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Table 3 FGD and KII participant’s perceptions on what their communities would view as facilitators and barriers to HIV research participation, August-October 2006

From: “Research participants want to feel they are better off than they were before research was introduced to them”: engaging cameroonian rural plantation populations in HIV research

 

Facilitators

·

Improves general community welfare

·

Provides comprehensive health services by offering care and treatment for common illnesses

·

Protects personal information

·

Provides incentives

·

Incorporates community input in the planning and implementation phases

·

Avoids or minimizes disruptions to ‘everyday life’

 

Barriers

·

Further fuels fears of HIV test

·

Mistrust of researchers (treated as guinea pigs; fail to keep participant information confidential and private)

·

Requires people to take time away from work or other important activities

·

Access to medical care and treatment difficult or costly, or care and treatment is second-rate

·

Promotes risk-taking behaviours

·

Requires abstaining from alcohol use and sex