ClinicalTrials.Veeva

Menu

Assessment of Overall Functioning in Patients With Complex Health Issues (CPH-Func)

U

University Hospital Bispebjerg and Frederiksberg

Status

Enrolling

Conditions

Disability Evaluation
Muscle Strength
Health Status
ADL Motor Skills
Activities of Daily Living
Surveys and Questionnaires
Physical Examination

Treatments

Other: No intervention is performed

Study type

Observational

Funder types

Other

Identifiers

NCT06410014
H23030964

Details and patient eligibility

About

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 perform/complete:

  • 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.

Enrollment

100 estimated patients

Sex

All

Ages

18+ years old

Volunteers

No Healthy Volunteers

Inclusion criteria

  • All patients referred by a municipality to the Department of Social Medicine at Bispebjerg and Frederiksberg Hospital for a clinical assessment (Klinisk Funktion) who provide written consent to participate.

Exclusion criteria

  • Insufficient ability to communicate either in written or oral Danish

Trial design

100 participants in 1 patient group

Participating patients
Description:
All patient who have consented to participate in the study
Treatment:
Other: No intervention is performed

Trial documents
1

Trial contacts and locations

1

Loading...

Central trial contact

Poul Frost, M.D. Ph.D.; Anna Karnøe Knudsen, M.D.

Data sourced from clinicaltrials.gov

Clinical trials

Find clinical trialsTrials by location
© Copyright 2026 Veeva Systems