Skip to main content
OpenTrials
Completed

NCT Number: NCT04983602

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

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.

Completed

Looking for future studies?

Notify Me

Key information

Age range

65 year and older

Sex eligibility

All sexes

Study type

Interventional

Phase

Not applicable

Primary location

University Hospital Limerick

Limerick, Ireland

About this study

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.

Who can participate

Healthy volunteers accepted: No

Only the study team can determine whether someone qualifies for participation.

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.

Treatment and study plan

Comprehensive Geriatric Assessment arm

Other

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.,

EDPLUS

Other

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

Primary outcomes

  1. Functional Decline

    Time frame: 6 weeks post ED visit

    Barthel Index is global measure of functional status with a score from 0-20. A score of 0 is completely dependent, 20 is fully independent.

  2. Functional Decline

    Time frame: 6 months post ED visit

    Barthel 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 outcomes

  1. Patient Quality of Life

    Time frame: Baseline, 6 weeks post ED visit and 6 months post ED visit

    Patient 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.

  2. Patient satisfaction

    Time frame: Baseline, 6 weeks post ED visit and 6 months post ED visit

    Patient 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

  3. Rate of ED representation

    Time frame: Baseline, 6 weeks post ED visit and 6 months post ED visit

    A record of the patient coming back to the ED within 6 weeks and/or 6 months post ED index visit

  4. Rate of Hospital readmission

    Time frame: Baseline,6 weeks post ED visit and 6 months post ED visit

    A record of the patient requiring admission to the hospital within 6 weeks and/or 6 months

  5. Mortality

    Time frame: 6 weeks post ED index visit or 6 months post ED index visit

    A record of the patient having died within 6 weeks or 6 months

  6. Patient Experience Times

    Time frame: 6 weeks

    Exact time of admission or discharge form the ED will be collected at 6 weeks post ED index visit

  7. Number of visits to the family doctor or public health nurse

    Time frame: 6 weeks and 6 months post index ED visit

    Determined 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

Sponsors and collaborators

Lead sponsor

University of Limerick

Other

Collaborators

  • University Hospital of Limerick

Registry information

Official study title

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

Acronym: EDPLUS

Important dates

Study start
2021
Primary completion
2022
Study completion
2022
First posted
Jul 30, 2021
Registry last updated
Jul 27, 2022

OpenTrials presents study information sourced from ClinicalTrials.gov. The official registry record should be consulted for the latest information.

View the official ClinicalTrials.gov record (opens in a new tab)

This listing is for discovery and informational purposes only. It is not medical advice, does not guarantee that a study is recruiting, and does not determine eligibility. Contact the study team and a qualified healthcare professional when considering participation.

Published trials that share one or more normalized conditions with this study.