Trial · NCT07890688
Evaluation of the Effectiveness of Vision Care in Preventing Falls in Hospitalized Patients
NCT07890688, Not applicable, Not yet recruiting, Fundació Institut de Recerca de l'Hospital de la Santa Creu i Sant Pau
3 sourcestrials-2026-11-12-0.5.0
Cite this record
ConductScience Library. Evaluation of the Effectiveness of Vision Care in Preventing Falls in Hospitalized Patients. Trials, record NCT07890688. Release trials-2026-11-12-0.5.0, 12 Nov 2026. https://conductscience.org/library/trials/NCT07890688
On this page
Trial
As registered on ClinicalTrials.gov, in the graph's capture of the registry.
- Title
- Evaluation of the Effectiveness of Vision Care in Preventing Falls in Hospitalized Patients
- NCT number
- NCT07890688
- Status
- Not yet recruiting
- Phases
- Not applicable
- Enrollment
- 530 participants, estimated
- Lead sponsor
- Fundació Institut de Recerca de l'Hospital de la Santa Creu i Sant Pau
- Conditions
- Falls, Ulcer, Pressure
- Interventions
- Vision Care
- First posted
- 2026-10-22
- Last updated
- 2026-11-10
Source ClinicalTrials.gov
Registered outcomes7
Each outcome the trial registered, primary first, in ClinicalTrials.gov's words.
| List | Outcome | Time frame | Description |
|---|---|---|---|
| Primary | Incidence of falls during hospitalization | Through all the length of stay in the inpatient unit for each participant. From admission until discharge from the inpatient unit. Unit stay average of 11 days. | Number of falls occurring during hospitalization, according to the study definition of a fall. A fall is defined as an event resulting from an incident that causes a person to unintentionally come to rest on the ground or another lower level, including slips, trips, and loss of balance. |
| Secondary | Incidence of pressure ulcers | Through all the length of stay in the inpatient unit for each participant. From admission until discharge from the inpatient unit. Unit stay average of 11 days. | Occurrence of pressure ulcers of any stage during hospitalization, according to the classification system used by the hospital. |
| Secondary | Length of hospital stay | From admission until discharge from the inpatient unit. Unit stay average of 11 days. | Number of days from hospital admission to discharge from the inpatient unit. |
| Secondary | Healthcare professionals' satisfaction with the Vision Care device | At study completion, estimated at 6 months after recruitment initiation | Healthcare professionals' perceived usability, acceptability, and satisfaction with the use of the Vision Care device, assessed using an ad hoc brief questionnaire with 8 questions and a likert scale from 1 to 5 where higher scores mean better. |
| Secondary | Time to first fall | Through all the length of stay in the inpatient unit for each participant. From admission until discharge from the inpatient unit. Unit stay average of 11 days. | Time in days from hospital admission to the first fall during hospitalization. |
| Secondary | Performance of the Vision Care device | Through all the length of stay in the inpatient unit for each participant. From admission until discharge from the inpatient unit. Unit stay average of 11 days. | Assessment of the performance of the Vision Care device, including the number and type of alerts generated by the system, and response time to alerts. |
| Secondary | Safety of the Vision Care device | Through all the length of stay in the inpatient unit for each participant. From admission until discharge from the inpatient unit. Unit stay average of 11 days. | Assessment of the safety of the Vision Care device, including true positive alerts, false positive alerts and false negative alerts. |
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/NCT07890688
GET https://conductscience.org/api/trials/v1/NCT07890688/registered