition, communication and social skills of children with Motor Movement Disorders (MMD)

Randomized controlled trial to evaluate the effect of Social Robot-Based interventions using QTRobot on cognition, communication, and social skills in children aged 5–12 years with cerebral palsy.

Status
Recruiting
Phases
Unknown
Study type
Interventional
Source
ANZCTR
Registry ID
ACTRN12625001214426
Enrollment
42
Registered
2025-11-04
Start date
2025-09-02
Completion date
2026-06-29
Last updated
2025-11-10

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

Conditions

None listed

Brief summary

This study aims to find out whether interacting with QTRobot can help improve thinking, communication, and social skills in children aged 5 to 12 with cerebral palsy. We believe that regular sessions with the robot-based interventions will support children’s development in these areas. The children will take part in individual sessions every other day a week for six to eight weeks at a rehabilitation center.

Interventions

Scripts and behavioural mapping: The robot uses pre-programmed scripts involving speech, emotional expressions (e.g. happy, sad, surprised), gestures (e.g. waving, nodding), and turn-taking prompts to facilitate child–robot interaction. Games and tasks: Sessions include storytelling, object naming, emotion recognition, imitation of simple arm and leg movements, role-play dialogues, memory games, and turn-taking social tasks. Adherence monitoring: Attendance at each session will be recorded. Th

Scripts and behavioural mapping: The robot uses pre-programmed scripts involving speech, emotional expressions (e.g. happy, sad, surprised), gestures (e.g. waving, nodding), and turn-taking prompts to facilitate child–robot interaction. Games and tasks: Sessions include storytelling, object naming, emotion recognition, imitation of simple arm and leg movements, role-play dialogues, memory games, and turn-taking social tasks. Adherence monitoring: Attendance at each session will be recorded. The therapist will complete session checklists. Sessions will be video-recorded for fidelity checks. Where applicable, QTRobot usage metrics will be stored. Parental feedback will also be collected on engagement and participation. Frequency and duration: Each child will complete 10 sessions, 7-10 minutes each, delivered thrice per week over 4 weeks. Individualisation: Tasks will be adapted according to the child’s age, motor and cognitive level, and communication ability. Adjustments will be made by the therapist using QTRobot software (e.g. simpler vocabulary, shorter sentences, reduced motor complexity, or increased social challenge). Adaptations are made at the start of the program and updated as needed during sessions based on progress and therapist observation. Crossover and washout period: As this is a crossover trial, participants will first complete the QTRobot intervention, then after a washout period of 3 months, they will switch to the comparator/control condition (or vice versa, depending on randomisation). This period is intended to minimise carryover effects.

Sponsors

Ministry of Higher Education and Science
Lead SponsorGovernment body

Study design

Allocation
Randomised controlled trial
Intervention model
Crossover
Primary purpose
Treatment
Masking
Open (masking not used)

Eligibility

Sex/Gender
All
Age
5 Years to 12 Years
Healthy volunteers
No

Inclusion criteria

Children aged between 5 and 12 years. Diagnosis of spastic cerebral palsy (including hemiplegic, diplegic, and quadriplegic types). Ability to understand and follow simple verbal instructions. Stable medical condition, with no recent changes in medication or therapy. Ability to attend sessions at the rehabilitation center regularly. Parental or guardian consent and assent from children obtained. Cognitive and physical ability sufficient to interact with the robot.

Exclusion criteria

Severe cognitive impairments that prevent understanding simple instructions. Comorbid serious neurological disorders (e.g., epilepsy with frequent seizures). Severe visual or hearing impairments that interfere with interaction with the robot. Inability to attend sessions at the rehabilitation center (e.g., due to medical or logistical reasons). Presence of other medical conditions that may affect the safety or outcomes of the study.

Outcome results

None listed

Source: ANZCTR · Data processed: Feb 4, 2026