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Physiotherapy Led Community Intervention for Older Adults Discharged From the Emergency Department

The Effectiveness of a Physiotherapy Led Community Based Intervention at Reducing Adverse Outcomes in Older Adults Discharged From the Emergency Department: A Pilot Feasibility Randomized Controlled Trial

Status
Completed
Phases
NA
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT04983602
Acronym
EDPLUS
Enrollment
29
Registered
2021-07-30
Start date
2021-09-13
Completion date
2022-06-13
Last updated
2022-07-27

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

Conditions

Health Services for the Aged, Old Age; Debility

Keywords

older adults, geriatric medicine, integrated care, emergency department, feasibility

Brief summary

ED PLUS Emergency Department Discharge Physiotherapy Led Community Service is a pilot feasibility randomized controlled trial investigating the role of an integrated care intervention consisting of comprehensive geriatrics assessment in older adults in the emergency department and a physiotherapy-led community based intervention.

Detailed description

All patients who are aged 65 years and over will be screened using the Identification of Seniors at Risk (ISAR) Tool in the emergency department of a University Teaching Hospital. Those with a score of 2 or above in the ISAR and suitable for discharge home will be randomised. The first treatment arm will undergo geriatric medicine item directed Comprehensive Geriatric Assessment (CGA) from admission to emergency department (ED). The non-treatment arm will under usual patient care. The second treatment arm will undergo geriatric medicine team directed CGA from admission to ED and a physiotherapy led community based 6 week intervention in the patient's home. A dedicated multidisciplinary team of geriatric medicine trainee, occupational therapist, physiotherapist and medical social worker will carry out the assessment. For those randomised to the second treatment arm, a physiotherapist will assess and carry out a 6 week interventions that arise from that assessment and liaise with the patients General Practitioner (GP), medical social worker and other health care professionals. The overall aims of ED PLUS are assess the feasibility of the 6 week physiotherapy led intervention. Feasibility will be determined by the following outcomes: i) Recruitment rate ii) Adherence rate iii) Acceptability of the programme iv) Retention v) Incidents The secondary aims are to improve function, reduce anxiety and depression, improve quality of life and prevent unnecessary ED admission.

Interventions

OTHERComprehensive Geriatric Assessment arm

The intervention will involve a comprehensive geriatric assessment which will be provided by a geriatric doctor, physiotherapist, occupational therapist, social worker, pharmacist and specialist nurse.,

OTHEREDPLUS

EDPLUS involves a 6 week physiotherapy led community based intervention involving 3 home visits and weekly telephone support.

Sponsors

University Hospital of Limerick
CollaboratorOTHER
University of Limerick
Lead SponsorOTHER

Study design

Allocation
RANDOMIZED
Intervention model
PARALLEL
Primary purpose
TREATMENT
Masking
SINGLE (Outcomes Assessor)

Masking description

The outcomes assessor will be unaware if the participant was in usual care, comprehensive geriatric assessment arm or the ED PLUS arm

Eligibility

Sex/Gender
ALL
Age
65 Years to No maximum
Healthy volunteers
No

Inclusion criteria

The inclusion criteria for participants include: * Adults aged ≥65 years with undifferentiated medical complaints presenting to an ED. * Medically stable as deemed by the treating physician * Display a score of ≥2 on the Identification of Seniors at Risk (ISAR) screening tool. * Be community dwelling * Be discharged from the ED within 72 hours of index visit.

Exclusion criteria

include: * Individuals under the age of 65 years. * Have a score of less than 2 on the ISAR. * Older adults who present with acute myocardial infarction, stroke or non-medical problems e.g. surgical or psychiatric issues. * Older adults who are medically unstable will be excluded. * If neither the patient nor carer can communicate in English sufficiently to complete consent or baseline assessment, they will be excluded. * Older adults who are admitted to hospital from the ED will be excluded. * Older adults who have a confirmed COVID 19 diagnosis or those with symptoms highly suggestive of COVID 19 will be excluded.

Design outcomes

Primary

MeasureTime frameDescription
Functional Decline6 weeks post ED visitBarthel Index is global measure of functional status with a score from 0-20. A score of 0 is completely dependent, 20 is fully independent.

Secondary

MeasureTime frameDescription
Patient satisfactionBaseline, 6 weeks post ED visit and 6 months post ED visitPatient satisfaction is determined by the Patient Satisfaction Survey III Short Form (PSQ18). This is scored from 18 to 90, with 18 being the lowest level of satisfaction to 90 being the best score
Rate of ED representationBaseline, 6 weeks post ED visit and 6 months post ED visitA record of the patient coming back to the ED within 6 weeks and/or 6 months post ED index visit
Rate of Hospital readmissionBaseline,6 weeks post ED visit and 6 months post ED visitA record of the patient requiring admission to the hospital within 6 weeks and/or 6 months
Patient Quality of LifeBaseline, 6 weeks post ED visit and 6 months post ED visitPatient rated quality of life is determined by the Euro Quality of Life EQ5D. This scale is scored from 0 to 100 where 0 is the worst imaginable health state with 100 being the best imaginable.
Patient Experience Times6 weeksExact time of admission or discharge form the ED will be collected at 6 weeks post ED index visit
Number of visits to the family doctor or public health nurse6 weeks and 6 months post index ED visitDetermined by self reported visits to family doctor or public health nurse. This will be a telephone consultation at 6 week and 6 months post ED index visit where patients will be asked if they have visited a family doctor or public health nurse in the previous 6 weeks at the 6 week telephone call, or 6 months at the 6 month telephone call
Mortality6 weeks post ED index visit or 6 months post ED index visitA record of the patient having died within 6 weeks or 6 months

Countries

Ireland

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 13, 2026