1. Referral to study team by health authorities |
– Collaborate with referral partners to obtain participant contact information, preferred modes and times of contact, consent for initial contact |
– Assign each participant to one field interviewer throughout the study, where possible |
2. Initial contact (telephone) |
– Contact participant using study cell phone with text and email functions |
– Use different modes and times of contact and obtain three alternative contacts |
– Answer questions and offer flexibility in timing and location of interview |
– Provide 24-h reminders using preferred communication mode (e.g., text messages) |
– Enquire at each encounter if there is a change in contact information |
– Accommodate interview rescheduling |
3. Baseline interview (in-person) |
– Establish rapport using effective communication techniques |
– Adopt a professional (neutral, non-judgmental) manner |
– Apply risk-mitigation training (interviewer safety) |
– Provide essential study materials outlining the research process and interview dates |
– Explain study purpose and confidentiality, answering questions and providing time to consider |
– Use visual aids to convey the type, length and timing of research interviews |
– Verify eligibility and obtain written informed consent |
– Verify contact information and alternative contacts |
– Use audio aids for survey items sensitive to reporting bias |
– Provide meaningful honoraria such as gift cards for local department stores |
– Collect information to facilitate rapport at follow-up interviews, such as preferred name |