Improving the depth of data quality or increasing confusion? Reflections on a data analysis involving members of a self‐help group for relatives of people living with dementia

Abstract

Background

Public involvement in research to improve data quality and to empower different stakeholders is good scientific practice, but rarely implemented across all research phases.

Objective

This article reports on an attempt to involve members of a self‐help group for relatives of people living with dementia as co‐researchers in the data analysis in a short‐term format.

Methods

One researcher identified statements about assistive technologies from 17 interviews with people living with dementia and informal caregivers. Two researchers and six co‐researchers independently assigned pre‐defined values to these statements. Subsequently, we compared the values of the researchers and co‐researchers.

Results

The members of the self‐help group identified four original values not considered by the researchers: consent, inclusion, participation and respect.

Discussion

The involvement of co‐researchers led to an improvement in the depth of data quality through the joint identification of values concerning assistive technology. Language barriers between researchers, co‐researchers and interview participants impeded the data analysis.

Conclusion

The challenges and benefits of a participatory data analysis shown here can provide a basis for recommendations for target group‐specific research involvement. Our recommendations relate to the recruitment of co‐researchers, requirements for conducting a participatory data analysis and the participation degree of people involved.

Patient or Public Contribution

The group of co‐researchers participating in the data analysis consisted of relatives of people living with dementia.