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Physical Activity During Hospitalization and Hospital-Associated Disability

18 de septiembre de 2026 actualizado por: Lea Kromann Etzerodt, Hvidovre University Hospital

Physical Activity as Prevention of Hospital-Associated Disability in Acutely Hospitalized Older Adults - How Much is Enough and What do the Patients Prefer?

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.

Descripción general del estudio

Estado

Aún no reclutando

Condiciones

Intervención / Tratamiento

Descripción detallada

This study is a prospective cohort study investigating physical activity, functioning, and hospital-associated disability (HAD) in acutely hospitalized older adults. The study also examines patients' ability, preferences, motivation, and barriers related to physical activity during hospitalization and after discharge.

Physical activity levels are generally low among older adults during acute hospitalization and are associated with an increased risk of HAD. Physical activity and exercise are recommended as strategies to prevent functional decline during hospitalization. However, there is currently no clear threshold for how much physical activity is needed to reduce the risk of HAD. Furthermore, many acutely hospitalized older adults have limited capacity or motivation to engage in structured exercise, highlighting the need to understand which forms and levels of physical activity are both clinically relevant and feasible from the patients' perspective.

The study will include 170 adults aged 65 years or older who are 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.

During hospitalization:

At inclusion, participants will undergo a baseline assessment consisting of clinical tests and questionnaires assessing functioning, mobility, frailty, health literacy, general health, physical activity, and demographic characteristics.

24-hour physical activity will be objectively measured using SENS motion® sensor technology. The sensor will be worn continuously during hospitalization and will provide information on daily step count and time spent walking, standing, sitting, and lying down. Self-reported mobility during hospitalization will additionally be assessed using the Danish version of the Acute Care Mobility Assessment (ACMA-DK).

During hospitalization participants' imagined and actual ability to perform different forms of physical activity will also be assessed, together with their preferences, motivation, and barriers related to physical activity. Participants will be asked to evaluate and perform two clinically relevant activity types: hallway walking and resistance exercise. They will also be asked about their preference for group-based functional training.

1 week after discharge: Participants will be contacted by telephone to assess functioning and the development of HAD following hospitalization.

4 weeks after discharge: Participants will be contacted by telephone to reassess functioning and whether functional decline following hospitalization persists.

8 weeks after discharge: An 8-week follow-up assessment will be conducted in the participant's home. Physical activity after discharge will be objectively measured using SENS motion® sensor technology for seven consecutive days prior to the 8-week follow-up. At the follow-up visit, physical function, mobility, and the development or persistence of HAD will be assessed.

A qualitative study is embedded within the prospective cohort to explore patients' experiences and perspectives on physical activity after discharge. Participants will be recruited among patients who have completed the 8-week follow-up. Semi-structured interviews will explore motivation, barriers, and preferences related to physical activity after discharge, as well as experiences with rehabilitation.

The overall aim of the project is to integrate objectively measured physical activity patterns, clinical measures of functioning, and patients' own experiences and preferences to contribute to the development of a practice-oriented and patient-centered approach to preventing HAD in acutely hospitalized older adults.

Tipo de estudio

De observación

Inscripción (Estimado)

170

Contactos y Ubicaciones

Esta sección proporciona los datos de contacto de quienes realizan el estudio e información sobre dónde se lleva a cabo este estudio.

Estudio Contacto

Copia de seguridad de contactos de estudio

Ubicaciones de estudio

Criterios de participación

Los investigadores buscan personas que se ajusten a una determinada descripción, denominada criterio de elegibilidad. Algunos ejemplos de estos criterios son el estado de salud general de una persona o tratamientos previos.

Criterio de elegibilidad

Edades elegibles para estudiar

65 años y mayores (Adulto Mayor)

Acepta Voluntarios Saludables

No

Géneros elegibles para el estudio

Todos

Método de muestreo

Muestra de probabilidad

Población de estudio

Older adults (65 years or older) acutely admitted to the Department of Geriatrics or the Department of Cardiology at Copenhagen University Hospital, Hvidovre.

Descripción

Inclusion Criteria:

  • Aged 65 years or older
  • Acutely admitted to the Department of Geriatrics or the Department of Cardiology

Exclusion Criteria:

  • In isolation
  • Delirium
  • Unable to provide informed consent
  • Unable to speak and understand Danish
  • Unable to take one step

Plan de estudios

Esta sección proporciona detalles del plan de estudio, incluido cómo está diseñado el estudio y qué mide el estudio.

¿Cómo está diseñado el estudio?

Detalles de diseño

  • Modelos observacionales: COHORT
  • Perspectivas temporales: PROSPECTIVE

Cohortes e Intervenciones

Grupo / Cohorte
Intervención / Tratamiento
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.

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

¿Qué mide el estudio?

Medidas de resultado primarias

Medida de resultado
Medida Descripción
Periodo de tiempo
Hospital-associated disability
Periodo de tiempo: At inclusion and 1, 4 and 8 weeks after discharge

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
Periodo de tiempo: At inclusion

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
Periodo de tiempo: At inclusion

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
Periodo de tiempo: At inclusion

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

Medidas de resultado secundarias

Medida de resultado
Medida Descripción
Periodo de tiempo
Mean Daily steps
Periodo de tiempo: From inclusion through hospital discharge, an average of 5 days; and 7 consecutive days before the 8-week follow-up

Number of daily steps assessed by a SENS motion® accelerometer worn continuously from inclusion and throughout hospitalization and for seven consecutive days prior to the 8-week follow-up after discharge.

A measurement day is considered valid if more than 20 hours of 24-hour mobility data are available. For each participant, mean daily step count is calculated across all available valid days within each measurement period.

From inclusion through hospital discharge, an average of 5 days; and 7 consecutive days before the 8-week follow-up
Mean daily uptime
Periodo de tiempo: From inclusion through hospital discharge, an average of 5 days; and 7 consecutive days before the 8-week follow-up

Daily time spent in uptime assessed by a SENS motion® accelerometer worn continuously from inclusion and throughout hospitalization and for seven consecutive days prior to the 8-week follow-up after discharge.

A measurement day is considered valid if more than 20 hours of 24-hour mobility data are available. For each participant, mean daily step count is calculated across all available valid days within each measurement period.

From inclusion through hospital discharge, an average of 5 days; and 7 consecutive days before the 8-week follow-up
Mean daily walking
Periodo de tiempo: From inclusion through hospital discharge, an average of 5 days; and 7 consecutive days before the 8-week follow-up

Daily time spent walking assessed by a SENS motion® accelerometer worn continuously from inclusion and throughout hospitalization and for seven consecutive days prior to the 8-week follow-up after discharge.

A measurement day is considered valid if more than 20 hours of 24-hour mobility data are available. For each participant, mean daily step count is calculated across all available valid days within each measurement period.

From inclusion through hospital discharge, an average of 5 days; and 7 consecutive days before the 8-week follow-up
Mean daily standing
Periodo de tiempo: From inclusion through hospital discharge, an average of 5 days; and 7 consecutive days before the 8-week follow-up

Daily time spent standing assessed by a SENS motion® accelerometer worn continuously from inclusion and throughout hospitalization and for seven consecutive days prior to the 8-week follow-up after discharge.

A measurement day is considered valid if more than 20 hours of 24-hour mobility data are available. For each participant, mean daily step count is calculated across all available valid days within each measurement period.

From inclusion through hospital discharge, an average of 5 days; and 7 consecutive days before the 8-week follow-up
Mean daily lying/sitting
Periodo de tiempo: From inclusion through hospital discharge, an average of 5 days; and 7 consecutive days before the 8-week follow-up

Daily time spent sitting or lying assessed by a SENS motion® accelerometer worn continuously from inclusion and throughout hospitalization and for seven consecutive days prior to the 8-week follow-up after discharge.

A measurement day is considered valid if more than 20 hours of 24-hour mobility data are available. For each participant, mean daily step count is calculated across all available valid days within each measurement period.

From inclusion through hospital discharge, an average of 5 days; and 7 consecutive days before the 8-week follow-up

Otras medidas de resultado

Medida de resultado
Medida Descripción
Periodo de tiempo
Self-reported mobility
Periodo de tiempo: Days 2, 4 and 6 after inclusion during hospitalization

Self-reported mobility by the Acute Care Mobility Assessment. A score of 0-12 can be obtained, with 0 reflecting poor mobility and 12 reflecting a high level of mobility.

Days 2, 4 and 6 after inclusion during hospitalization
Life space mobility
Periodo de tiempo: At inclusion and 4 and 8 weeks post discharge

By the Life Space Assessment-DK, which measure mobility and level of dependence in mobility. A score of 0-120 can be obtained, with 0 reflecting poor mobility and 120 reflecting high mobility

At inclusion and 4 and 8 weeks post discharge
Self-reported pre-admission (2 weeks prior to admission) and post discharge mobility
Periodo de tiempo: At inclusion and 1, 4 and 8 weeks post discharge

By the New Mobility Score, which assesses the ability to walk indoors and outdoors and the ability to go shopping. A score from 0-9 can be obtained, with 0 reflecting low mobility and 9 reflecting high mobility.

At inclusion and 1, 4 and 8 weeks post discharge
Frailty pre-admission (2 weeks prior to admission)
Periodo de tiempo: At inclusion

By the Clinical Frailty Scale, which is a clinical evaluation of the degree of frailty of a person. It is scored by health care professionals on a scale from 1 (very fit) to 9 (terminally ill)

At inclusion
Cognitive status
Periodo de tiempo: At inclusion

By the Orientation Memory Concentration Test, which is a screening of cognitive function. A score from 0 to 28 obtained, with lower scores reflecting poorer cognition (0-7: highly impaired; 8-17 points: moderately impaired; 18-24 points: mildly impaired; 25-28 points: no or insignificant impairment).

At inclusion
Basic mobility
Periodo de tiempo: At inclusion, day 2, 4 and 6 after inclusion during hospitalization and 8 weeks post discharge

By the Cummulated Ambulation Score, which assessed the ability of a person to get in and out of bed, sit to stand from a chair and walk. It is scored from 0 to 6 with 0 reflecting inability to perform the 3 activities and a score of 6 reflecting independence in the three activities.

At inclusion, day 2, 4 and 6 after inclusion during hospitalization and 8 weeks post discharge
Gait speed
Periodo de tiempo: At inclusion and 8 weeks post discharge

By the 4-meter gait speed test. It assesses the patient's current gait speed on a 4-meter course. The test is scored in m/s.

At inclusion and 8 weeks post discharge
Readmission
Periodo de tiempo: 6 month post discharge

Number of readmissions within 6 months post discharge

6 month post discharge
Handgrip strength
Periodo de tiempo: At inclusion and 8 weeks post discharge

Handgrip strength of the dominant hand assessed using a handheld dynamometer. Three attempts are performed, and the highest measured value is used for analysis.

At inclusion and 8 weeks post discharge
Lower-extemity muscle strenght
Periodo de tiempo: At inclusion and 8 weeks post discharge

Assessed by Sit-to-stand test, as the number of times the participant can rise from and sit down on a chair during 30 seconds.

At inclusion and 8 weeks post discharge
Concern about falling
Periodo de tiempo: At inclusion and 1, 4 and 8 weeks post discharge

Concern about falling during activities of daily living assessed by the 7-item Short Falls Efficacy Scale (Short FES-I). Each item is scored from 1 to 4, giving a total score from 7 to 28, with higher scores indicating greater concern about falling.

At inclusion and 1, 4 and 8 weeks post discharge

Colaboradores e Investigadores

Aquí es donde encontrará personas y organizaciones involucradas en este estudio.

Patrocinador

Colaboradores

Investigadores

  • Investigador principal: Lea Kromann Etzerodt, MHSc, Department of Clinical Research, Copenhagen University Hospital Hvidovre

Fechas de registro del estudio

Estas fechas rastrean el progreso del registro del estudio y los envíos de resultados resumidos a ClinicalTrials.gov. Los registros del estudio y los resultados informados son revisados ​​por la Biblioteca Nacional de Medicina (NLM) para asegurarse de que cumplan con los estándares de control de calidad específicos antes de publicarlos en el sitio web público.

Fechas importantes del estudio

Inicio del estudio (Estimado)

1 de septiembre de 2026

Finalización primaria (Estimado)

1 de octubre de 2027

Finalización del estudio (Estimado)

1 de mayo de 2029

Fechas de registro del estudio

Enviado por primera vez

9 de septiembre de 2026

Primero enviado que cumplió con los criterios de control de calidad

18 de septiembre de 2026

Publicado por primera vez (Actual)

21 de septiembre de 2026

Actualizaciones de registros de estudio

Última actualización publicada (Actual)

21 de septiembre de 2026

Última actualización enviada que cumplió con los criterios de control de calidad

18 de septiembre de 2026

Última verificación

1 de septiembre de 2026

Más información

Términos relacionados con este estudio

Otros números de identificación del estudio

  • RESTART PhD - VEK (H-26035511)

Plan de datos de participantes individuales (IPD)

¿Planea compartir datos de participantes individuales (IPD)?

NO

Descripción del plan IPD

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.

Información sobre medicamentos y dispositivos, documentos del estudio

Estudia un producto farmacéutico regulado por la FDA de EE. UU.

No

Estudia un producto de dispositivo regulado por la FDA de EE. UU.

No

Esta información se obtuvo directamente del sitio web clinicaltrials.gov sin cambios. Si tiene alguna solicitud para cambiar, eliminar o actualizar los detalles de su estudio, comuníquese con register@clinicaltrials.gov. Tan pronto como se implemente un cambio en clinicaltrials.gov, también se actualizará automáticamente en nuestro sitio web. .