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The WALK-Copenhagen Trial (WALK-Cph): a Mixed Methods Study

WALK-Copenhagen (WALK-Cph): Promoting Physical Activity in Older Adults During Hospitalization and After Discharge

Status
Terminated
Phases
NA
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT03825497
Enrollment
18
Registered
2019-01-31
Start date
2018-09-25
Completion date
2019-10-31
Last updated
2019-11-22

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

Conditions

Activity, Hospitalization

Keywords

older medical patient, mobility, hospitalization, activity monitoring, cross sectoral

Brief summary

The WALK-Copenhagen project aims at enhancing physical activity during and after hospitalization in older medical patients by an intervention developed in co-operation with key stakeholders

Detailed description

In four phases we will develop (Phase 1), fidelity- and feasibility test (Phase 2), efficacy test (Phase 3) and adoption test the intervention (Phase 4). The project will use a combination of qualitative (Phase 1-4) and quantitative methods (Phase 2-3) and consists of two parallel tracks - WALK-Intervention and WALK-Implementation. Phase 1 of the study has been completed. Through workshops with patients, relatives, health professionals and researchers we have developped an intervention to enhance physical activity. Phase 2 will be carried out in October 2018 and January 2019 at Copenhagen University Hospital Hvidovre and in February 2019 at Copenhagen University Hospital, Frederiksberg. The developed intervention will be fidelity tested through daily observations at the wards. Also, the intervention will be feasibility tested in a prospective cohort study aiming at qualifying the intervention, testing recruitment strategies, testing patient willingness towards the intervention, testing randomization and blinding procedures and estimating an inclusion rate for Phase 3 (randomized controlled trial) to be conducted in 2019. Update March 2019: Due to a political decision to close down the medical ward at Copenhagen University Hospital, Frederiksberg in the spring of 2019, it was decided to change Phase 3 to a cohort study at Copenhagen University Hospital, Hvidovre. This decision was based on the fact that the methodological setup of the study (cluster RCT) was unintentionally changed due to the close down of one of the intervention wards. Update November 2019: Due to changes in characteristics of patients admitted to the intervention ward and thus a very slow inclusion rate in Phase 3 (Cohort Study), it was decided to terminate inclusion of patients. Qualitative data will still be collected as anticipated.

Interventions

OTHERPromotion of activity during and after hospitalization

1\) a welcome folder encouraging physical activity; 2) encouragement to use a walk path established in the ward; 3) encouragement to use posters containing exercise suggestions;4) prescription of a walk-plan for in-hospital use; 5) encouragement to pick up clothes and beverages by oneself; 6) prescription of a walk-plan at discharge for at home use 7) follow-up on walk plan after discharge by municipality

Sponsors

Velux Fonden
CollaboratorOTHER
Danske Fysioterapeuter
CollaboratorOTHER
Copenhagen University Hospital, Hvidovre
Lead SponsorOTHER

Study design

Allocation
RANDOMIZED
Intervention model
PARALLEL
Primary purpose
TREATMENT
Masking
NONE

Masking description

All patients at the intervention wards will receive the intervention why neither investigators nor outcome assessors will be blinded to the intervention. Patients at intervention and control wards will get equal information regarding the study and will be asked to participate in equal assessments

Intervention model description

A feasibility study at Medical Wards (intervention wards) in Oct 2018, January 2019 and February 2019 prior to a cluster randomized trial. Medical wards at 4 different hospitals representing clusters - 2 intervention clusters and 2 control clusters.

Eligibility

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

Inclusion criteria

* +65 years * acutely admitted to intervention wards * able to walk independently with or without walking aid

Exclusion criteria

* in isolation * inability to cooperate * not able to speak or understand Danish * in treatment for cancer * terminally ill * transferred to intensive care unit or another ward within 24 hours after admission

Design outcomes

Primary

MeasureTime frameDescription
Upright time measured by an ActivPal (PAL Technologies Ltd) activity monitorMean number of hours per day spent upright during hospitalization (up to 7 days)Between group difference in time spent standing or walking per day (Upright time)

Secondary

MeasureTime frameDescription
Time spent lying/sitting measured by an ActivPal (PAL Technologies Ltd) activity monitorMean number of hours per day spent lying/sitting during hospitalization (up to 7 days)Between group difference time spent lying/sitting per day
Change in upright time measured by an ActivPal (PAL Technologies Ltd) activity monitorChange in mean number of hours per day spent upright between hospitalization and 4 weeks after dischargeBetween group difference in change in time spent standing or walking per day (Upright time)
Change in number of steps measured by an ActivPal (PAL Technologies Ltd)activity monitorChange in mean number of steps per day between hospitalization and 4 weeks after dischargebetween group difference in change in number of steps per day
Number of steps measured by an ActivPal (PAL Technologies Ltd) activity monitorMean number of steps per day during hospitalization (up to 7 days)Between group difference in number of steps per day
Change in Life-Space mobility using The University of Alabama at Birmingham (UAB) Life Space Assessment (a 0-120 point scale with 0 representing low mobility and 120 high mobility)Change in Life Space between admission and 4 weeks after dischargeBetween group difference in change in Life Space
Change in 4-meter gait speed testChange in habitual gait speed between admission and 4 weeks after dischargeBetween group in change in Habitual gait speed
Change in mobility using The de Morton Mobility Index (DEMMI) (0-100 point scale with 0 representing low mobility and 100 representing high mobility)Change in DEMMI score between admission and 4 weeks after dischargeBetween group difference in change in mobility
Change in time spent lying/sitting measured by an ActivPal (PAL Technologies Ltd) activity monitorChange in mean number of hours per day spent lying/sitting between hospitalization and 4 weeks after dischargeBetween group difference in change in time spent lying/sitting per day

Countries

Denmark

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 18, 2026