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Search / Trial NCT04866511

Video NET With CYP Who Witnessed Domestic Violence

Launched by UNIVERSITY OF NOTTINGHAM · Apr 28, 2021

Trial Information

Current as of July 21, 2025

Completed

Keywords

Post Traumatic Stress Narrative Exposure Therapy Children And Young People Domestic Violence Case Study Series

ClinConnect Summary

The purpose of the study is to investigate the potential effectiveness, feasibility, acceptability and putative mechanisms of change of video NET with children and young people who witnessed domestic violence.

The primary objective of the study is to evaluate whether video NET can reduce PTS in this group.

The secondary objectives of the study are:

* To determine whether video NET can also impact on general psychological distress and functioning;
* To examine the putative mechanisms of change within NET, i.e. habituation and integration of trauma memories;
* To explore the feasibility an...

Gender

ALL

Eligibility criteria

  • Inclusion Criteria - Participants must:
  • Be aged 12- 17;
  • Have witnessed domestic violence in the past;
  • Be experiencing clinical levels of post-traumatic stress, as assessed by a member of the CAMHS team;
  • Be on the waiting list to receive trauma-focused treatment;
  • If 16 or over, be able to consent to take part, as assessed by a member of the CAMHS team;
  • If under 16, have at least one person with parental authority who can consent for them. These young people will also be asked to provide their assent;
  • Be able to communicate verbally and speak English;
  • Have access to a device with a webcam and Internet broadband to enable participation in video sessions;
  • Have access to a mobile device, e.g. a smartphone or a tablet. Can be the same as the device above.
  • Exclusion Criteria - Participants will be excluded from the study if:
  • They have a known diagnosis of Intellectual Disability;
  • They have a current high level of risk including of self-harm, suicide or current exposure to domestic violence, as assessed by a member of the CAMHS team;
  • They are substance dependent.

About University Of Nottingham

The University of Nottingham is a leading research institution renowned for its commitment to advancing healthcare through innovative clinical trials. With a strong emphasis on interdisciplinary collaboration, the university harnesses cutting-edge research and expert faculty to address pressing medical challenges. Through its dedicated clinical trials unit, the University of Nottingham conducts rigorous studies aimed at improving patient outcomes and contributing to the global body of medical knowledge. The institution prioritizes ethical practices and participant safety, ensuring that all trials are designed to uphold the highest standards of scientific integrity and regulatory compliance.

Locations

Lincoln, , United Kingdom

Nottingham, Nottinghamshire, United Kingdom

Lincoln, Lincolnshire, United Kingdom

Patients applied

0 patients applied

Trial Officials

Thomas Schröder, PhD

Study Director

University of Nottingham

Sarah Wilde, DClinPsy

Study Director

University of Lincoln

Fiammetta Rocca, Trainee Clinical Psychologist, MSc

Principal Investigator

University of Nottingham

Nima Moghaddam, PhD, DClinPsy

Study Director

University of Lincoln

Timeline

First submit

Trial launched

Trial updated

Estimated completion

Not reported

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