Physical Activity During Hospitalization and Hospital-Associated Disability
Physical Activity as Prevention of Hospital-Associated Disability in Acutely Hospitalized Older Adults - How Much is Enough and What do the Patients Prefer?
1 other identifier
observational
170
1 country
1
Brief Summary
This study examines physical activity during and after hospitalization in acutely hospitalized older adults and its association with hospital-associated disability (HAD). Older adults have low levels of physical activity during acute hospitalization, which is associated with an increased risk of HAD. HAD is a decline in the ability to perform activities of daily living that occurs in relation to hospitalization and cannot be explained by the acute illness alone. HAD affects up to 30% of acutely hospitalized older adults and is associated with adverse outcomes, including an increased risk of discharge to a nursing home, readmission, and mortality. Furthermore, patients who develop HAD are at risk of not regaining their pre-admission functional level and experiencing persistent functional decline after discharge. Physical activity and exercise are recommended as strategies to prevent HAD. However, many acutely hospitalized older adults have limited capacity or motivation to engage in structured exercise. It therefore remains unclear how much physical activity during hospitalization is sufficient to reduce the risk of HAD and which types of physical activity patients are able and prefer to perform. The study will also examine patients' ability and preferences for different types of physical activity during hospitalization and explore their motivation, barriers, and preferences for physical activity after discharge. The results may help identify clinically relevant levels of physical activity during hospitalization and contribute to more patient-centered approaches to supporting physical activity and preventing functional decline during and after hospitalization.
Trial Health
Trial Health Score
Automated assessment based on enrollment pace, timeline, and geographic reach
participants targeted
Target at P50-P75 for all trials
Started Sep 2026
Typical duration for all trials
1 active site
Health score is calculated from publicly available data and should be used for screening purposes only.
Trial Relationships
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Study Timeline
Key milestones and dates
Study Start
First participant enrolled
September 1, 2026
CompletedFirst Submitted
Initial submission to the registry
September 9, 2026
CompletedFirst Posted
Study publicly available on registry
September 21, 2026
CompletedPrimary Completion
Last participant's last visit for primary outcome
October 1, 2027
ExpectedStudy Completion
Last participant's last visit for all outcomes
May 1, 2029
September 21, 2026
September 1, 2026
1.1 years
September 9, 2026
September 18, 2026
Conditions
Keywords
Outcome Measures
Primary Outcomes (4)
Hospital-associated disability
Hospital-associated disability (HAD) is defined as a new decline in functional independence in at least one activity compared with the participant's pre-admission level. Functional independence is assessed using three components: six basic activities of daily living from the Katz Index (bathing, dressing, toileting, transferring, continence, and feeding); five instrumental activities of daily living inspired by the Lawton IADL Index (shopping, housekeeping, laundry, food preparation, and medication management); and four mobility-related activities (walking 400 meters without rest, climbing or descending one flight of stairs without rest, carrying 5 kg, and driving a car). Each activity is scored as unable to perform (0), able to perform with assistance (1), or able to perform independently (2). Participants with a decline in independence in at least one activity compared with their retrospectively assessed pre-admission level are classified as having HAD.
At inclusion and 1, 4 and 8 weeks after discharge
Imagined ability to perform physical activity during hospitalization
Participants' imagined ability to perform physical activity during hospitalization will be assessed by asking whether they can imagine performing the activity daily during hospitalization. Imagined ability will be assessed for hallway walking (200 steps) and resistance exercise (three sets of 8-12 sit-to-stand repetitions) and group-based functionel training.
At inclusion
Actual ability to perform physical activity during hospitalization
Participants' actual ability to perform physical activity during hospitalization will be assessed by asking them to perform hallway walking (200 steps) and resistance exercise (three sets of 8-12 sit-to-stand repetitions). For each activity, actual ability will be categorized as able to complete the activity as defined, 0) unable to complete the activity, 1) able to complete the activity with assistance and 2) able to complete the activity independently. Reasons for inability to complete an activity will be recorded.
At inclusion
Preferred type of physical activity during hospitalization
Participants will be asked which type of physical activity they prefer: hallway walking, resistance training and group-based functional training. (Group-based functional training will be assessed as a preference only and will not be physically performed as part of the assessment).
At inclusion
Secondary Outcomes (5)
Mean Daily steps
From inclusion through hospital discharge, an average of 5 days; and 7 consecutive days before the 8-week follow-up
Mean daily uptime
From inclusion through hospital discharge, an average of 5 days; and 7 consecutive days before the 8-week follow-up
Mean daily walking
From inclusion through hospital discharge, an average of 5 days; and 7 consecutive days before the 8-week follow-up
Mean daily standing
From inclusion through hospital discharge, an average of 5 days; and 7 consecutive days before the 8-week follow-up
Mean daily lying/sitting
From inclusion through hospital discharge, an average of 5 days; and 7 consecutive days before the 8-week follow-up
Other Outcomes (11)
Self-reported mobility
Days 2, 4 and 6 after inclusion during hospitalization
Life space mobility
At inclusion and 4 and 8 weeks post discharge
Self-reported pre-admission (2 weeks prior to admission) and post discharge mobility
At inclusion and 1, 4 and 8 weeks post discharge
- +8 more other outcomes
Study Arms (1)
Acutely Hospitalized Older Adults
A prospective cohort of 170 adults aged 65 years or older acutely admitted to the Department of Geriatrics or the Department of Cardiology at Copenhagen University Hospital - Hvidovre. Participants will be consecutively recruited within 48 hours of admission and followed during hospitalization and at 1, 4, and 8 weeks after discharge.
Interventions
Participants will receive standard care throughout hospitalization. In addition to standard care, participants will take part in a single supervised assessment of their ability and preferences for different types of physical activity. The assessment includes hallway walking (200 steps, with walking aids or assistance if needed) and resistance exercise consisting of three sets of 8-12 repetition maximum sit-to-stands. Participants will also be asked about their preference for group-based functional training and about their motivation and barriers related to physical activity. Physical activity will be objectively measured using SENS motion® sensor technology continuously during hospitalization and for seven consecutive days prior to the 8-week follow-up after discharge. Self-reported mobility during hospitalization will also be assessed. After discharge, participants' experiences, motivation, barriers, and preferences related to physical activity and rehabilitation will be explored th
Eligibility Criteria
Older adults (65 years or older) acutely admitted to the Department of Geriatrics or the Department of Cardiology at Copenhagen University Hospital, Hvidovre.
You may qualify if:
- Aged 65 years or older
- Acutely admitted to the Department of Geriatrics or the Department of Cardiology
You may not qualify if:
- In isolation
- Delirium
- Unable to provide informed consent
- Unable to speak and understand Danish
- Unable to take one step
Contact the study team to confirm eligibility.
Sponsors & Collaborators
Study Sites (1)
Copenhagen University Hospital, Hvidovre
Hvidovre, Denmark
MeSH Terms
Conditions
Condition Hierarchy (Ancestors)
Study Officials
- PRINCIPAL INVESTIGATOR
Lea Kromann Etzerodt, MHSc
Department of Clinical Research, Copenhagen University Hospital Hvidovre
Central Study Contacts
Study Design
- Study Type
- observational
- Observational Model
- COHORT
- Time Perspective
- PROSPECTIVE
- Sponsor Type
- OTHER
- Responsible Party
- PRINCIPAL INVESTIGATOR
- PI Title
- Principal Investigator (PhD scientist)
Study Record Dates
First Submitted
September 9, 2026
First Posted
September 21, 2026
Study Start
September 1, 2026
Primary Completion (Estimated)
October 1, 2027
Study Completion (Estimated)
May 1, 2029
Last Updated
September 21, 2026
Record last verified: 2026-09
Data Sharing
- IPD Sharing
- Will not share
Due to Danish data protection legislation, individual participant data cannot be publicly shared. Access to pseudonymized data may be granted upon reasonable request and approval by the Danish Data Protection Agency.