Mainstreaming Study

Not Applicable

Registration Number: CTRI/2022/05/042558

Lead Sponsor: Rima Sanjay Pathak

Brief Summary: Not available

Detailed Description: Not available

Recruitment & Eligibility

Status: Open to Recruitment

Sex: Not specified

Target Recruitment: 0

Inclusion Criteria

Inclusion Criteria (Patients/ Caregivers)

1. Patients and or their caregivers from the breast, gynecology, pediatric, central nervous system and colorectal disease management group who are =18 years of age and willing to participate in the study

2. Parents or caregivers of the pediatric patients

3. Can read at least 1 language in which the written informed consent and pamphlets are provided

4. Patients who have a confirmed diagnosis of cancer OR healthy individuals who are suspected or known carriers of a pathogenic variant in a cancer predisposing gene

5. Patients who can understand the language in which the survey is conducted and in which the information is provided in the pamphlets and/ the audio-visual aids

Inclusion criteria (Physicians):

1. All physicians participating in the care of cancer patients and willing to consent for participation in the study and

2. All those that agree to allow access to their background analytics data and

3. Working at the Tata Memorial Centre

Exclusion Criteria

Exclusion Criteria (Patient/ Caregivers):

1. Those who have a life expectancy of =3 months

2. Pediatric patients younger than 18 years of age

3. Those who cannot understand written or spoken language in which the survey is served and the information is provided.

4. Those who cannot read the languages in which the pamphlets are provided.

Exclusion Criteria (Physicians):

1. Those who do not permit access to their background analytics data

Study & Design

Study Type: Interventional

Study Design: Not specified

Primary Outcome Measures

Name	Time	Method
Primary Objective (Patients): <br/ ><br>1. Determine the impact of audio-visual aids and pamphlets on the awareness, attitudes and expectation of the patients <br/ ><br> <br/ ><br>Primary objective (Physicians): <br/ ><br>1. Evaluate the impact of the cancer genetics training module on the referral rates and patterns of referrals to the cancer genetics clinic at the Tata Memorial Centre for 3 months after the planned interventionTimepoint: Baseline will be recorded 3 months prior to the intervention and )providing educational material) and for 3 months after providing the intervention (educational material)

Secondary Outcome Measures