NCT07797439

Brief Summary

The goal of this clinical study is to learn whether Neuromotor Task Training (NTT) may help improve functional motor skills in autistic children who have motor difficulties. The main question it aims to answer is: Does Neuromotor Task Training help autistic children improve a motor skill that is difficult for them in daily life? This study will include autistic children with motor difficulties. Each child will work on one functional motor skill chosen according to their needs and daily-life goals. Examples may include skills such as catching a ball, jumping rope, putting on a coat, or another meaningful motor task. Participants will take part in an initial assessment of their motor abilities. They will then choose, with their family and the researcher, a functional motor skill to work on. The selected skill will be assessed repeatedly before, during, and after the training period. Participants will receive Neuromotor Task Training sessions focused on this skill. They will also be followed after the training period to see whether the motor skill is maintained. Neuromotor Task Training is a task-oriented rehabilitation approach. It focuses on practicing meaningful motor skills in conditions that are progressively adapted to the child. The task, the environment, and the feedback provided by the therapist may be adjusted during the sessions to support motor learning. This study uses a single-case experimental design. This means that each participant's progress is measured repeatedly over time. The researchers will examine whether motor performance changes after the start of the training and whether these changes are maintained after the training period.

Trial Health

63
Monitor

Trial Health Score

Automated assessment based on enrollment pace, timeline, and geographic reach

Enrollment
12

participants targeted

Target at below P25 for not_applicable

Timeline
14mo left

Started Oct 2026

Geographic Reach
1 country

1 active site

Status
not yet recruiting

Health score is calculated from publicly available data and should be used for screening purposes only.

Trial Relationships

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Study Timeline

Key milestones and dates

Study Progress1%
Oct 2026Dec 2027

First Submitted

Initial submission to the registry

August 24, 2026

Completed
8 days until next milestone

First Posted

Study publicly available on registry

September 1, 2026

Completed
1 month until next milestone

Study Start

First participant enrolled

October 1, 2026

Completed
8 months until next milestone

Primary Completion

Last participant's last visit for primary outcome

June 1, 2027

Expected
6 months until next milestone

Study Completion

Last participant's last visit for all outcomes

December 1, 2027

Last Updated

September 25, 2026

Status Verified

September 1, 2026

Enrollment Period

8 months

First QC Date

August 24, 2026

Last Update Submit

September 22, 2026

Conditions

Keywords

Developmental Coordination DisorderMotor SkillsMotor DifficultiesMotor LearningMotor RehabilitationNeuromotor Task TrainingSingle-Case Experimental DesignTask-Oriented Training

Outcome Measures

Primary Outcomes (1)

  • Performance on the Individualized Functional Motor Skill

    Motor performance will be assessed using one predefined, task-specific, directly observable quantitative indicator for each individualized functional motor skill. Depending on the selected skill, the indicator may be the number or proportion of successful trials, completion time, accuracy, or another objective task-specific measure. The indicator and the direction indicating improvement will be defined before baseline and will remain unchanged throughout baseline, intervention, and follow-up. Each skill and participant will be analyzed separately in the original unit of measurement; data from different task-specific indicators will not be aggregated.

    Once weekly during the 6- to 9-week baseline phase, at each of the 10 intervention sessions, and once weekly during the 5-week post-intervention follow-up phase.

Secondary Outcomes (1)

  • Goal Attainment Scaling Attainment Level

    At baseline goal setting, after completion of the 10-session intervention, and at the end of the 5-week follow-up phase.

Study Arms (1)

Neuromotor Task Training

EXPERIMENTAL

Participants will be enrolled in three successive cohorts of four children. All participants will receive Neuromotor Task Training focused on an individualized functional motor skill. The cohort structure is used to support replication within the single-case experimental design. It does not correspond to different intervention groups.

Behavioral: Neuromotor Task Training

Interventions

Neuromotor Task Training is a task-oriented rehabilitation approach focused on the practice of meaningful functional motor skills. The therapist analyzes the selected task and adapts task constraints, environmental conditions, practice organization, and feedback to support motor learning. In this study, each participant will receive Neuromotor Task Training sessions targeting an individualized motor skill selected before the intervention phase.

Neuromotor Task Training

Eligibility Criteria

Age6 Years - 10 Years
Sexall
Healthy VolunteersNo
Age GroupsChild (0-17)

You may qualify if:

  • Children aged 6 to 10 years.
  • Diagnosis of autism spectrum disorder.
  • Presence of motor difficulties documented by clinical assessment and/or standardized motor assessment.
  • Ability to understand and participate in the proposed motor training sessions.
  • Written informed consent from the child's legal representative(s).
  • Child assent whenever possible, according to age and level of understanding.
  • Participation in the usual care pathway at the investigating center.

You may not qualify if:

  • Intelligence quotient below 70, when documented, or severe cognitive impairment preventing understanding of the tasks or participation in the training sessions.
  • Medical, neurological, orthopedic, or sensory condition that would contraindicate participation in motor training.
  • Uncontrolled epilepsy or any unstable medical condition that could interfere with participation.
  • Severe behavioral difficulties making repeated assessment or motor training impossible.
  • Ongoing participation in another interventional study that could interfere with the outcomes of this study.

Contact the study team to confirm eligibility.

Sponsors & Collaborators

Study Sites (1)

Groupe Hospitalier Nord-Essonne

Bures-sur-Yvette, Essone, 91440, France

Location

MeSH Terms

Conditions

Autism Spectrum DisorderMotor Skills Disorders

Condition Hierarchy (Ancestors)

Child Development Disorders, PervasiveNeurodevelopmental DisordersMental Disorders

Study Officials

  • Aurélien D'Ignazio, MSc

    Groupe Hospitalier Nord-Essonne

    PRINCIPAL INVESTIGATOR

Central Study Contacts

Aurélien D'Ignazio, MSc (PhD studend)

CONTACT

Study Design

Study Type
interventional
Phase
not applicable
Allocation
NA
Masking
NONE
Masking Details
This is an open-label, single-arm study. When feasible, video-recorded motor performances will be rated by an external outcomes assessor who is not involved in the intervention sessions and is masked to the study phase and timing of the assessment.
Purpose
TREATMENT
Intervention Model
SINGLE GROUP
Model Details: Single-case experimental design using a concurrent multiple-baseline design replicated across three successive cohorts of four participants. Within each cohort, introduction of Neuromotor Task Training will be staggered across participants, with baseline phases lasting approximately 6, 7, 8, and 9 weeks. All participants will receive the intervention targeting an individualized functional motor skill. Each participant will serve as their own control through repeated measurements collected during baseline, intervention, and follow-up phases.
Sponsor Type
OTHER
Responsible Party
SPONSOR

Study Record Dates

First Submitted

August 24, 2026

First Posted

September 1, 2026

Study Start

October 1, 2026

Primary Completion (Estimated)

June 1, 2027

Study Completion (Estimated)

December 1, 2027

Last Updated

September 25, 2026

Record last verified: 2026-09

Data Sharing

IPD Sharing
Will not share

Individual participant data will not be shared because the study includes a small sample of children and may involve sensitive clinical and video-recorded data. Sharing individual-level data could increase the risk of participant identification. Aggregated and anonymized results may be shared in scientific publications.

Locations