MedPath

A randomised phase III trial evaluating the efficacy of more intensive written information in patients having radical radiation therapy.

Phase 3
Recruiting
Conditions
Anxiety levels
Patient satisfaction.
Mental Health - Anxiety
Registration Number
ACTRN12605000705684
Lead Sponsor
Perth Radiation Oncology Centre
Brief Summary

Not available

Detailed Description

Not available

Recruitment & Eligibility

Status
Recruiting
Sex
All
Target Recruitment
212
Inclusion Criteria

The patient must be having radical radiotherapy.The patient must have a good understanding of english.The patient must be able to complete questionnaire unaided.Used only for patients diagnosed with Breast,Lung,Prostate,Rectal and Gynaecological cancer.

Exclusion Criteria

A poor understanding of written english.Significant visual impairment and previous radiation therapy.

Study & Design

Study Type
Interventional
Study Design
Not specified
Primary Outcome Measures
NameTimeMethod
The primary outcome is anxiety scores[Measured initially (prior to intervention) and following the intervention at 2 intervals (pre and post radiotherapy).]
Secondary Outcome Measures
NameTimeMethod
The secondary outcome is patient satisfaction.[This is measured following the intervention and prior to commencing radiotherapy.]
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