Preventing Hospital Associated Disability in Older Patients: Individualized Nutrition and Exercise Strategy
PrevHAD RCT
2 other identifiers
interventional
360
1 country
1
Brief Summary
Aproximately a third of persons older than 70 years lose physical function and ability to take care of themselves during a stay at a hospital. This is associated to an increased risk of readmission and mortality. Earlier research has shown that insufficient nutrition and physical activity during hospital stay, leading to a loss in muscle mass and strength, plays an important role in this fall in functionality. This study aims to examine if a structured and supervised resistance and mobility exercise intervention, can prevent this fall in functional ability during hospital stay among older patients. The Impact of nutritional status will be investigated by registrering caloric, protein and hydtrational intake during the study period.
Trial Health
Trial Health Score
Automated assessment based on enrollment pace, timeline, and geographic reach
participants targeted
Target at P75+ for not_applicable
Started Feb 2026
Typical duration for not_applicable
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
First Submitted
Initial submission to the registry
January 20, 2026
CompletedFirst Posted
Study publicly available on registry
January 28, 2026
CompletedStudy Start
First participant enrolled
February 3, 2026
CompletedPrimary Completion
Last participant's last visit for primary outcome
February 28, 2027
ExpectedStudy Completion
Last participant's last visit for all outcomes
February 29, 2028
January 30, 2026
January 1, 2026
1.1 years
January 20, 2026
January 28, 2026
Conditions
Keywords
Outcome Measures
Primary Outcomes (1)
Changes in activities of daily living (ADL) function, by Barthel index-100
describes the level of independence in activities of daily living, score of 0 equals total dependence and a score of 100 equals total independence
From enrollment to discharge/transfer from the geriatric care unit (aproximately 5 days), measured again 1 month after discharge.
Secondary Outcomes (14)
Changes in mobility by Cumulated Ambulation Score
From enrollment to discharge/transfer from the geriatric care unit (aproximately 5 days), measured again 1 month after discharge
Changes in Knee extension strength,
From enrollment to discharge/transfer from the geriatric care unit (aproximately 5 days), measured again 1 month after discharge.
Changes in Hand Grip Strength
From enrollment to discharge/transfer from the geriatric care unit (aproximately 5 days), measured again 1 month after discharge.
Changes in Sit-to-stand performance
From enrollment to discharge/transfer from the geriatric care unit (aproximately 5 days), measured again 1 month after discharge.
Changes in Gait speed
From enrollment to discharge/transfer from the geriatric care unit (aproximately 5 days), measured again 1 month after discharge.
- +9 more secondary outcomes
Study Arms (2)
Control
NO INTERVENTIONThe control group will recieve usual care at the geriatric care unit, with mobility exercise performed based on individual preferences and ability, performed by regular care personelle and regular physiotherapy staff.
Exercise intervention
EXPERIMENTALThe exercise intervention group will recieve two times 30 minutes of supervised exercise (mobility and resistance exercise) every day during their stay at the geriatrich care unit.
Interventions
The participants in the intervention group will recieve supervised exercise two times 30 minutes each day during hospitalization. The first exercise pass consists of resistance exercise, and can be performed supine in bed, sitting on the edge of the bed, and in a close-by exercise area, based on participants mobility level. The second exercise pass consists of mobility exercise, aiming to transfer the participant from supine in the bed to sitting position, transfer to chair, walking with or without walking aids or walking on stairs.
Eligibility Criteria
You may qualify if:
- Hospitalized at the geriatric ward
- Speak Danish or English
- Ability to give informed consent
You may not qualify if:
- Moderate to severe Dementia
- Manifest delirium
Contact the study team to confirm eligibility.
Sponsors & Collaborators
Study Sites (1)
Bispebjerg Hospital
Copenhagen, Capital Region, 2400, Denmark
MeSH Terms
Conditions
Interventions
Condition Hierarchy (Ancestors)
Intervention Hierarchy (Ancestors)
Study Officials
- PRINCIPAL INVESTIGATOR
Charlotte Suetta, Professor
Geriatric research unit, Bispebjerg hospital, Copenhagen
Central Study Contacts
Study Design
- Study Type
- interventional
- Phase
- not applicable
- Allocation
- RANDOMIZED
- Masking
- NONE
- Masking Details
- Outcomes at discharge will be measured by a different investigator than at baseline, to mask the baseline measures.
- Purpose
- PREVENTION
- Intervention Model
- PARALLEL
- Sponsor Type
- OTHER
- Responsible Party
- PRINCIPAL INVESTIGATOR
- PI Title
- Professor
Study Record Dates
First Submitted
January 20, 2026
First Posted
January 28, 2026
Study Start
February 3, 2026
Primary Completion (Estimated)
February 28, 2027
Study Completion (Estimated)
February 29, 2028
Last Updated
January 30, 2026
Record last verified: 2026-01
Data Sharing
- IPD Sharing
- Will share
- Shared Documents
- STUDY PROTOCOL, SAP
- Time Frame
- When the main study is published, estimated 1. march 2028, with no end date
- Access Criteria
- Data repository, URL link within the published study
We will share the protocol for the exercise intervention, as well as participants charecteristics and outcome data, in a data repository, when the data can be fully anonymized