Comparison of Subacute and Hospital Based Rehabilitation Care

NCT00038363 · Status: COMPLETED · Phase: PHASE2 · Type: INTERVENTIONAL · Enrollment: 260

Last updated 2009-01-21

No results posted yet for this study

Summary

The proposed study objective is to compare hospital-based rehabilitative care with transitional subacute rehabilitation for adults recently diagnosed with a disabling disorder. Clinical outcomes, cost and utilization of services will be compared in order to test the hypotheses that medically-stable patients receiving rehabilitation from subacute care facilities will: 1) function as well physically, 2) report less family dysfunction, 3) have better psychological adjustment and well-being than controls who receive only hospital-based inpatient care, and 4) receive services at lower cost. We intend to assess the impact of hospital-based versus subacute care on clinical and cost outcomes at admission, discharge \[3 months post-admission\] and at 12 months. The first set of analyses will determine predictors of physical function, family function, psychological adjustment and well-being over a 1 year period.

Conditions

  • Aging

Interventions

PROCEDURE

Rehabilitation

PROCEDURE

Subacute care

Sponsors & Collaborators

Principal Investigators

  • David Wolff, Ph.D. Special Assistant to the Director · Program Analysis and Review Section (PARS), VA Rehabilitation Research & Development Service

  • Vicki Mongiardo, Program Analyst · Program Analysis and Review Section (PARS), VA Rehabilitation Research and Development Service

Study Design

Allocation
RANDOMIZED
Purpose
TREATMENT
Masking
SINGLE
Model
FACTORIAL

Eligibility

Min Age
18 Years
Sex
ALL
Healthy Volunteers
No

Timeline & Regulatory

Start
2001-04-30
Completion
2004-03-31

Countries

  • United States

Study Locations

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Entities

Read the full study record

This page highlights key information. For complete eligibility criteria, study locations, investigator contacts, and the full protocol, visit the original record on ClinicalTrials.gov.

View NCT00038363 on ClinicalTrials.gov