TY - JOUR
T1 - Participant recruitment and attrition in surgical randomised trials with placebo controls versus non-operative controls
T2 - a meta-epidemiological study and meta-analysis
AU - Natarajan, Pragadesh
AU - Menounos, Spiro
AU - Harris, Laura
AU - Monuja, Masiath
AU - Gorelik, Alexandra
AU - Karjalainen, Teemu
AU - Buchbinder, Rachelle
AU - Harris, Ian A.
AU - Naylor, Justine M.
AU - Adie, Sam
N1 - Publisher Copyright:
© Author(s) (or their employer(s)) 2024.
PY - 2024/4
Y1 - 2024/4
N2 - Objective To compare differences in recruitment and attrition between placebo control randomised trials of surgery, and trials of the same surgical interventions and conditions that used non-operative (non-placebo) controls. Design Meta-epidemiological study. Data sources Randomised controlled trials were identified from an electronic search of MEDLINE, EMBASE and Cochrane Central Register of Controlled Trials from their inception date to 21 November 2018. Study selection Placebo control trials evaluating efficacy of any surgical intervention and non-operative control trials of the same surgical intervention were included in this study. 25 730 records were retrieved from our systemic search, identifying 61 placebo control and 38 nonoperative control trials for inclusion in analysis. Outcome measures Primary outcome measures were recruitment and attrition. These were assessed in terms of recruitment rate (number of participants enrolled, as a proportion of those eligible) and overall attrition rate (composite of dropout, loss to follow-up and cross-overs, expressed as proportion of total sample size). Secondary outcome measures included participant cross-over rate, dropout and loss to follow-up. Results Unadjusted pooled recruitment and attrition rates were similar between placebo and non-operative control trials. Study characteristics were not significantly different apart from time to primary timepoint which was shorter in studies with placebo controls (365 vs 274 days, p=0.006). After adjusting for covariates (follow-up duration and number of timepoints), the attrition rate of placebo control trials was almost twice as high compared with non-operative controlled-trials (incident rate ratio (IRR) (95% CI) 1.8 (1.1 to 3.0), p=0.032). The incorporation of one additional follow-up timepoint (regardless of follow-up duration) was associated with reduced attrition in placebo control surgical trials (IRR (95% CI) 0.64 (0.52 to 0.79), p<0.001). Conclusions Placebo control trials of surgery have similar recruitment issues but higher attrition compared with nonoperative (non-placebo) control trials. Study design should incorporate strategies such as increased timepoints for given follow-up duration to mitigate losses to follow-up and dropout.
AB - Objective To compare differences in recruitment and attrition between placebo control randomised trials of surgery, and trials of the same surgical interventions and conditions that used non-operative (non-placebo) controls. Design Meta-epidemiological study. Data sources Randomised controlled trials were identified from an electronic search of MEDLINE, EMBASE and Cochrane Central Register of Controlled Trials from their inception date to 21 November 2018. Study selection Placebo control trials evaluating efficacy of any surgical intervention and non-operative control trials of the same surgical intervention were included in this study. 25 730 records were retrieved from our systemic search, identifying 61 placebo control and 38 nonoperative control trials for inclusion in analysis. Outcome measures Primary outcome measures were recruitment and attrition. These were assessed in terms of recruitment rate (number of participants enrolled, as a proportion of those eligible) and overall attrition rate (composite of dropout, loss to follow-up and cross-overs, expressed as proportion of total sample size). Secondary outcome measures included participant cross-over rate, dropout and loss to follow-up. Results Unadjusted pooled recruitment and attrition rates were similar between placebo and non-operative control trials. Study characteristics were not significantly different apart from time to primary timepoint which was shorter in studies with placebo controls (365 vs 274 days, p=0.006). After adjusting for covariates (follow-up duration and number of timepoints), the attrition rate of placebo control trials was almost twice as high compared with non-operative controlled-trials (incident rate ratio (IRR) (95% CI) 1.8 (1.1 to 3.0), p=0.032). The incorporation of one additional follow-up timepoint (regardless of follow-up duration) was associated with reduced attrition in placebo control surgical trials (IRR (95% CI) 0.64 (0.52 to 0.79), p<0.001). Conclusions Placebo control trials of surgery have similar recruitment issues but higher attrition compared with nonoperative (non-placebo) control trials. Study design should incorporate strategies such as increased timepoints for given follow-up duration to mitigate losses to follow-up and dropout.
UR - http://www.scopus.com/inward/record.url?scp=85191103521&partnerID=8YFLogxK
U2 - 10.1136/bmjopen-2023-080258
DO - 10.1136/bmjopen-2023-080258
M3 - Article
C2 - 38637129
AN - SCOPUS:85191103521
SN - 2044-6055
VL - 14
JO - BMJ Open
JF - BMJ Open
IS - 4
M1 - e080258
ER -