Table 1 Interview guide
Health belief model construct/mediating factors | Question(s) |
|---|---|
Perceived Susceptibility | How would you describe your health prior to CLD? |
Is there anything that you could have done differently to avoid getting CLD? | |
Is there anything that people can do to avoid getting CLD? | |
Perceived Severity | How did you feel when you were diagnosed with (or discovered that you had) CLD? |
How has CLD affected your life? | |
What does having CLD mean to you? | |
Perceived Benefits | What treatments have you had for CLD? |
How have these treatments affected you? | |
Perceived Barriers | Have there been any obstacles that you have encountered in getting treatment for CLD? |
What needs to be done to restore you to optimum health? | |
Do you anticipate that you’ll fully recover from CLD? | |
What have the doctors that have least helped your CLD not done for you? | |
Cues to Action | What kinds of support (community, family, friends, health care providers, CLD support groups, internet newsgroups, CLD activism groups, etc.) have you had during your CLD? |
How have these support systems affected your CLD? | |
What motivates you in your struggle with CLD? | |
Self Efficacy | What can doctors do to more effectively care for patients with CLD? |
What can the community do to best support people with CLD? | |
CLD Diagnosis and Healthcare System | Why does CLD best fit your symptoms? |
Have you ever doubted that you have CLD? | |
How do you think conventional health care providers view CLD patients? | |
How do you think LLMDs view CLD patients? | |
What have the doctors that have helped your CLD the most done for you? |