World Health Organization site
Skip Navigation Links

Main
Note: This record shows only 22 elements of the WHO Trial Registration Data Set. To view changes that have been made to the source record, or for additional information about this trial, click on the URL below to go to the source record in the primary register.
Register: ANZCTR
Last refreshed on: 10 December 2019
Main ID:  ACTRN12617000729325
Date of registration: 19/05/2017
Prospective Registration: Yes
Primary sponsor: Kathy Stiller
Public title: Levels of distress and anxiety in patients after trauma and their next-of-kin while in hospital
Scientific title: Levels of distress and anxiety in acute trauma patients and their next-of-kin throughout the period of hospitalisation
Date of first enrolment: 01/10/2017
Target sample size: 50
Recruitment status: Withdrawn
URL:  https://anzctr.org.au/ACTRN12617000729325.aspx
Study type:  Observational
Study design:  Purpose: Natural history;Duration: Longitudinal;Selection: Convenience sample;Timing: Prospective;  
Phase:  Not Applicable
Countries of recruitment
Australia
Contacts
Name: Dr Kathy Stiller   
Address:  L4 Allied Health Building Royal Adelaide Hospital North Terrace Adelaide South Australia 5000 Australia
Telephone: +61 8 82225334
Email: Kathy.Stiller@sa.gov.au
Affiliation: 
Name: Dr Kathy Stiller   
Address:  L4 Allied Health Building Royal Adelaide Hospital North Terrace Adelaide South Australia 5000 Australia
Telephone: +61 8 82225334
Email: Kathy.Stiller@sa.gov.au
Affiliation: 
Key inclusion & exclusion criteria
Inclusion criteria: All patients admitted to the Intensive Care Unit of the Royal Adelaide Hospital following trauma under the auspices of the Acute Surgical Unit or Neurosurgery Department who are referred for social work assessment and intervention, and their next-of-kin who is visiting the patient (i.e. not involved in the traumatic injury).
Exclusion criteria: Patients or next-of-kin who refuse consent or are unable to communicate effectively and easily in English (e.g. insufficient understanding of English, cognitive impairment, psychiatric condition). In the clinical scenario where the patient is unable to communicate as a result of their traumatic injury, or the treatment thereof, the patient’s next-of-kin will be invited to participate in the study and the patient only approached regarding participation once they are able to communicate effectively in English.

Age minimum: 18 Years
Age maximum: No limit
Gender: Both males and females
Health Condition(s) or Problem(s) studied
Injuries and Accidents - Other injuries and accidents
Mental Health - Anxiety
trauma;intensive care;Mental health;
trauma
intensive care
Mental health
Intervention(s)
No aspect of usual care will be changed as a result of the current study. In particular, social work assessment and interventions will be provided as per usual practice. Participation in this study will involve completing two 'questionnaires'. One will take approximately 30 seconds to complete and the other 5 to 10 minutes. The questionnaires will be completed three times: once as soon as possible post-admission to hospital, then on transfer to a general ward and then just prior to hospital discharge. The duration of the observation period will be variable depending on the length of hospital stay.
Primary Outcome(s)
Depression Anxiety and Stress Scale (21 items)[As soon as possible after hospital admission, after transfer to the general ward and a few days prior to hospital discharge.]
Subjective Units of Distress Scale[As soon as possible after hospital admission, after transfer to the general ward and a few days prior to hospital discharge.]
Secondary Outcome(s)
Amount of social work intervention (total number of interventions and total duration of interventions). These data will be retrieved from databases already in use where allied health interventions, including social work, are recorded.[Throughout hospital admission.]
Secondary ID(s)
None
Source(s) of Monetary Support
Secondary Sponsor(s)
Manoj Pereira
Ethics review
Status: Approved
Approval date:
Contact:
Royal Adelaide Hospital Research Ethics Committee
Results
Results available:
Date Posted:
Date Completed:
URL:
Disclaimer: Trials posted on this search portal are not endorsed by WHO, but are provided as a service to our users. In no event shall the World Health Organization be liable for any damages arising from the use of the information linked to in this section. None of the information obtained through use of the search portal should in any way be used in clinical care without consulting a physician or licensed health professional. WHO is not responsible for the accuracy, completeness and/or use made of the content displayed for any trial record.
Copyright - World Health Organization - Version 3.6 - Version history