Study to measure the impact of a speaking book on patient Understanding of clinical research knowledge.
Not Applicable
- Conditions
- Health Condition 1: Z768- Persons encountering health services in other specified circumstances
- Registration Number
- CTRI/2024/06/068453
- Lead Sponsor
- ovartis Healthcare Pvt Ltd.
- Brief Summary
Not available
- Detailed Description
Not available
Recruitment & Eligibility
- Status
- ot Yet Recruiting
- Sex
- Not specified
- Target Recruitment
- 0
Inclusion Criteria
1. Informed consent
2. Male and females
3. Minimum age 18 years
4. Minimal literacy levels as verified by Principle Investigator/Study Team
5. Disease of benign haemoglobinopathies
6. Patients who have never participated in a clinical trial previously.
Exclusion Criteria
1. Patients who are unable to comprehend or are unwilling to sign an informed consent form (ICF)
2. Any medical condition that, in the opinion of the Investigator, would interfere with completion of the study such as psychiatric.
Study & Design
- Study Type
- Interventional
- Study Design
- Not specified
- Primary Outcome Measures
Name Time Method To evaluate the Improvement in clinical trial knowledge with the Speaking Book. At least a 25 percent improvement in willingnessTimepoint: Visit 1: Baseline and Visit 2: Approx 4 wks (+/-) 2 wks
- Secondary Outcome Measures
Name Time Method To assess the willingness to participate in a clinical trial after reviewing the Speaking Book. At least a 25 percent improvement in willingness to participate in a clinical trialTimepoint: Visit 1 Baseline <br/ ><br>Visit 2 Approx 4 wks plus or minus 2 wks