Adapting the James Lind Alliance priority setting process to better support patient participation: an example from cystic fibrosis.
N J RowbothamS J SmithZ C ElliottP A LeightonO C RaynerR MorleyAlan Robert SmythPublished in: Research involvement and engagement (2019)
Background The James Lind Alliance (JLA) method is well recognised for setting research priorities. The JLA approach involves a combination of surveys and workshop interactions between patients, carers and health care professionals to identify and agree on a "top ten" list of research questions. Respiratory infection is one of the hallmarks of cystic fibrosis (CF). To avoid cross infection, patients are advised not to meet face to face, preventing us following standard JLA methodology. Here we describe adaptations made during our recent JLA Priority Setting Partnership (PSP) in CF. Methods We elicited and prioritised research questions, using sequential online surveys, promoted through social media. People with CF participated in steering committee meetings and the final workshop, using videoconferencing. Alterations to workshop methodology enabled participants attending in person and those joining remotely, to contribute equally. We also altered the JLA methodology to include "lone" questions, asked by only one survey respondent. We are now working with the CF community to co-produce research projects that answer these top ten. Results There were 482 respondents, from 23 countries, who submitted 1080 questions. Increases in the number of responses occurred just after promotion on social media. Use of videoconferencing enabled participation of multiple people with CF and ensured participation from anywhere in the world, including hospital inpatients. Inclusion of lone questions resulted in one being included in our top ten. Conclusions There is no "one-size-fits-all" for patient involvement methodologies. Through altering the JLA methods to fit our patient group we achieved wide participation. We believe that methods used in our project may also be applied to future partnerships to increase participation, especially where people may be hospitalised or be unable to travel. The methodology we are developing through the JLA PSP CF2 project may be useful for other PSPs to follow.
Keyphrases
- cystic fibrosis
- social media
- pseudomonas aeruginosa
- healthcare
- health information
- end stage renal disease
- physical activity
- lung function
- ejection fraction
- newly diagnosed
- chronic kidney disease
- cross sectional
- case report
- quality improvement
- peritoneal dialysis
- patient reported outcomes
- air pollution
- tertiary care
- dna repair
- oxidative stress
- current status
- dna damage
- electronic health record