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Monitoring Physical Activity in Acutely Hospitalized Elderly of 70 Years and Older (MPA)

29. september 2020 oppdatert av: Maastricht University Medical Center
This study aims to create reference values regarding the amount of physical activity of acutely hospitalized elderly ≥70 years during hospitalization and aims to create a prediction model in order predict the probability of low amounts of physical activity of acutely hospitalized elderly ≥70 years during hospitalization.

Studieoversikt

Status

Fullført

Detaljert beskrivelse

Rationale: Despite numerous studies supporting adverse outcomes associated with low physical activity (PA), there is insufficient insight in the amount of PA of acutely hospitalized Dutch elderly ≥ 70 years. PA can be objectively measured by accelerometers, but it is time consuming and expensive to provide every patient with an accelerometer. We need to be able to predict which elderly patients are likely to spend low amounts of physical activity during hospitalization. Because of the association between PA and functional decline it is expected that functional assessment tests like the Short Physical Performance Battery (SPPB) or Activity Measure for Post-Acute Care (AM-PAC) could be used as a screening tool to determine which patients will be at risk of low amounts of PA.

Objective: The primary objectives of this study are: 1) To assess the amount of PA of acutely hospitalized elderly ≥70 years during hospitalization and to create reference values regarding the amount of time patients are standing and walking per day and the number of breaks in sedentary time (BST) per day. 2) To be able to predict the probability of low amounts of physical activity during hospitalization for acutely hospitalized elderly ≥70 years.

Study design: This is a single center, observational, prospective cohort study.

Study population: 165 patients aged ≥70 years that are acutely hospitalized at the department of internal and geriatric medicine in the Maastricht University Medical Center (MUMC+).

Method: PA will be monitored with an accelerometer from inclusion (t0) until the day of intended discharge (t1). A functional assessment (SPPB and AM-PAC) will be performed at t0. Medical and demographic data will be obtained from the medical record and by patient report.

Main study parameters/endpoints: Mean number of minutes spent physically active (standing and walking) per day, dichotomized into a low and high amount of time spent physically active per day during hospitalization for the prediction model. Mean number of BST per day, dichotomized into a low and high number of BST per day during hospitalization for the prediction model.

Studietype

Observasjonsmessig

Registrering (Faktiske)

165

Kontakter og plasseringer

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Studiesteder

    • Limburg
      • Maastricht, Limburg, Nederland, 6229 HX
        • MaastrichtUMC

Deltakelseskriterier

Forskere ser etter personer som passer til en bestemt beskrivelse, kalt kvalifikasjonskriterier. Noen eksempler på disse kriteriene er en persons generelle helsetilstand eller tidligere behandlinger.

Kvalifikasjonskriterier

Alder som er kvalifisert for studier

70 år og eldre (Eldre voksen)

Tar imot friske frivillige

Nei

Kjønn som er kvalifisert for studier

Alle

Prøvetakingsmetode

Sannsynlighetsprøve

Studiepopulasjon

Patients aged ≥70 years that are acutely hospitalized in MUMC+ at the department of Internal and Geriatric Medicine.

Beskrivelse

Inclusion Criteria:

  • 70 years or older
  • Acutely hospitalized in MUMC+ at the department of Internal and Geriatric Medicine
  • Sufficient understanding of the Dutch language
  • Living at home before hospitalization
  • Able to walk independently 2 weeks before admission, as scored on the Functional Ambulation Categories (FAC >3)

Exclusion Criteria:

  • A life expectancy of less than three months as assessed by the attending physician
  • Incapacitated subjects
  • The inability to follow instructions due to cognitive problems or severe agitation
  • A contraindication to wearing an accelerometer, fixated by a hypoallergenic plaster, on the upper leg (such as active bilateral upper leg infection, severe edema or bilateral transfemoral amputation)
  • (Re)admittance to the intensive care unit
  • Presence of contraindications to walking as assessed by the attending physician
  • Previous participation to this study

Studieplan

Denne delen gir detaljer om studieplanen, inkludert hvordan studien er utformet og hva studien måler.

Hvordan er studiet utformet?

Designdetaljer

Hva måler studien?

Primære resultatmål

Resultatmål
Tiltaksbeskrivelse
Tidsramme
Mean number of minutes spent physically active (standing and walking) per day
Tidsramme: Measured continuously from the day of inclusion (Day 0) until the day the subject is medically ready to be discharged from the hospital.
Defined as the total number of minutes standing and walking divided by the total number of valid measurement days in the period between inclusion and (intended) discharge. In order to create a prediction model, this will be dichotomized into a low and high amount of time spent physically active per day during hospitalization. As the estimated event rate of a high amount of time spent physically active per day during hospitalization is 50%, the cut-off value between a low and high amount of time spent physically active will be defined by dividing the cohort at the median.
Measured continuously from the day of inclusion (Day 0) until the day the subject is medically ready to be discharged from the hospital.
Mean number of breaks in sedentary time (BST) per day
Tidsramme: Measured continuously from the day of inclusion (Day 0) until the day the subject is medically ready to be discharged from the hospital.

Defined as the total number of BST divided by the total number of valid measurement days in the period between inclusion and (intended) discharge. A BST is defined as any transition from being sedentary (lying or sitting) to being physically active (standing or walking).

In order to create a prediction model, this will be dichotomized into a low and high number of breaks in sedentary time per day during hospitalization. As the estimated event rate of a high number of breaks in sedentary time per day during hospitalization is 50%, the cut-off value between a low and high number of breaks in sedentary time will be defined by dividing the cohort at the median.

Measured continuously from the day of inclusion (Day 0) until the day the subject is medically ready to be discharged from the hospital.

Sekundære resultatmål

Resultatmål
Tiltaksbeskrivelse
Tidsramme
Short Physical Performance Battery scores (summary and component scores)
Tidsramme: Measured on the day of inclusion (Day 0)
Summary score on the scale: 0-12 points. Higher scores indicates better functioning. SPPB evaluates balance, gait, strength and endurance by examining an individual's ability to stand with feet together in side-by-side, semi-tandem and tandem positions, time to walk 4 meter and time to rise from a chair and return to the seated position five times. Component scores (0-4) for the three categories are measured as well.
Measured on the day of inclusion (Day 0)
Activity Measure for Post-Acute Care (AM-PAC) Inpatient Basic Mobility short form score
Tidsramme: Measured on the day of inclusion (Day 0)
The AM-PAC and provides a transparent measure of patients' capabilities in functional mobility during hospitalization. It measures the following daily activities: turning in bed, sitting down and standing up, moving from lying to sitting position, moving from a bed to a chair, walking and climbing stairs (6-24 points).
Measured on the day of inclusion (Day 0)
Age
Tidsramme: Scored once on the day of inclusion (Day 0)
Categories 70-79, 80-89, ≥90 years
Scored once on the day of inclusion (Day 0)
Sex
Tidsramme: Scored once on the day of inclusion (Day 0).
Male / Female
Scored once on the day of inclusion (Day 0).
Disability in activities of daily living (ADLs) two weeks prior to admission
Tidsramme: Scored once the day of inclusion (Day 0).
Number of disabilities on the Katz Index of Independence in Activities of Daily Living (Katz ADL). The Katz ADL measures the patient's ability to perform ADL independently. It is a dichotomous rating (dependant / independent) of six ADL functions, bathing, dressing, toileting, transferring, continence and feeding. It rates the level of independence or dependence in these tasks and is categorized by the amount of assistance needed to complete the task. The researcher will ask the patient how much assistance was needed to complete the tasks 2 weeks prior to admission.
Scored once the day of inclusion (Day 0).
The use of ambulation assistive devices prior to admission
Tidsramme: Scored on the day of inclusion (Day 0).
Yes/No. If yes, specify type of walking aid used prior to admission. The use of ambulation assistive device prior to admission is asked by the researcher.
Scored on the day of inclusion (Day 0).
Clinical diagnosis
Tidsramme: On day of intended discharge from hospital, estimated up to 1 month. (Intended discharge is defined as the day the patient is medically ready for discharge and is either discharged or staying for non-medical reasons.)
Clinical diagnosis as reported in the electronic medical record by the physician. The last reported clinical diagnoses by the physician before intended discharge will be extracted.
On day of intended discharge from hospital, estimated up to 1 month. (Intended discharge is defined as the day the patient is medically ready for discharge and is either discharged or staying for non-medical reasons.)
Physiotherapy consulted during hospitalization
Tidsramme: On day of intended discharge from hospital, estimated up to 1 month. (Intended discharge is defined as the day the patient is medically ready for discharge and is either discharged or staying for non-medical reasons.)
Did the patient receive one or more sessions of physiotherapy between inclusion and intended discharge? (Yes / No). All sessions will be reported by the physical therapist in the electronic medical record.
On day of intended discharge from hospital, estimated up to 1 month. (Intended discharge is defined as the day the patient is medically ready for discharge and is either discharged or staying for non-medical reasons.)

Andre resultatmål

Resultatmål
Tiltaksbeskrivelse
Tidsramme
History of falls in the past six months
Tidsramme: Once, on the day of inclusion (Day 0)
The number of falls in the last 6 months before hospital admission. Measured retrospectively by asking the patient the following question: Have you fallen once or more in the past six months? If yes, how many times? Question is asked by the researcher.
Once, on the day of inclusion (Day 0)
Medical comorbidities
Tidsramme: On day of intended discharge from hospital, estimated up to 1 month. (Intended discharge is defined as the day the patient is medically ready for discharge and is either discharged or staying for non-medical reasons.)
Charlson Comorbidity Index (CCI). Comorbidities are reported by the physician in the electronic medical record. All comorbidities present in the period between admission and intended discharge are extracted by the researcher and used to calculate the Charlson Comorbidity Index.
On day of intended discharge from hospital, estimated up to 1 month. (Intended discharge is defined as the day the patient is medically ready for discharge and is either discharged or staying for non-medical reasons.)
Length of stay
Tidsramme: On day of intended discharge from hospital, estimated up to 1 month. (Intended discharge is defined as the day the patient is medically ready for discharge and is either discharged or staying for non-medical reasons.)
Number of days from admission to the hospital to intended discharge (Defined as the day the patient is medically ready for discharge and is either discharged or staying for non-medical reasons.). Length of stay is retrieved from the electronic medical record.
On day of intended discharge from hospital, estimated up to 1 month. (Intended discharge is defined as the day the patient is medically ready for discharge and is either discharged or staying for non-medical reasons.)
Discharge location
Tidsramme: On day of intended discharge from hospital, estimated up to 1 month. (Intended discharge is defined as the day the patient is medically ready for discharge and is either discharged or staying for non-medical reasons.)
Home, geriatric rehabilitation center, nursing home, other. As reported in the electronic medical record by the physician.
On day of intended discharge from hospital, estimated up to 1 month. (Intended discharge is defined as the day the patient is medically ready for discharge and is either discharged or staying for non-medical reasons.)

Samarbeidspartnere og etterforskere

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Etterforskere

  • Hovedetterforsker: Antoine F Lenssen, Prof., PhD, Maastricht University Medical Center

Publikasjoner og nyttige lenker

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Studierekorddatoer

Disse datoene sporer fremdriften for innsending av studieposter og sammendragsresultater til ClinicalTrials.gov. Studieposter og rapporterte resultater gjennomgås av National Library of Medicine (NLM) for å sikre at de oppfyller spesifikke kvalitetskontrollstandarder før de legges ut på det offentlige nettstedet.

Studer hoveddatoer

Studiestart (Faktiske)

19. oktober 2018

Primær fullføring (Faktiske)

23. mars 2019

Studiet fullført (Faktiske)

23. mars 2020

Datoer for studieregistrering

Først innsendt

14. januar 2019

Først innsendt som oppfylte QC-kriteriene

24. mai 2019

Først lagt ut (Faktiske)

28. mai 2019

Oppdateringer av studieposter

Sist oppdatering lagt ut (Faktiske)

30. september 2020

Siste oppdatering sendt inn som oppfylte QC-kriteriene

29. september 2020

Sist bekreftet

1. september 2020

Mer informasjon

Begreper knyttet til denne studien

Andre studie-ID-numre

  • NL65097.068.18

Plan for individuelle deltakerdata (IPD)

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Studerer et amerikansk FDA-regulert enhetsprodukt

Nei

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