Psychologists' Lived Experience of Client Violence

NCT ID: NCT01414543

Last Updated: 2016-05-11

Study Results

Results pending

The study team has not published outcome measurements, participant flow, or safety data for this trial yet. Check back later for updates.

Basic Information

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Recruitment Status

COMPLETED

Clinical Phase

NA

Total Enrollment

10 participants

Study Classification

INTERVENTIONAL

Study Start Date

2009-10-31

Study Completion Date

2012-10-31

Brief Summary

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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.

Detailed Description

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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.

Conditions

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Life Experiences

Study Design

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Allocation Method

NON_RANDOMIZED

Intervention Model

SINGLE_GROUP

Primary Study Purpose

HEALTH_SERVICES_RESEARCH

Blinding Strategy

NONE

Study Groups

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providing information sheet

providing participants with information regarding the purpose of the research

Group Type OTHER

Information Sheet

Intervention Type OTHER

Providing the Participant with information regarding the aim of the experiment

Seeking consent

Group Type OTHER

Consent

Intervention Type OTHER

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

Interview Participant

Group Type OTHER

interview

Intervention Type OTHER

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

Debrief

The Participants will be debriefed after the interview.

Group Type OTHER

Debrief

Intervention Type OTHER

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.

Interventions

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Information Sheet

Providing the Participant with information regarding the aim of the experiment

Intervention Type OTHER

Consent

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

Intervention Type OTHER

interview

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

Intervention Type 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.

Intervention Type OTHER

Eligibility Criteria

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Inclusion Criteria

* Psychologist's who have experienced client violence

Exclusion Criteria

\-
Minimum Eligible Age

24 Years

Maximum Eligible Age

65 Years

Eligible Sex

ALL

Accepts Healthy Volunteers

Yes

Sponsors

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University of East London

OTHER

Sponsor Role lead

Responsible Party

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Fardin Jussab

Dr

Responsibility Role PRINCIPAL_INVESTIGATOR

Principal Investigators

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Helen Murphy, BA, MSc, DPhil

Role: STUDY_CHAIR

University of East London

Locations

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National Health Service

London, , United Kingdom

Site Status

Countries

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United Kingdom

Other Identifiers

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UEL1

Identifier Type: -

Identifier Source: org_study_id

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