Trial · NCT07907237
Feasibility Study on the Use of a Walking Exoskeleton in the Intensive Care Unit
NCT07907237, Not applicable, Not yet recruiting, CHU de Reims
3 sourcestrials-2026-11-12-0.5.0
Cite this record
ConductScience Library. Feasibility Study on the Use of a Walking Exoskeleton in the Intensive Care Unit. Trials, record NCT07907237. Release trials-2026-11-12-0.5.0, 12 Nov 2026. https://conductscience.org/library/trials/NCT07907237
On this page
Trial
As registered on ClinicalTrials.gov, in the graph's capture of the registry.
- Title
- Feasibility Study on the Use of a Walking Exoskeleton in the Intensive Care Unit
- NCT number
- NCT07907237
- Status
- Not yet recruiting
- Phases
- Not applicable
- Enrollment
- 30 participants, estimated
- Lead sponsor
- CHU de Reims
- Conditions
- Neuromuscular Disease in Post-Intensive Care Syndrome
- Interventions
- rehabilitation session assisted by an exoskeleton
- First posted
- 2026-10-30
- Last updated
- 2026-10-30
Source ClinicalTrials.gov
Registered outcomes23
Each outcome the trial registered, primary first, in ClinicalTrials.gov's words.
| List | Outcome | Time frame | Description |
|---|---|---|---|
| Primary | Feasibility of Exoskeleton-Assisted Rehabilitation | Up to 14 days | Eligibility rate, defined as the number of eligible participants relative to the number of patients in the ICU |
| Primary | Feasibility of Exoskeleton-Assisted Rehabilitation | Up to 14 days | Enrollment rate, defined as the number of participants enrolled in the study relative to the number of eligible patients |
| Primary | Feasibility of Exoskeleton-Assisted Rehabilitation | Up to 14 days | Initiation rate, defined as the number of included participants who complete at least one session |
| Primary | Feasibility of Exoskeleton-Assisted Rehabilitation | Up to 14 days | Number of completed sessions |
| Primary | Feasibility of Exoskeleton-Assisted Rehabilitation | Up to 14 days | Setup and session duration |
| Primary | Feasibility of Exoskeleton-Assisted Rehabilitation | Up to 14 days | Rate of completed sessions relative to the number of scheduled sessions |
| Primary | Feasibility of Exoskeleton-Assisted Rehabilitation | Up to 14 days | Technical failure rate (malfunction, calibration difficulties, anatomical incompatibility) |
| Primary | Feasibility of Exoskeleton-Assisted Rehabilitation | Up to 14 days | Reasons for session termination |
| Secondary | Patient acceptability | Up to 14 days | number of initial refusals |
| Secondary | Patient acceptability | Up to 14 days | the dropout rate |
1 to 10 of 23Source ClinicalTrials.gov
See all 23 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.
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/NCT07907237
GET https://conductscience.org/api/trials/v1/NCT07907237/registered?page=2