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Clinical Trial Details — Status: Completed

Administrative data

NCT number NCT01414543
Other study ID # UEL1
Secondary ID
Status Completed
Phase N/A
First received August 10, 2011
Last updated May 10, 2016
Start date October 2009
Est. completion date October 2012

Study information

Verified date August 2009
Source University of East London
Contact n/a
Is FDA regulated No
Health authority United Kingdom: National Health Service
Study type Interventional

Clinical Trial Summary

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.


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.


Recruitment information / eligibility

Status Completed
Enrollment 10
Est. completion date October 2012
Est. primary completion date October 2012
Accepts healthy volunteers Accepts Healthy Volunteers
Gender Both
Age group 24 Years to 65 Years
Eligibility Inclusion Criteria:

- Psychologist's who have experienced client violence

Exclusion Criteria:

Study Design

Allocation: Non-Randomized, Intervention Model: Single Group Assignment, Masking: Open Label, Primary Purpose: Health Services Research


Related Conditions & MeSH terms


Intervention

Other:
Information Sheet
Providing the Participant with information regarding the aim of the experiment
Consent
Providing a consent form for participants. The participant is aware of his or her rights
interview
participants will interviewed by fardin jussab for approximately one hour regarding their experience of client violence
Debrief
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.

Locations

Country Name City State
United Kingdom National Health Service London

Sponsors (1)

Lead Sponsor Collaborator
University of East London

Country where clinical trial is conducted

United Kingdom, 

Outcome

Type Measure Description Time frame Safety issue
Primary experience of violence participant's discuss their experince of client violence in the work place one hour Yes
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