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Psychologists' Lived Experience of Client Violence

NCT01414543 · Status: COMPLETED · Phase: NA · Type: INTERVENTIONAL · Enrollment: 10

Last updated 2016-05-11

No results posted yet for this study

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.

Conditions

  • Life Experiences

Interventions

OTHER

Information Sheet

Providing the Participant with information regarding the aim of the experiment

OTHER

Consent

Providing a consent form for participants. The participant is aware of his or her rights

OTHER

interview

participants will interviewed by fardin jussab for approximately one hour regarding their experience of client violence

OTHER

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.

Sponsors & Collaborators

  • University of East London

    lead OTHER

Principal Investigators

  • Helen Murphy, BA, MSc, DPhil · University of East London

Study Design

Allocation
NON_RANDOMIZED
Purpose
HEALTH_SERVICES_RESEARCH
Masking
NONE
Model
SINGLE_GROUP

Eligibility

Min Age
24 Years
Max Age
65 Years
Sex
ALL
Healthy Volunteers
Yes

Timeline & Regulatory

Start
2009-10-31
Primary Completion
2012-10-31
Completion
2012-10-31

Countries

  • United Kingdom

Study Locations

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Read the full study record

This page highlights key information. For complete eligibility criteria, study locations, investigator contacts, and the full protocol, visit the original record on ClinicalTrials.gov.

View NCT01414543 on ClinicalTrials.gov