- ICH GCP
- US Clinical Trials Registry
- Clinical Trial NCT00718107
Satisfaction Survey for Amyotrophic Lateral Sclerosis (ALS) Patients Comparing Rooms With and Without Assistive Technology
March 1, 2013 updated by: Drexel University College of Medicine
Satisfaction Survey for ALS Patients Comparing Rooms With and Without Assistive Technology
The purpose of this study is :
- To assess the ALS patient's satisfaction related to a hospital stay on the neurology floor of Hahnemann Hospital.
- To compare the reported satisfaction of those individuals who stayed in a standard hospital room with those who stayed in Room 1455. Room 1455 is a room specifically set up with assistive technology related to environmental controls for individuals with disabilities.
- To look at frequency of use of the various pieces of adaptive equipment.
Study Overview
Status
Terminated
Study Type
Observational
Enrollment (Actual)
5
Contacts and Locations
This section provides the contact details for those conducting the study, and information on where this study is being conducted.
Study Locations
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Pennsylvania
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Philadelphia, Pennsylvania, United States, 19107
- MDA/ALS Center of Hope
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Participation Criteria
Researchers look for people who fit a certain description, called eligibility criteria. Some examples of these criteria are a person's general health condition or prior treatments.
Eligibility Criteria
Ages Eligible for Study
18 years to 90 years (Adult, Older Adult)
Accepts Healthy Volunteers
No
Genders Eligible for Study
All
Sampling Method
Non-Probability Sample
Study Population
In-patients from the neurology floor of Hahnemann Hospital
Description
Inclusion Criteria:
- In-patients with probable or definite ALS, ages 18 - 90, staying on the neurology floor of Hahnemann Hospital
Exclusion Criteria:
- In-patients who do not meet the criteria of the diagnosis of ALS.
Study Plan
This section provides details of the study plan, including how the study is designed and what the study is measuring.
How is the study designed?
Design Details
Cohorts and Interventions
Group / Cohort |
|---|
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ALS
Subjects having either definite or probable ALS by El Escorial Criteria.
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What is the study measuring?
Primary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
|---|---|---|
|
Patient Satisfaction
Time Frame: Period of Hospital Stay
|
Survey administered asks patients to rate their satisfaction with their hospital stay from Very Dissatisfied to Very Satisfied.
Specific questions included satisfaction with hospital staff, quality of care, and comfort and accessibility of their room.
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Period of Hospital Stay
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Collaborators and Investigators
This is where you will find people and organizations involved with this study.
Collaborators
Study record dates
These dates track the progress of study record and summary results submissions to ClinicalTrials.gov. Study records and reported results are reviewed by the National Library of Medicine (NLM) to make sure they meet specific quality control standards before being posted on the public website.
Study Major Dates
Study Start
June 1, 2005
Primary Completion (Actual)
February 1, 2012
Study Completion (Actual)
February 1, 2012
Study Registration Dates
First Submitted
July 14, 2008
First Submitted That Met QC Criteria
July 16, 2008
First Posted (Estimate)
July 18, 2008
Study Record Updates
Last Update Posted (Estimate)
March 5, 2013
Last Update Submitted That Met QC Criteria
March 1, 2013
Last Verified
March 1, 2013
More Information
Terms related to this study
Keywords
Additional Relevant MeSH Terms
Other Study ID Numbers
- Internal-15894
This information was retrieved directly from the website clinicaltrials.gov without any changes. If you have any requests to change, remove or update your study details, please contact register@clinicaltrials.gov. As soon as a change is implemented on clinicaltrials.gov, this will be updated automatically on our website as well.