Skip to content

Assessment of Overall Functioning in Patients With Complex Health Issues

Assessment of Overall Functioning in Patients With Complex Health Issues

Status
Recruiting
Phases
Unknown
Study type
Observational
Source
ClinicalTrials.gov
Registry ID
NCT06410014
Acronym
CPH-Func
Enrollment
100
Registered
2024-05-10
Start date
2023-10-10
Completion date
2025-02-01
Last updated
2024-12-09

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

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

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 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

The study is observational

Sponsors

University Hospital Bispebjerg and Frederiksberg
Lead SponsorOTHER

Study design

Observational model
COHORT
Time perspective
CROSS_SECTIONAL

Eligibility

Sex/Gender
ALL
Age
18 Years to No maximum
Healthy volunteers
No

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

Design outcomes

Primary

MeasureTime frameDescription
Assessment of Motor and Process Skills (AMPS)Within 21 days from baselineBased on observation of 2 ADL tasks the quality of 16 motor and 20 process skills are scored on a four-point ordinal scale. Using Rasch analysis the raw ordinal scores are converted into two overall ADL ability measures, representing ADL motor and ADL process ability expressed in logits.

Secondary

MeasureTime frameDescription
Hand Grip strengthBaselineMeasured in kilograms
Cumulated Ambulation Score (CAS)BaselineScoring of three mobility activities on a three point ordinal scale (zero to 2). The scores are summed resulting in a total score ranging from 0 to 6.
30 seconds chair stand testBaselineTotal number of stands performed in 30 seconds
ADL-QWithin 21 days from baselineRaw data collected in the questionnaire is scored on a four-point ordinal scale and subsequently converted into a linear measure of self-reported ADL ability expressed in logits (log-odds probability units).
Work Rehabilitation Questionnaire (WORQ)The questionnaire is responded one time during a periode ranging from 7 days prior to baseline until 21 days after baselineThe questionnaire consists of 17 items on sociodemographic topics and 40 items related to overall functioning. The 40 items are each scored on a response scale ranging from 0 to 10. The results are summed in four linear subscales addressing emotion, cognition, dexterity and mobility. A total sum score is performed.
ADL-IWithin 21 days from baselineRaw data collected in the interview is scored on a four-point ordinal scale and subsequently converted into a linear measure of self-reported ADL ability expressed in logits (log-odds probability units).

Countries

Denmark

Contacts

Primary ContactAnna Karnøe Knudsen, M.D.
anna.karnoee.knudsen@regionh.dk+4521744720
Backup ContactPoul Frost, M.D. Ph.D.
poul.frost@regionh.dk+45 38 64 98 00

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 4, 2026