- ICH GCP
- US Clinical Trials Registry
- Clinical Trial NCT01414543
Psychologists' Lived Experience of Client Violence
May 10, 2016 updated by: Fardin Jussab, University of East London
Counselling and Clinical Psychologists Lived Experience of Client Violence
The objective of the proposed research is to gain a detailed understanding and account of psychologists' experience of client violence in clinical practice.
The emphasis is upon a detailed understanding of how psychologists perceive and understand their experience of client violence and its impact upon their identity as clinicians and as individuals.
Study Overview
Status
Completed
Conditions
Intervention / Treatment
Detailed Description
This research is interested in Counselling and Clinical Psychologists who have experienced client violence at their work place.
The main research question being asked is how do psychologists' understand their personal experiences of client violence.
This is an important and interesting subject for Counselling and Clinical Psychologists as it provides a detailed personal account of the implications of violence upon their personal and professional identity, psychological well being and how they define violence.
Furthermore, this research may help facilitate in designing a specific policy and help future research to issue guidelines for counselling and clinical psychologists in order to keep themselves safe within their professional practice.
Psychologists working for the National Health Service will be recruited and provided with information regarding the research aims and objectives.
There will be interviews held at their place of work for approximately one hour.
Study Type
Interventional
Enrollment (Anticipated)
10
Phase
- Not Applicable
Contacts and Locations
This section provides the contact details for those conducting the study, and information on where this study is being conducted.
Study Locations
-
-
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London, United Kingdom
- National Health Service
-
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Participation Criteria
Researchers look for people who fit a certain description, called eligibility criteria. Some examples of these criteria are a person's general health condition or prior treatments.
Eligibility Criteria
Ages Eligible for Study
24 years to 65 years (Adult, Older Adult)
Accepts Healthy Volunteers
Yes
Genders Eligible for Study
All
Description
Inclusion Criteria:
- Psychologist's who have experienced client violence
Exclusion Criteria:
-
Study Plan
This section provides details of the study plan, including how the study is designed and what the study is measuring.
How is the study designed?
Design Details
- Primary Purpose: Health Services Research
- Allocation: Non-Randomized
- Interventional Model: Single Group Assignment
- Masking: None (Open Label)
Arms and Interventions
Participant Group / Arm |
Intervention / Treatment |
---|---|
Other: providing information sheet
providing participants with information regarding the purpose of the research
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Providing the Participant with information regarding the aim of the experiment
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Other: Seeking consent
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Providing a consent form for participants.
The participant is aware of his or her rights
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Other: Interview Participant
|
participants will interviewed by fardin jussab for approximately one hour regarding their experience of client violence
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Other: Debrief
The Participants will be debriefed after the interview.
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at the end of each interview the researcher will ask participants whether the emotions aroused in the interview require further discussions.
Interviewees will be also advised that should they wish to talk further about any topics covered the in the interview, they could telephone the researcher at a later time.
There will also be leaflets of supporting agencies.
|
What is the study measuring?
Primary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
---|---|---|
experience of violence
Time Frame: one hour
|
participant's discuss their experince of client violence in the work place
|
one hour
|
Collaborators and Investigators
This is where you will find people and organizations involved with this study.
Sponsor
Investigators
- Study Chair: Helen Murphy, BA, MSc, DPhil, University of East London
Study record dates
These dates track the progress of study record and summary results submissions to ClinicalTrials.gov. Study records and reported results are reviewed by the National Library of Medicine (NLM) to make sure they meet specific quality control standards before being posted on the public website.
Study Major Dates
Study Start
October 1, 2009
Primary Completion (Actual)
October 1, 2012
Study Completion (Actual)
October 1, 2012
Study Registration Dates
First Submitted
August 10, 2011
First Submitted That Met QC Criteria
August 10, 2011
First Posted (Estimate)
August 11, 2011
Study Record Updates
Last Update Posted (Estimate)
May 11, 2016
Last Update Submitted That Met QC Criteria
May 10, 2016
Last Verified
August 1, 2009
More Information
Terms related to this study
Keywords
Other Study ID Numbers
- UEL1
This information was retrieved directly from the website clinicaltrials.gov without any changes. If you have any requests to change, remove or update your study details, please contact register@clinicaltrials.gov. As soon as a change is implemented on clinicaltrials.gov, this will be updated automatically on our website as well.
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