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Frailty Status and Increased Risk for Falls

S

Saglik Bilimleri Universitesi

Status

Enrolling

Conditions

Frailty
Anticholinergic Toxicity
Fall

Treatments

Diagnostic Test: Fall assessment

Study type

Observational

Funder types

Other

Identifiers

NCT04233541
2016/1648-463

Details and patient eligibility

About

We hypothesized that the use of anticholinergic medications may precipitate falls differently by frailty status in older adults. Community-dwelling older subjects admitted to the Geriatrics Outpatient Clinic prospectively enter into the study. Frailty status is defined according to the Physical Frailty Phenotype. The drugs are categorized according to the ACB scale

Full description

Previous studies have found that the use of drugs with anticholinergic properties relate to increased prevalence of falls in older women and men. Frailty is associated with serious health outcomes including falls, hip fractures, and death. Frailty can be a relevant target to investigate its association with the risk of falls among the users of drugs with anticholinergic properties. A recent evidence suggests that the interaction between being frail and adverse outcomes in older adults receiving polypharmacy or centrally acting drugs is complex and not straightforward across all frailty phenotypes.

We classify the participants frail if they met at least three of five criteria, while those having one or two criteria were pre-frail, and others were non-frail. We determine the anticholinergic burden by using the Anticholinergic Cognitive Burden (ACB) Scale developed by Boustani et al.

Enrollment

1,000 estimated patients

Sex

All

Ages

65+ years old

Volunteers

Accepts Healthy Volunteers

Inclusion criteria

  • Community-dwelling older adults

Exclusion criteria

  • a history of dementia,
  • current delirium or psychotic symptoms,
  • taking antipsychotic medications,
  • being functionally dependent to others,
  • difficulty in communicating with the interviewer,
  • terminal illness,
  • being bedridden or wheelchair bound (≥2 weeks),
  • difficulty in standing or walking,
  • incomplete data

Trial design

1,000 participants in 2 patient groups

Fallers
Description:
Participants who reported one or more falls within the 12 months preceding the study consist the group of ''fallers''.
Treatment:
Diagnostic Test: Fall assessment
Non-fallers
Description:
Participants with no fall history consist the group of ''non-fallers''
Treatment:
Diagnostic Test: Fall assessment

Trial contacts and locations

1

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Central trial contact

Mehmet I Naharci, Assoc.Prof.

Data sourced from clinicaltrials.gov

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