Assessment of Overall Functioning in Patients With Complex Health Issues
For patients and families
In plain language
An automatic summary of structured registry data. It is an orientation aid, not a substitute for the official protocol or a physician assessment.
- What is being studied
- The protocol lists: No intervention is performed.
- Who it may be relevant to
- Registry conditions: Activities of Daily Living, Surveys and Questionnaires, ADL Motor Skills, Disability Evaluation. Basic parameters: from 18 years · All.
- What needs checking
- Age, condition and sex are only basic indicators. Prior treatment, laboratory values and other mandatory requirements appear in the eligibility criteria below.
- Where it takes place
- Denmark
- Next step
- Save the trial, show it to the treating physician, and confirm current recruitment with the study center. Costs, documents and travel →
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Overview
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.
Interventions
- Other No intervention is performed
The study is observational
Primary outcome measures
- Assessment of Motor and Process Skills (AMPS) [Time frame: Within 21 days from baseline]
Secondary outcome measures (6)
- 30 seconds chair stand test [Time frame: Baseline]
- Hand Grip strength [Time frame: Baseline]
- Cumulated Ambulation Score (CAS) [Time frame: Baseline]
- ADL-I [Time frame: Within 21 days from baseline]
- ADL-Q [Time frame: Within 21 days from baseline]
- Work Rehabilitation Questionnaire (WORQ) [Time frame: The questionnaire is responded one time during a periode ranging from 7 days prior to baseline until 21 days after baseline]
Eligibility criteria
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
Criteria are shown verbatim from the registry (in English). Final eligibility is always assessed by the study center.
Healthy volunteers: No
Study design
- Observational model
- Cohort
Study locations
Denmark · 1 center
- Afdeling for Socialmedicin — Frederiksberg
Identifiers
NCT: NCT06410014 · H23030964