Ignite Creation Date:
2024-05-11 @ 8:31 AM
Last Modification Date:
2024-10-26 @ 3:29 PM
Study NCT ID:
NCT06410014
Status:
RECRUITING
Last Update Posted:
2024-05-10
First Post:
2024-03-11
Brief Title:
Assessment of Overall Functioning in Patients With Complex Health Issues
Sponsor:
University Hospital Bispebjerg and Frederiksberg
Organization:
University Hospital Bispebjerg and Frederiksberg
Study Overview
Official Title:
Assessment of Overall Functioning in Patients With Complex Health Issues
Status:
RECRUITING
Status Verified Date:
2024-05
Last Known Status:
None
Delayed Posting:
No
If Stopped, Why?:
Not Stopped
Has Expanded Access:
False
If Expanded Access, NCT#:
N/A
Has Expanded Access, NCT# Status:
N/A
Acronym:
CPH-Func
Brief Summary:
The overall aim of the study is to assess whether each outcome measures the same aspect of overall functioning or contributes with different aspects More specifically the aim of this study is to investigate the correlation between each single instrument
During study period all patients presenting at our clinic will be offered to participate in the study Patients will be included in the study when referred to the department of Social Medicine and providing written informed consent to participate in the study Inclusion will continue until 100 patients have completed an AMPS test All participants will apart from standard procedure be asked to complete
An AMPS-test
ADL-Q Questionnaire concerning Activities of Daily Living
ADL-I Interview based questionnaire concerning Activites of Daily Living
As standard procedure all participants will also performcomplete
30 seconds chair stand test 30sCST
Hand grip strength HGS
Evaluation of ambulation Cumulated Ambulation Score CAS
WORQ Work Rehabilitation Questionnaire
To obtain the aim of the study correlation-analysis will be performed to investigate the relationship between each included instruments
During study period all patients presenting at our clinic will be offered to participate in the study Patients will be included in the study when referred to the department of Social Medicine and providing written informed consent to participate in the study Inclusion will continue until 100 patients have completed an AMPS test All participants will apart from standard procedure be asked to complete
An AMPS-test
ADL-Q Questionnaire concerning Activities of Daily Living
ADL-I Interview based questionnaire concerning Activites of Daily Living
As standard procedure all participants will also performcomplete
30 seconds chair stand test 30sCST
Hand grip strength HGS
Evaluation of ambulation Cumulated Ambulation Score CAS
WORQ Work Rehabilitation Questionnaire
To obtain the aim of the study correlation-analysis will be performed to investigate the relationship between each included instruments
Detailed Description:
None
Study Oversight
Has Oversight DMC:
None
Is a FDA Regulated Drug?:
False
Is a FDA Regulated Device?:
False
Is an Unapproved Device?:
None
Is a PPSD?:
None
Is a US Export?:
None
Is an FDA AA801 Violation?:
None