Trial · NCT07886021
Impact of Functional Rehabilitation on Digital Independence: Validation of a Novel Smartphone Use Score as an Indicator of Discharge Readiness in Medical Care and Rehabilitation.
NCT07886021, Not applicable, Not yet recruiting, Artois Private Hospital
3 sourcestrials-2026-11-12-0.5.0
Cite this record
ConductScience Library. Impact of Functional Rehabilitation on Digital Independence: Validation of a Novel Smartphone Use Score as an Indicator of Discharge Readiness in Medical Care and Rehabilitation. Trials, record NCT07886021. Release trials-2026-11-12-0.5.0, 12 Nov 2026. https://conductscience.org/library/trials/NCT07886021
On this page
Trial
As registered on ClinicalTrials.gov, in the graph's capture of the registry.
- Title
- Impact of Functional Rehabilitation on Digital Independence: Validation of a Novel Smartphone Use Score as an Indicator of Discharge Readiness in Medical Care and Rehabilitation.
- NCT number
- NCT07886021
- Status
- Not yet recruiting
- Phases
- Not applicable
- Enrollment
- 150 participants, estimated
- Lead sponsor
- Artois Private Hospital
- Conditions
- Medical Rehabilitation
- Interventions
- TSHN-SMR (Test Standardisé d'Habileté Numérique sur Dispositif Dédié), Barthel scale
- First posted
- 2026-10-21
- Last updated
- 2026-10-21
Source ClinicalTrials.gov
Registered outcomes8
Each outcome the trial registered, primary first, in ClinicalTrials.gov's words.
| List | Outcome | Time frame | Description |
|---|---|---|---|
| Primary | Change in TSHN-SMR Total Score Between Admission and Discharge | Between admission and discharge from the SMR unit (average duration approximately 3 weeks, variable according to clinical condition) | Change in digital skills performance measured by the TSHN-SMR (Standardized Test of Digital Skills on a Dedicated Device) between admission and discharge from the SMR unit. |
| Secondary | Correlation between the TSHN-SMR score measured at discharge and the occurrence of rehospitalization within 3 months following discharge ( | Between admission and discharge from the SMR unit (average duration approximately 3 weeks, variable according to clinical condition) | (binary outcome: yes/no) Rehospitalization will be defined as any unplanned admission to a healthcare facility within 3 months after discharge from the SMR unit. The primary reason for rehospitalization will be collected when available from the medical record. |
| Secondary | Predictive performance of the discharge TSHN-SMR score, | Between admission and discharge from the SMR unit (average duration approximately 3 weeks, variable according to clinical condition) | Assessed using receiver operating characteristic (ROC) curve analysis and estimation of the area under the curve (AUC). |
| Secondary | Identification of a discharge TSHN-SMR score threshold | Between admission and discharge from the SMR unit (average duration approximately 3 weeks, variable according to clinical condition) | Identification of a discharge TSHN-SMR score threshold associated with an increased risk of rehospitalization. |
| Secondary | Correlation between the TSHN-SMR score (at admission and/or discharge) and patient characteristics | Between admission and discharge from the SMR unit (average duration approximately 3 weeks, variable according to clinical condition) | Relationships between the TSHN-SMR score (at admission and/or discharge) and patient characteristics, including age, Barthel Index score, and level of digital technology use. |
| Secondary | Inter-rater reliability of the TSHN-SMR score | Between admission and discharge from the SMR unit (average duration approximately 3 weeks, variable according to clinical condition) | Inter-rater reliability of the TSHN-SMR score, assessed by two independent evaluators. |
| Secondary | Correlation between the TSHN-SMR score and the Barthel Index | Between admission and discharge from the SMR unit (average duration approximately 3 weeks, variable according to clinical condition) | |
| Secondary | Correlation between the TSHN-SMR score and the level of digital technology use | Between admission and discharge from the SMR unit (average duration approximately 3 weeks, variable according to clinical condition) |
Source ClinicalTrials.gov
Outcomes0
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.
Tests0
The ConductCognition tests this trial's registered outcomes name, as ScienceGraph matched them in trial-tests-2026-11-12-0.2.1.
None in this release.
Data dates
The day each source was copied for this release.
Sources 3
- ClinicalTrials.gov's posted results, through CTTI's AACTFreely available. Acknowledgement requested
- ClinicalTrials.govNo license 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/NCT07886021
GET https://conductscience.org/api/trials/v1/NCT07886021/registered