Informed consent processes Not Applicable Service delivery
Conditions
Interventions
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 inf
Sponsors
Record Provided by the NHSTCT Register - 2004 Update - Department of Health (UK)
Eligibility
Sex/Gender
Female
Inclusion criteria
Inclusion criteria: 1. Age range of subjects 18 - 40 years 2. Female
Exclusion criteria
Exclusion criteria: Not provided at time of registration
Design outcomes
Primary
| Measure | Time frame |
|---|---|
| 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
| Measure | Time frame |
|---|---|
| Not provided at time of registration | — |
Countries
United Kingdom
Outcome results
None listed