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Study of Intensive Care Unit (ICU)-Acquired Weakness (Handgrip Strength Study)

Clinical Determinants of Handgrip Strength in Critically Ill Adults: Pilot Study

Status
Completed
Phases
Unknown
Study type
Observational
Source
ClinicalTrials.gov
Registry ID
NCT00702000
Enrollment
49
Registered
2008-06-19
Start date
2008-05-31
Completion date
2010-05-31
Last updated
2016-01-18

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

Conditions

Peripheral Muscle Strength

Keywords

ICU acquired paresis

Brief summary

To better understand ICU-acquired weakness in patients requiring mechanical ventilation in the Intensive Care Unit.

Detailed description

We have generated the hypothesis that handgrip strength can be used to develop our understanding of the effects of critical illness on peripheral muscle strength. To begin to develop this hypothesis, a better understanding of the determinants of handgrip strength needs to be developed. As a result we propose to perform a prospective observational study examining the clinical factors that are associated with handgrip strength. Several clinical factors are known to be associated with increased risk of developing ICUAP while hospitalized: multiple organ failure, severe sepsis, female gender and treatments like steroids. As many of these risk factors are not modifiable, the opportunity to intervene is unclear. However, by attempting to better describe the spectrum of strength deficits experienced by critically ill patients we may better be able to dissect and prevent ICUAP.

Interventions

None listed

Sponsors

Naeem Ali, MD
Lead SponsorOTHER

Study design

Observational model
CASE_ONLY
Time perspective
PROSPECTIVE

Eligibility

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

Inclusion criteria

* • Adult patients admitted to the Medical ICU * Age ≥ 18 years of age at ICU admit. * Requiring mechanical ventilation for at least 24 hours

Exclusion criteria

* • Moribund or in the process of withdrawal of life support * Patient, family or physicians not in favor of continued support until awakening. * Profound neurologic injury associated with little or no chance of awakening. * Active consideration of a diagnosis of brain death by treating physicians. * Known history of chronic neurological disease resulting in muscle weakness in more than two limbs. * Inability to perform handgrip dynamometry prior to acute illness. * Subject is a Non-english speaker * Subject or surrogate unable to provide informed consent. * ICU stay of greater than 24 hours within the last thirty days or at any point during the current hospitalization * Greater than seven days of hospital care prior to hospital admission. * Greater than five days since inclusion criteria met.

Design outcomes

Primary

MeasureTime frame
To determine the feasibility of performing serial assessments of strength (handgrip and limb muscle strength) in a broad population of critically ill patients.duration of ICU stay-up to 10 days

Secondary

MeasureTime frame
To determine the acute medical illnesses associated with weaknessduration of ICU stay-up to 10 days
To determine the modifiable risk factors associated with weaknessduration of ICU stay-up to 10 days
To determine if there is an association between handgrip strength and ICUAP riskduration of ICU stay-up to 10 days
To generate a set of normative data for handgrip strength in critically ill patients adjusting for important non-modifiable risk factorsduration of ICU stay-up to 10 days

Countries

United States

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 4, 2026