Trial · NCT05900778
Implementation of a HABIT-ILE Intervention at William Lennox Neurological Hospital (NeuREHA)
NCT05900778, Not applicable, Recruiting, Université Catholique de Louvain
3 sourcestrials-2026-11-12-0.4.0
Cite this record
ConductScience Library. Implementation of a HABIT-ILE Intervention at William Lennox Neurological Hospital (NeuREHA). Trials, record NCT05900778. Release trials-2026-11-12-0.4.0, 12 Nov 2026. https://conductscience.org/library/trials/NCT05900778
On this page
Trial
As registered on ClinicalTrials.gov, in the graph's capture of the registry.
- Title
- Implementation of a HABIT-ILE Intervention at William Lennox Neurological Hospital (NeuREHA)
- NCT number
- NCT05900778
- Status
- Recruiting
- Phases
- Not applicable
- Enrollment
- 40 participants, estimated
- Lead sponsor
- Université Catholique de Louvain
- Conditions
- Acquired Brain Injury
- Interventions
- HABIT-ILE, Conventional intervention
- First posted
- 2023-06-13
- Last updated
- 2023-06-18
Source ClinicalTrials.gov
Registered outcomes16
Each outcome the trial registered, primary first, in ClinicalTrials.gov's words.
| List | Outcome | Time frame | Description |
|---|---|---|---|
| Primary | Flanker task | T0 (baseline), T1 (after 2weeks intervention), T2(3 months follow-up) | Cognitive functions of the children will be assessed by Flanker task. |
| Primary | Changes in Gross Motor Function Measurement (GMFM 66) | T0 (baseline), T1 (after 2weeks intervention), T2(3 months follow-up) | The GMFM has been developed to measure the change in gross motor function over time in children with cerebral palsy. |
| Secondary | Changes in isometric muscular strength (Jamar) | T0 (baseline), T1 (after 2weeks intervention), T2(3 months follow-up) | A quantitative and objective measure of isometric muscular strength of hand and forearm. |
| Secondary | Stroop task | T0 (baseline), T1 (after 2weeks intervention), T2(3 months follow-up) | Executive functions of the children will be assessed by Stroop task. |
| Secondary | Changes in unimanual dexterity: Box and Blocks test (BBT) | T0 (baseline), T1 (after 2weeks intervention), T2(3 months follow-up) | The BBT is a test of gross manual dexterity. Each hand is tested individually and the BBT is scored through the number of blocks carried over the partition from one part to another part of a box during the one-minute trial period. |
| Secondary | Changes on bimanual function (Assisting Hand Assessment (AHA)) | T0 (baseline), T1 (after 2weeks intervention), T2(3 months follow-up) | Developed to observe the efficacy of the assisting hand use, in children with unilateral cerebral palsy (scored in percentage), during bimanual activities for the randomized controlled trial |
| Secondary | Changes in 6 Minutes Walking Test (6MWT) | T0 (baseline), T1 (after 2weeks intervention), T2(3 months follow-up) | The 6 Minutes Walking Test measures the distance that the patient walk as much as possible within a period of 6-minutes in a 30 meters long corridor. |
| Secondary | Changes in Pediatric balance scale (PBS) | T0 (baseline), T1 (after 2weeks intervention), T2(3 months follow-up) | A 14-item criterion-referencekd measure that examines functional balance in the context of everyday tasks in the pediatric population. |
| Secondary | Changes in Canadian Occupational Performance Measure (COPM) | T0 (baseline), T1 (after 2weeks intervention), T2(3 months follow-up) | This is an interview-setting designed to capture a patient's self-perception of performance and satisfaction of it in everyday activities, observed over time. During the interview, parents set up 5 activities considered difficult in daily life. These are then assessed, in a 1 to 10 scale, regarding the child's self-perception of performance and satisfaction of it. The total score is the average of the scores for perception and satisfaction separately (score from 1 to 10; higher score means better performance/satisfaction) |
| Secondary | Changes in ACTIVLIM-CP questionnaire | T0 (baseline), T1 (after 2weeks intervention), T2(3 months follow-up) | This parent's filled questionnaire measures a patient's ability to perform daily activities requiring the use of the upper and/or the lower extremities through 43 items specific to patients with cerebral palsy. It ranges from - 7 to +7 logits (higher score means better performance). |
1 to 10 of 16Source ClinicalTrials.gov
See all 16 registered outcomesOutcomes0
Each outcome the trial posted results for, in ClinicalTrials.gov's words.
None in this release.
Results by group0
Each measurement the trial posted, group by group, in the words and numbers it posted.
None in this release.
Participant flow0
How many started, completed or left each group, period by period.
None in this release.
Adverse events0
Each adverse event the trial posted, group by group: the participants affected out of those at risk.
None in this release.
Adverse event totals0
The totals the trial posted for each group.
None in this release.
Papers0
The papers the trial lists on ClinicalTrials.gov.
None in this release.
Grants0
The grants NIH RePORTER links to the trial, newest funded first: NIH's, and some of AHRQ's, CDC's, FDA's and VA's. Each shows its title, principal investigators, organization and funder in its newest year.
None in this release.
Trial comparisons0
Comparisons of the trial's two groups, calculated by ConductScience from the counts it posted.
None in this release.
Tests2
The ConductCognition tests this trial's registered outcomes name, as ScienceGraph matched them in trial-tests-2026-11-12-0.2.1.
| Test | Named as | Source |
|---|---|---|
| Eriksen Flanker Task | Primary outcome | ConductCognition |
| Stroop Color-Word Test | Secondary outcome | ConductCognition |
Source
- Release
- trials-2026-11-12-0.4.0
- Release manifest SHA-256
- 0f4a8d8c48aee2a7573ae0fa94ecbeab70c1adbe449bbc95c424bc7d3e97b9d4
- Registry capture
- 2026-11-12
- Results copy, AACT
- 2026-03-23
- NIH clinical studies file
- 2026-11-13
Source ClinicalTrials.gov
Sources 3
- ClinicalTrials.gov's posted results, through CTTI's AACTFreely available. Acknowledgement requested
- ClinicalTrials.govNone stated
- NIH RePORTER's clinical studies and project filesPublic domain
Each source's terms
- ClinicalTrials.gov's posted results, through CTTI's AACTClinicalTrials.gov data via Aggregate Analysis of ClinicalTrials.gov (AACT), CTTI. CTTI makes its materials freely available and requests acknowledgement. https://aact.ctti-clinicaltrials.org/documentation/299
- ClinicalTrials.govnone stated
- NIH RePORTER's clinical studies and project filesPublic domain (NIH RePORTER)
ClinicalTrials.gov's data carry an international copyright outside the United States: https://clinicaltrials.gov/about-site/terms-conditions.
For software
Read this trial from software.
The record and each of its lists are JSON, twenty rows a page. No key.
GET https://conductscience.org/api/trials/v1/NCT05900778
GET https://conductscience.org/api/trials/v1/NCT05900778/registered