World Health Organization site
Skip Navigation Links

Main
Note: This record shows only 22 elements of the WHO Trial Registration Data Set. To view changes that have been made to the source record, or for additional information about this trial, click on the URL below to go to the source record in the primary register.
Register: ISRCTN
Last refreshed on: 13 January 2015
Main ID:  ISRCTN24829815
Date of registration: 30/09/2004
Prospective Registration: No
Primary sponsor: Record Provided by the NHSTCT Register - 2004 Update - Department of Health (UK)
Public title: Video information to support the process of obtaining informed consent: using foetal tissue for brain tumour research
Scientific title: A randomised controlled trial of the use of video information to support the process of obtaining informed consent: to use foetal tissue for brain tumour research
Date of first enrolment: 30/01/2002
Target sample size: 20
Recruitment status: Completed
URL:  http://isrctn.com/ISRCTN24829815
Study type:  Interventional
Study design:  Randomised controlled trial (Screening)  
Phase: 
Countries of recruitment
United Kingdom
Contacts
Name: DA    Walker
Address:  Academic Division of Child Health School of Human Development E Floor East Block University Hospital NG7 2UH Nottingham United Kingdom
Telephone: +44 (0)115 924 9924 ext 43324/41727
Email: david.walker@nottingham.ac.uk
Affiliation: 
Name:    
Address: 
Telephone:
Email:
Affiliation: 
Key inclusion & exclusion criteria
Inclusion criteria: 1. Age range of subjects 18 - 40 years
2. Female

Exclusion criteria: Not provided at time of registration

Age minimum:
Age maximum:
Gender: Female
Health Condition(s) or Problem(s) studied
Informed consent processes
Not Applicable
Service delivery
Intervention(s)
Randomised controlled trial to assess whether the use of recorded media (video tape) within the informed consent process is as acceptable, feasible and informative as the conventional face-to-face informed consent processes used in current clinical practice.
Primary Outcome(s)
1. Patient assessment of acceptability
2. Patient anxiety levels
3. Patient level of relevant knowledge
4. Patient degree of satisfaction
5. Clinical feasibility and acceptability of the different methods of obtaining informed consent
Secondary Outcome(s)
Not provided at time of registration
Secondary ID(s)
N0192107555
Source(s) of Monetary Support
Queen's Medical Centre University Hospital NHS Trust (UK)
Secondary Sponsor(s)
Ethics review
Results
Results available:
Date Posted:
Date Completed:
URL:
Disclaimer: Trials posted on this search portal are not endorsed by WHO, but are provided as a service to our users. In no event shall the World Health Organization be liable for any damages arising from the use of the information linked to in this section. None of the information obtained through use of the search portal should in any way be used in clinical care without consulting a physician or licensed health professional. WHO is not responsible for the accuracy, completeness and/or use made of the content displayed for any trial record.
Copyright - World Health Organization - Version 3.6 - Version history