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MIND Score for Prolonged Mechanical Ventilation

Psychometric Validation of the Multi-INdependency Dimensions (MIND) Score for Patients Under Prolonged Mechanical Ventilation

Status
Completed
Phases
Unknown
Study type
Observational
Source
ClinicalTrials.gov
Registry ID
NCT02255058
Acronym
MIND
Enrollment
129
Registered
2014-10-02
Start date
2014-08-31
Completion date
2015-02-28
Last updated
2015-03-02

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Functional Test, COPD, Neuromuscular Disorders, Mechanical Ventilation, Weaning, Disability

Brief summary

It was decided to develop a comprehensive disability score specifically designed for patients receiving prolonged mechanical ventilation (PMV); the collection of information included in the score should not impose any further intervention beyond what is routinely performed. So a new questionnaire was created (called the Multi-INdependency Dimensions (MIND) that included 3 sections (nurse, physiotherapist and medical doctor), 11 categories and 18 items. Each question was adapted to have a 5 item Likert scale. The primary objective of the study will be to evaluate the psychometric performance of the MIND score in terms of validity, reliability and sensitivity to change over time. The secondary objective will be to assess the inclusion of biological markers on the overall performance of the MIND score

Detailed description

Following recruitment all participants will be assessed by a medical doctor or respiratory therapist (trained on the study) who will fill out the MIND questionnaire on admission and make sure the other scales/questionnaires are also completed. On the same day of the collection of MIND, MRC score for quadriceps and biceps strength, Sequential Organ Failure Assessment (SOFA) score, Glasgow coma scale, Hospital Anxiety-depression scale (HADS), EuroQol-5D, Gussago Dependence Nursing Scale (GNS) will be also gathered. After 1 day and 30 days the MIND questionnaire will be also evaluated. Index of ADL-(Katz index) will be evaluated on discharge as well as weaning rate and survival. Sample Size Determination Based on the method of Rouquette A et al (1) we estimated a sample size of 200 patients to allow for the Rasch modelling to be applied. Statistical analysis Assessment of construct validity: Confirmation of the structure (e.g. multitrait analysis), clinical validity (comparison of disability score according to external clinical criteria) Assessment of reliability: Internal consistency reliability (using Cronbach's alpha), test-retest reliability (using intraclass correlations) Assessment of sensitivity to change over time: Comparison of change in disability score according to change in external clinical criteria Guidance for interpretation of disability score: Estimation of thresholds for patients' classification 1-Rouquette A, Falissard B Sample size requirements for the internal validation of psychiatric scales Int J Methods Psychiatr Res. 2011 Dec;20(4):235-49. doi: 10.1002/mpr.352. Epub 2011 Oct 24.

Interventions

OTHERNo intervention

The study is a Prospective observational cohort study

Sponsors

Linde AG
Lead SponsorINDUSTRY

Study design

Observational model
COHORT
Time perspective
PROSPECTIVE

Eligibility

Sex/Gender
ALL
Age
18 Years to 90 Years
Healthy volunteers
No

Inclusion criteria

* Adult patients with Prolonged mechanical Ventilation and a Diagnosis of Acute lung injury, COPD/Chronic Lung Disease, Neuromuscular Disorders, Post-Operative, Cardiovascular Disorders, Trauma, Other.

Exclusion criteria

* Expected length of stay \<48h, unable to achieve consent

Design outcomes

Primary

MeasureTime frame
To evaluate the psychometric performance of the MIND score in terms of validity, reliability and sensitivity to change over time6 Months

Secondary

MeasureTime frame
To assess the inclusion of biological markers on the overall performance of the MIND score6 Months

Countries

Argentina, Colombia, Germany

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 21, 2026