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Clinical Trial Details — Status: Completed

Administrative data

NCT number NCT03666338
Other study ID # SOMS-GCS
Secondary ID
Status Completed
Phase N/A
First received
Last updated
Start date July 11, 2011
Est. completion date February 4, 2016

Study information

Verified date September 2018
Source Technische Universität München
Contact n/a
Is FDA regulated No
Health authority
Study type Interventional

Clinical Trial Summary

Analysis of the randomized controlled SOMS trial of early, goal-directed mobilization to investigate if the treatment effect is consistent and independent of the initial conscious state without evidence of moderation or modification.


Recruitment information / eligibility

Status Completed
Enrollment 200
Est. completion date February 4, 2016
Est. primary completion date November 4, 2015
Accepts healthy volunteers No
Gender All
Age group 18 Years and older
Eligibility Inclusion Criteria:

- aged 18 years or older

- mechanically ventilated for less than 48 h and expected to require mechanical ventilation for at least another 24 h at the time of screening

- functionally independent at baseline with a Barthel Index Score of at least 70 at 2 weeks before admission to the ICU based on patient or proxy completion of the measure

Exclusion Criteria:

- admitted to hospital for more than 5 days before screening

- a motor component of Glasgow Coma Scale (GCS) lower than 5

- irreversible disorder with a 6-month mortality of greater than 50%,

- raised intracranial pressure

- cardiopulmonary arrest

- unstable fractures contributing to probable immobility

- inclusion in another trial at the same time

- acute myocardial infarction

- do not have lower part of their legs

- have a rapidly developing neuromuscluar disease

- pregnant

- ruptured or leaking aortic aneurysm

Study Design


Related Conditions & MeSH terms


Intervention

Other:
Early, goal-directed mobilization
Early, goal directed mobilization using (1) the SOMS algorithm and (2) facilitator

Locations

Country Name City State
n/a

Sponsors (4)

Lead Sponsor Collaborator
Technische Universität München Beth Israel Deaconess Medical Center, Massachusetts General Hospital, Università degli Studi di Brescia

References & Publications (1)

Schaller SJ, Anstey M, Blobner M, Edrich T, Grabitz SD, Gradwohl-Matis I, Heim M, Houle T, Kurth T, Latronico N, Lee J, Meyer MJ, Peponis T, Talmor D, Velmahos GC, Waak K, Walz JM, Zafonte R, Eikermann M; International Early SOMS-guided Mobilization Research Initiative. Early, goal-directed mobilisation in the surgical intensive care unit: a randomised controlled trial. Lancet. 2016 Oct 1;388(10052):1377-1388. doi: 10.1016/S0140-6736(16)31637-3. — View Citation

Outcome

Type Measure Description Time frame Safety issue
Primary Functional independence at hospital discharge minimal modified functional independence measure score of 8 (Scale ranging from 0-8 with the subdomain locomotion and transfer 0-4 each) At the day of hospital discharge, on average up to 1 month
Secondary average achieved mobility level during the ICU stay mean achieved SOMS level from ICU admission to ICU discharge, on average up to 2 weeks
Secondary Functional status at hospital discharge minimal modified functional independence measure score (range 0-8) of the subdomains transfer and locomotion with 0-4 each At the day of hospital discharge, on average up to 1 month
Secondary Start to mobilization (SOMS > 0) Start to mobilization in days (Surgical Optimal Mobilization Scale > 0, ranging from 0 = no mobilization to 4 ambulation) Days from ICU admission till first mobilization, approximately up to 5 days
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