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RAW Study Version 3.4

NCT00280722 · Status: WITHDRAWN · Phase: NA · Type: INTERVENTIONAL

Last updated 2017-11-06

No results posted yet for this study

Summary

The purpose of this study is to investigate the feasibility of carrying out a full scale randomised controlled trial to compare the effects of giving additional information versus no additional information to patients prior to their first oncology appointment.

Hypothesis: Patients with some awareness of research provided prior to clinic appointment in oncology and aware of the possibility of being invited to take part in a clinical trial are more likely to agree to participate.

Conditions

Interventions

BEHAVIORAL

patient information leaflet

Sponsors & Collaborators

  • Liverpool John Moores University

    collaborator OTHER

  • National Cancer Research Network

    collaborator NETWORK

  • Oxford University Hospitals NHS Trust

    lead OTHER

Principal Investigators

  • Susan J Palmer · Thames Valley Cancer Research Network

Study Design

Allocation
RANDOMIZED
Purpose
OTHER

Eligibility

Min Age
18 Years
Sex
ALL
Healthy Volunteers
No

Timeline & Regulatory

Start
2006-01-31
Completion
2006-11-30

Countries

  • United Kingdom

Study Locations

More Related Trials

Entities

Diseases

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 NCT00280722 on ClinicalTrials.gov