Evaluation of the Triage Risk Screening Tool (TRST-U)
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| ClinicalTrials.gov Identifier: NCT03544957 |
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Recruitment Status :
Completed
First Posted : June 4, 2018
Last Update Posted : August 28, 2019
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| Condition or disease |
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| Elderly Subject Fragility |
A constant increase of emergencies admission of elderly subjects is registered. The current problem is the identification and early screening of these patients upon admission at the accident and emergency department for early tracking in geriatric network. This early assessment could allow a shorter waiting time, a better orientation of patients and a decrease in the number of re-hospitalization.
There are many screening process for fragility tests but there seem to be nonspecifically. The advantage of TRST is its simplicity and speed of filling.
In 2015, Duc et al. have found that TRST may be a screening instrument for elderly subject and is going to require geriatric mobile team (GMT) for evaluation. Unfortunately, the threshold may be too sensitive and GMT solicitation is too high.
| Study Type : | Observational |
| Actual Enrollment : | 199 participants |
| Observational Model: | Cohort |
| Time Perspective: | Prospective |
| Official Title: | Evaluation of the Triage Risk Screening Tool (TRST) as Screening Instrument Elderly Subject Fragility at the Accident and Emergency Department |
| Actual Study Start Date : | October 1, 2018 |
| Actual Primary Completion Date : | January 1, 2019 |
| Actual Study Completion Date : | April 1, 2019 |
- TRST-U [ Time Frame: Day 1 ]Triage Risk Screening Tool completed by an emergency doctor
- TRST-G [ Time Frame: Day 1 ]Triage Risk Screening Tool completed by a geriatrician
- SEGA instrument [ Time Frame: Day 1 ]Evaluation of TRST versus SEGA instrument (gold standard)
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| Ages Eligible for Study: | 75 Years and older (Older Adult) |
| Sexes Eligible for Study: | All |
| Accepts Healthy Volunteers: | No |
| Sampling Method: | Non-Probability Sample |
Inclusion Criteria:
- Patients who are more than 75 years old
- Admitted to the emergency department for medical or surgical reason
- Admitted from Monday to Friday (8h30 AM- 6h PM)
Exclusion Criteria:
- Patient with specific care (vital emergency, urgent surgery)
- Patient or his support person opposing the use of data
To learn more about this study, you or your doctor may contact the study research staff using the contact information provided by the sponsor.
Please refer to this study by its ClinicalTrials.gov identifier (NCT number): NCT03544957
| France | |
| CHR Metz Thionville | |
| Metz, Moselle, France, 57085 | |
| Responsible Party: | Centre Hospitalier Régional Metz-Thionville |
| ClinicalTrials.gov Identifier: | NCT03544957 |
| Other Study ID Numbers: |
2018-02Obs-CHRMT |
| First Posted: | June 4, 2018 Key Record Dates |
| Last Update Posted: | August 28, 2019 |
| Last Verified: | April 2018 |
| Individual Participant Data (IPD) Sharing Statement: | |
| Plan to Share IPD: | No |
| Studies a U.S. FDA-regulated Drug Product: | No |
| Studies a U.S. FDA-regulated Device Product: | No |
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Screening instrument |

