The Impacts of a Visiting Companion Animal Program on the Health and Wellbeing of Patients whilst Residing in an Acute Care Setting

ISRCTN ISRCTN37522543
DOI https://doi.org/10.1186/ISRCTN37522543
Secondary identifying numbers N/A
Submission date
16/11/2005
Registration date
16/03/2006
Last edited
16/03/2006
Recruitment status
No longer recruiting
Overall study status
Completed
Condition category
Mental and Behavioural Disorders
Prospectively registered
Protocol
Statistical analysis plan
Results
Individual participant data
Record updated in last year

Plain English summary of protocol

Not provided at time of registration

Contact information

Ms Lauren Prosser
Scientific

221 Burwood Highway
Burwood
3125
Australia

Phone +61 (0)3 9244 6452
Email lauren.prosser@deakin.edu.au

Study information

Study designThe study is an open randomised controlled trial using an interventional technique. Measurement involves quality of life and wellbeing scales, a pet attitude scale and observation.
Primary study designInterventional
Secondary study designRandomised controlled trial
Study setting(s)Hospital
Study typeQuality of life
Scientific title
Study objectivesThe implementation of a companion animal program has significant potential for enhancing the wellbeing of neurological unit patients within a hospital setting
Ethics approval(s)Approved by the Melbourne Health Ethics Committee, Deakin University (DU-HREC) on 20/09/2004, reference number: 212-2004
Health condition(s) or problem(s) studiedNeurological disorder
InterventionExperimental group receive visitations from a companion animal program. Control group receive visitations without a companion animal program.
Intervention typeOther
Primary outcome measure1. Assessment of wellbeing due to interventions
2. Assessment of quality of life due to interventions
Secondary outcome measuresAssessing the influence of the interventions on patients within the neurological ward
Overall study start date14/02/2004
Completion date14/02/2007

Eligibility

Participant type(s)Patient
Age groupAdult
SexBoth
Target number of participants80
Key inclusion criteriaParticipants in the study must be a patient on the stroke ward at Western Hospital
Key exclusion criteriaParticipants who are unable to complete the measures for the study
Date of first enrolment14/02/2004
Date of final enrolment14/02/2007

Locations

Countries of recruitment

  • Australia

Study participating centre

221 Burwood Highway
Burwood
3125
Australia

Sponsor information

Deakin University (Australia)
University/education

221 Burwood Highway
Burwood
3125
Australia

Phone +61 (0)3 9244 6452
Email lauren.prosser@deakin.edu.au
Website http://www.deakin.edu.au/hbs/hsd/research/niche
ROR logo "ROR" https://ror.org/02czsnj07

Funders

Funder type

University/education

Deakin University
Government organisation / Universities (academic only)
Alternative name(s)
Deakin, Deakin University in Australia, Gordon Institute of Technology, Geelong State College, Victoria College and antecedent institutions, Gordon Institute of TAFE, Universitas Deakinensis, Deakin University South Asia
Location
Australia

Results and Publications

Intention to publish date
Individual participant data (IPD) Intention to shareNo
IPD sharing plan summaryNot provided at time of registration
Publication and dissemination planNot provided at time of registration
IPD sharing plan