Impact of the "Kid'EM App" Digital Guidance Tool for Setting Rehabilitation Goals by the Rehabilitation Professional for Children with Chronic Conditions Impacting Physical Health (READ'APP'T)
Condition(s) studied
Investigational drug(s) / intervention(s)
Kid'EM app" experimental group: In the "Kid'EM app" experimental group arm, only the application used differs. Visits are organized in the same way as in the controle app arm. Visit 0 (Inclusion) + Visit 1 (V1) : Physical visit Children are included in the study by the investigator, formalized by signing a consent form. Parents fill in questionnaires Visit 2 (when 1st objective is set): Telephone interview to assess performance and satisfaction levels after the first goal has been set. Visit 3 (when setting the 2nd goal): Telephone interview to assess performance and satisfaction levels after the second goal has been set. Visit 4 (week 14 - end of study): Physical visit The questionnaires are again completed by the parents, either directly on a tablet or on paper for later input. Visit 4 bis: Telephone interview to assess performance and satisfaction levels after the work on the first two objectives. Visit 5 (focus group, optional post-study visit)
Kid'EM app control group: Use of control application without guidance for goal setting Visit 0 (Inclusion) + Visit 1 (V1) : Physical visit Children are included in the study by the investigator, formalized by signing a consent form. Parents fill in questionnaires Visit 2 (when 1st objective is set): Telephone interview to assess performance and satisfaction levels after the first goal has been set. Visit 3 (when setting the 2nd goal): Telephone interview to assess performance and satisfaction levels after the second goal has been set. Visit 4 (week 14 - end of study): Physical visit The questionnaires are again completed by the parents, either directly on a tablet or on paper for later input. Visit 4 bis: Telephone interview to assess performance and satisfaction levels after the work on the first two objectives. Visit 5 (focus group, optional post-study visit)
Study summary
On an individual level, the first expected benefit for the child using the "Kid'EM app" would be an improvement in the quality of his or her rehabilitation goals, which would be more Specific, Measurable, Activity-related, Realistic and Time-defined (SMART). A second expected benefit for the child, thanks to the work carried out in rehabilitation sessions on objectives adapted to his or her needs and day-to-day life, encouraging commitment and motivation, would be to improve the effectiveness of the care offered to him or her, thereby enhancing autonomy and physical health. For parents, taking part in goal-setting, by contributing their knowledge of their child and his or her daily life, would increase their involvement in their child's care and improve their satisfaction with the care offered. By setting SMART functional goals and facilitating communication between therapist, child and family, we expect to see a more child- and family-centred approach to care.
On a collective level, the "Kid'EM app" proposal would, as recommended by the WHO, improve professional rehabilitation practices and facilitate convergence towards good clinical practices for professionals (physiotherapists, occupational therapists, PRMs, etc.), thereby increasing the efficiency of the child rehabilitation care system.
If its value is demonstrated, the Kid'EM app could be adapted for children with other chronic illnesses requiring non-motor rehabilitation follow-up. The digitization of this goal-setting tool means that this low-cost practice could be widely disseminated.
Eligibility
Primary outcome measure(s)
- Quality of the first two objectives set for each child during the 12-week 'Kid'EM app' or 'app control' period — Up to 3 weeks
Quality, adequate or not (binary criterion, measured with the SMART goal evaluation method: SMART GEM), of the first two goals set for each child during the 12-week period of use of the "Kid'EM app" or "control app". - Quality of the first two objectives set for each child during the 12-week 'Kid'EM app' or 'app control' period — From week 14 to week 16
Quality, adequate or not (binary criterion, measured with the SMART goal evaluation method: SMART GEM), of the first two goals set for each child during the 12-week period of use of the "Kid'EM app" or "control app".
Trial sites (36)
| Facility | City | Region | Status |
|---|---|---|---|
| Ildys Ty Yann | Angers | France | |
| Les Capucins Angers | Angers | France | |
| IEM Galaxie | Argeles | France | |
| SESSAD 93 - Aulnay | Aulnay-sous-Bois | France | |
| SESSAD APF Basse Goulaine | Basse-Goulaine | France | |
| SMR Concarneau | Concarneau | France | |
| Dispositif sensoriel et moteur Clos Chauveau - DIJON | Dijon | France | |
| Sessad APF France Handicap du Finistère | Gouesnou | France | |
| CAMSP APF Grenoble | Grenoble | France | |
| Cabinet de Kinésithérapie - Elodie CREACH | Landerneau | France | |
| SESSAD 93-Raincy | Le Raincy | France | |
| Cabinet d'Ergothérapie - Maison des Korrigans | Lesneven | France | |
| SESSAD A Denn Askell - KERPAPE | Lorient | France | |
| CAMSP Nelson Mandela | Lyon | France | |
| CAPEDIA | Lyon | France | |
| CMCR Les Massues | Lyon | France | |
| CMRP Romans Ferrari - Service Brulologie | Miribel | France | |
| CMRP Romans Ferrari - Service Neurologie | Miribel | France | |
| IEM La Marrière | Nantes | France | |
| CHU Carémeau | Nîmes | France | |
| Cabinet Jaures Kiné | Nîmes | France | |
| Cabinet Sophie CHAPELLIER | Nîmes | France | |
| IEM La Cigale | Nîmes | France | |
| SESSAD La Cigale | Nîmes | France | |
| IEM Ar Menn | Ploemeur | France | |
| Centre Paul DOTTIN | Ramonville-Saint-Agne | France | |
| SESSAD Henri Matisse | Rennes | France | |
| SESSAD Romans | Romans-sur-Isère | France | |
| SMR pédiatrique ILDYS | Roscoff | France | |
| SESSAD Saint Etienne | Saint-Etienne | France | |
| CHU Saint Etienne - MPR Pédiatrique | Saint-Etienne | France | |
| CMPR Côte d'Amour | Saint-Nazaire | France | |
| Centre de l'Arche | Saint-Saturnin | France | |
| UGECAM Strasbourg | Strasbourg | France | |
| SMR Vannes - Centre hospitalier bretagne atlantique | Vannes | France | |
| Sessad Apf Voiron | Voiron | France |
More University Hospital, Brest trials in France
This page summarises publicly available registry data for informational purposes — not medical advice. Eligibility is determined by each study team; patients should discuss participation with their clinician.
View NCT06475950 on ClinicalTrials.gov ↗ ← All trials in France