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Physical functioning, fatigability, and their relation with recovery in acutely hospitalized older medical patients

Physical functioning, fatigability, and their relation with recovery in acutely hospitalized older medical patients - SeniorLines - 2.0

Status
Recruiting
Phases
Unknown
Study type
Observational
Source
NL-OMON
Registry ID
NL-OMON48844
Enrollment
200
Registered
2018-03-06
Start date
2018-04-01
Completion date
Unknown
Last updated
2024-04-15

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

Conditions

kwetsbaarheid, veroudering fatigability fatigue

Interventions

None listed

Sponsors

centrum voor ouderengeneeskunde
Lead Sponsor

Eligibility

Age
18 Years to 99 Years

Inclusion criteria

Inclusion criteria: aged 70 years or older; willing to participate medically able to participate providing informed consent.

Exclusion criteria

Exclusion criteria: 1. no understanding of the Dutch language; 2. lack of decision making capacity, due to: a.previously diagnosed dementia; b. delirium or other conditions that influence decision making capacity; 3. hospital admission for more than 48 hours, due to: a.transfer from another hospital to the UMCG; b.transfer from another ward (e.g. Intensive Care Unit (ICU), or rehabilitation center) to an internal medicine ward in the UMCG; 4. expected stay in hospital for less than 48 hours or when the patient is expected to die within

Design outcomes

Primary

MeasureTime frame
main study parameters are repeated measurements of mobility (assessed by De Morton Mobility Index), and perceived fatigue (assessed with the Pittsburgh Fatigability Scale).

Secondary

MeasureTime frame
Secondary objectives are the capacity of the physiologic system to enhance homeostasis during illness is reflected by the capacity of different organ systems to restore deviating values back to normal values. Physiologic systems are expressed by cognitive, immunological, endocrine, musculoskeletal, cardiovascular, respiratory, and renal responses. Furthermore, age, sex, educationlevel, depression, comorbidity, medication, pain, in-hospital activity, and the capacity of the physiologic system to enhance homeostasis will be used in the analyses for the first secondary objective. Finally, in the qualitative interview, feasibility of an intervention to prevent hospital associated decline will be investigated. The use of a wearable (Fitbit) in combination with a digital application will be evaluated using two questions addressing user acceptability.

Countries

Netherlands

Outcome results

None listed

Source: NL-OMON (via WHO ICTRP)