Skip to main content
editorial
. 2021 Aug 13;37(Suppl 1):113–117. doi: 10.1007/s11606-021-07085-w

Table 1.

Patient Inclusion in the Design of the Study

Patient engagement Goal Outcome
Internet survey of patients’ tapering perceptions (N=250) Identify patient needs and preferences; tailor methods accordingly

- Participation in tapering is voluntary

- Participants randomized to behavioral treatment

- Co-primary outcome (pain intensity, opioid dose)

National patient advisory panel (N=100) Ensure patient-facing study materials are acceptable and pleasing to patients

- Study logo selected by patients

- EMPOWER acronym created by a patient

- Surveys vetted by patients

- Website and brochure vetted by patients

- Peer-to-peer video vignettes offered on website