Clinical Trials Logo

Clinical Trial Details — Status: Completed

Administrative data

NCT number NCT01270269
Other study ID # 101037
Secondary ID
Status Completed
Phase N/A
First received November 2, 2010
Last updated March 1, 2017
Start date February 2011
Est. completion date June 2014

Study information

Verified date March 2017
Source Vanderbilt University Medical Center
Contact n/a
Is FDA regulated No
Health authority
Study type Interventional

Clinical Trial Summary

Intensive care unit (ICU) hospitalization saves lives but often does so at a high personal cost to ICU survivors who frequently experience significant cognitive impairment and an array of physical and functional disabilities that limit their recovery and quality of life. While the problems experienced by these patients are likely amenable to rehabilitation, few ICU survivors receive focused rehabilitation. Recently, early physical rehabilitation in ICU patients has shown to improve the chances a patient will regain their pre-hospital functional status. Early cognitive rehabilitation for these patients has not yet been explored. This pilot study will determine the feasibility of early cognitive rehabilitation in ICU patients. The investigators will perform cognitive and physical rehabilitation, beginning in the earliest phases of critical illness, to determine the effect of these therapies on cognitive and functional outcomes in ICU survivors. The investigators hypothesize that combined cognitive and physical rehabilitation, started in the ICU, will improve recovery of cognitive and physical function as well as improve quality of life of ICU survivors.


Description:

The long-term consequences of critical illness and intensive care unit (ICU) hospitalization in ICU survivors are profound and include cognitive, physical, and functional impairments. The purpose of this study is to pilot test a multi-component, cognitive and physical rehabilitation program beginning in the ICU, combined with a 12-week home-based cognitive rehabilitation program following hospital discharge to determine whether participation in a rehabilitation program will result in improved outcomes among ICU survivors. The study will rely on a randomized controlled clinical trial design, with patients assigned to one of three groups: a "usual care" control group, an early physical activity group (without cognitive therapy), or an early cognitive therapy and physical activity group. All individuals in the intervention groups will receive protocolized physical therapy while hospitalized. In addition, individuals in the early cognitive therapy and physical activity group will receive cognitive therapy starting in the ICU and continuing for 12 weeks once a patient leaves the hospital. In-home visits will occur every other week during the 12-week intervention period.

The study's primary outcome is executive functioning (e.g. ability to plan, organize, multi-task) at 3-months following hospital discharge as measured by the Tower Test, a psychometric tool evaluating executive abilities. This has been chosen due to the fact that available research points to the presence of significant deficits in executive functioning among ICU survivors. Secondary outcomes include global cognitive function, physical function and Health Related Quality of Life by assessing scores on the following measures: Katz's ADL, Functional Activities Questionnaire, AD8, Short-Informant Questionnaire of Cognitive Decline in the Elderly, Clinical Dementia Rating Scale (if performed), Timed Up & Go test, Mini-Mental State Exam, Dysexecutive Questionnaire, Activities-Specific Balance Confidence Scale, Behavior Rating Inventory of Executive Function, Behavior Pain Inventory, Trails A & B test, Repeatable Battery for Assessment of Neuropsychological Status, General Employment Questionnaire, Beck Depression Inventory II, Post-traumatic stress checklist, Short Form 36, Canadian Study of Health and Aging and patient weight, and Tower Test score at 12 month follow-up. We will also track readmission to the hospital and admission to a nursing home or skilled rehabilitation facility as secondary outcomes during the 12-month follow-up period. The study duration will include 1 year of enrollment and 1 year for study completion following enrollment of the final patient.


Recruitment information / eligibility

Status Completed
Enrollment 87
Est. completion date June 2014
Est. primary completion date March 2013
Accepts healthy volunteers No
Gender All
Age group 18 Years and older
Eligibility Inclusion Criteria:

- Adult patients admitted to the medical or surgical ICU who are receiving treatment for respiratory failure, cardiogenic shock, hemorrhagic shock, and/or septic shock.

Exclusion Criteria:

- Moderate to severe dementia on ICU admission based on a standardized surrogate assessment (as this would prohibit patients from functioning independently at home);

- Moderate or severe physical dysfunction that precludes performance of independent activities of daily living based on a standardized surrogate assessment;

- Live greater than 120 miles from Nashville;

- Blind, deaf, or unable to speak English;

- Prisoners;

- Homelessness and no secondary contact person available

Study Design


Intervention

Behavioral:
Behavioral: Physical and functional rehabilitation
A multi-component program of physical rehabilitation interventions (without cognitive rehabilitation) will be delivered to patients beginning in the ICU and continue throughout the hospitalization.
Behavioral: Cognitive, physical, & functional rehabilitation
A multi-component program of cognitive, physical, and functional rehabilitation interventions will be delivered to patients beginning in the ICU with continued cognitive rehabilitation in their home environments over a focused 12-week period.

Locations

Country Name City State
United States Vanderbilt University Medical Center Nashville Tennessee

Sponsors (2)

Lead Sponsor Collaborator
Vanderbilt University Vanderbilt University Medical Center

Country where clinical trial is conducted

United States, 

References & Publications (4)

Brummel NE, Girard TD, Ely EW, Pandharipande PP, Morandi A, Hughes CG, Graves AJ, Shintani A, Murphy E, Work B, Pun BT, Boehm L, Gill TM, Dittus RS, Jackson JC. Feasibility and safety of early combined cognitive and physical therapy for critically ill med — View Citation

Brummel NE, Jackson JC, Girard TD, Pandharipande PP, Schiro E, Work B, Pun BT, Boehm L, Gill TM, Ely EW. A combined early cognitive and physical rehabilitation program for people who are critically ill: the activity and cognitive therapy in the intensive care unit (ACT-ICU) trial. Phys Ther. 2012 Dec;92(12):1580-92. doi: 10.2522/ptj.20110414. — View Citation

Jackson JC, Ely EW, Morey MC, Anderson VM, Denne LB, Clune J, Siebert CS, Archer KR, Torres R, Janz D, Schiro E, Jones J, Shintani AK, Levine B, Pun BT, Thompson J, Brummel NE, Hoenig H. Cognitive and physical rehabilitation of intensive care unit survivors: results of the RETURN randomized controlled pilot investigation. Crit Care Med. 2012 Apr;40(4):1088-97. doi: 10.1097/CCM.0b013e3182373115. — View Citation

Schweickert WD, Herlitz J, Pohlman AS, Gehlbach BK, Hall JB, Kress JP. A randomized, controlled trial evaluating postinsertion neck ultrasound in peripherally inserted central catheter procedures. Crit Care Med. 2009 Apr;37(4):1217-21. doi: 10.1097/CCM.0b013e31819cee7f. — View Citation

Outcome

Type Measure Description Time frame Safety issue
Primary Tower Test A psychometric measure of executive functioning. 3 months post hospital discharge
Secondary Timed Up and Go (TUG) A timed test assessing physical strength and gait speed. 3 months post hospital discharge
Secondary Functional Activities Questionnaire A brief measure of higher order (IADL) functioning. 3 months post hospital discharge
Secondary EQ-5 Global Scores The EQ-5 Global Scores is an assessment of quality of life. 3 months post hospital discharge
Secondary Katz Activities of Daily Living (ADL) scale A six-item tool assessing the degree of independence vs. dependence in basic activities of daily living. 3 months post hospital discharge
Secondary Activities-Specific Balance Confidence Scale (ABC) A brief rating scale that asks participants to rate how confident they are that they can maintain their balance and remain steady while engaged in 16 non-hazardous tasks. 3 months post hospital discharge
Secondary AD8 A brief surrogate or patient based measure that assesses recent change in a variety of cognitive abilities. 3 months post hospital discharge
Secondary Short-Informant Questionnaire of Cognitive Decline in the Elderly (Short IQCODE) A measure of cognitive functioning that evaluates the degree of decline from baseline and which is complementary to the AD8. This measure will only be used in patients over the age of 50 who had any problems with memory or thinking prior to current illness. 3 months post hospital discharge
Secondary Mini Mental State Exam (MMSE) A widely used measure of overall cognitive functioning that briefly samples abilities in a wide array of areas including memory and attention. 3 months post hospital discharge
Secondary Dysexecutive Questionnaire (Dys Exec) A questionnaire, which has both patient and surrogate versions, that assesses patient functioning in a number of functional areas sensitive to executive dysfunction. 3 months post hospital discharge
Secondary TRAILS A & B Test Two widely used to test the speed that it takes to connect a series of numbers (Part A) and numbers alternating with letters (Part B). 3 months post hospital discharge
Secondary General and Employment Questionnaire A brief series of questions which pertain to patient history and demographics and which also inquire about employment both before and after ICU hospitalization. 3 months post hospital discharge
Secondary Canadian Study of Health and Aging (CHSA) Frailty Scale A brief global rating scale of frailty based on clinical impression. 3 months post hospital discharge
Secondary Tower Test A psychometric measure of executive functioning. 12 months post hospital discharge
Secondary Timed Up and Go (TUG) A timed test assessing physical strength and gait speed. 12 months post hospital discharge
Secondary Functional Activities Questionnaire A brief measure of higher order (IADL) functioning. 12 months post-hospital discharge
Secondary EQ-5 Global Scores The EQ-5 Global Scores is an assessment of quality of life. 12 months post hospital discharge
Secondary Katz Activities of Daily Living (ADL) scale A six-item tool assessing the degree of independence vs. dependence in basic activities of daily living. 12 months post hospital discharge
Secondary Activities-Specific Balance Confidence Scale (ABC) A brief rating scale that asks participants to rate how confident they are that they can maintain their balance and remain steady while engaged in 16 non-hazardous tasks. 12 months post hospital discharge
Secondary AD8 A brief surrogate or patient based measure that assesses recent change in a variety of cognitive abilities. 12 months post hospital discharge
Secondary Short-Informant Questionnaire of Cognitive Decline in the Elderly (Short IQCODE) A measure of cognitive functioning that evaluates the degree of decline from baseline and which is complementary to the AD8. This measure will only be used in patients over the age of 50 who had any problems with memory or thinking prior to current illness. 12 months post hospital discharge
Secondary Mini Mental State Exam (MMSE) A widely used measure of overall cognitive functioning that briefly samples abilities in a wide array of areas including memory and attention. 12 months post hospital discharge
Secondary Dysexecutive Questionnaire (Dys Exec) A questionnaire, which has both patient and surrogate versions, that assesses patient functioning in a number of functional areas sensitive to executive dysfunction. 12 months post hospital discharge
Secondary TRAILS A & B Test Two widely used to test the speed that it takes to connect a series of numbers (Part A) and numbers alternating with letters (Part B). 12 months post hospital discharge
Secondary General and Employment Questionnaire A brief series of questions which pertain to patient history and demographics and which also inquire about employment both before and after ICU hospitalization. 12 months post hospital discharge
Secondary Canadian Study of Health and Aging (CHSA) Frailty Scale A brief global rating scale of frailty based on clinical impression. 12 months post hospital discharge
Secondary Mortality 2 months post hospital discharge
Secondary Rehospitalization rate and number of hospital days 12 months post hospital discharge
See also
  Status Clinical Trial Phase
Completed NCT05686486 - Gentle Gymnastics and Relationship Between Family Caregivers and Residents With Dementia in Nursing Homes N/A
Terminated NCT05451693 - Outreach-ER: A Dementia Care Intervention Program
Recruiting NCT05820919 - Enhancing Sleep Quality for Nursing Home Residents With Dementia - R33 Phase N/A
Enrolling by invitation NCT06040294 - Dementia and Disability Simulation for College Nursing Students' Senior Activity Facilitation Skills N/A
Completed NCT05114187 - An Internet-Based Education Program for Care Partners of People Living With Dementia N/A
Recruiting NCT06322121 - Vascular Aspects in Dementia: Part 2
Active, not recruiting NCT03676881 - Longitudinal Validation of a Computerized Cognitive Battery (Cognigram) in the Diagnosis of Mild Cognitive Impairment and Alzheimer's Disease
Completed NCT04426838 - Cognitive Behavioral Therapy for Insomnia for the Dementia Caregiving Dyad N/A
Recruiting NCT03462485 - Pilot Study of the Effects of Playing Golf on People With Dementia N/A
Active, not recruiting NCT03677284 - Managing Time With Dementia: Effects of Time Assistive Products in People With Dementia N/A
Completed NCT03849937 - Changing Talk Online (CHATO) Study N/A
Recruiting NCT06284213 - Biomarkers for Vascular Contributions to Cognitive Impairment and Dementia Consortium
Recruiting NCT05579236 - Cortical Disarray Measurement in Mild Cognitive Impairment and Alzheimer's Disease
Completed NCT05080777 - Pilot Pragmatic Clinical Trial to Embed Tele-Savvy Into Health Care Systems N/A
Completed NCT04571697 - A Study of Comparing Rates of Dementia and Alzheimer's Disease in Participants Initiating Methotrexate Versus Those Initiating Anti-tumor Necrosis Factor (TNF)-Alpha Therapy
Completed NCT03583879 - Using Gait Robotics to Improve Symptoms of Parkinson's Disease N/A
Recruiting NCT06033066 - Financial Incentives and Recruitment to the APT Webstudy N/A
Active, not recruiting NCT05204940 - Longitudinal Observational Biomarker Study
Recruiting NCT05684783 - Dementia Champions in Homecare
Completed NCT03147222 - Function Focused Care: Fracture Care at Home N/A