Mittal Rajat, Harris Ian A, Adie Sam, Naylor Justine M
Whitlam Orthopaedic Research Centre, Orthopaedic Department, Locked Bag 7103, Liverpool BC, NSW 1871, Australia.
Ingham Institute for Applied Medical Research, Orthopaedic Department, Locked Bag 7103, Liverpool BC, NSW 1871, Australia.
Contemp Clin Trials Commun. 2016 May 13;3:153-157. doi: 10.1016/j.conctc.2016.05.007. eCollection 2016 Aug 15.
Randomized controlled trials (RCTs) are considered the most robust research design to determine the effectiveness of interventions. RCTs comparing surgery to non-surgical alternatives are particularly difficult to perform, partly due to difficulties with recruitment. Low recruitment rates can limit the internal and external validity of a trial thus understanding their causes may be important for avoiding protracted recruitment periods. This study aimed to report patient factors that influenced participation in a trial comparing surgery to a non-surgical treatment approach.
This study was a cross-sectional study nested within CROSSBAT (Combined Randomized and Observational Study of Surgery For Type B Ankle Fracture Treatment). Eligible participants willing to be randomized were randomized while those who declined randomization were offered participation in an observational cohort. Participants from both groups (randomized and observational) were asked to indicate their level of agreement on a 100 mm line with statements concerning reasons for acceptance or rejection of randomization. A subset were asked to state the primary reason for agreeing to participate or not in the trial.
The nested study included 312 participants; 113 who accepted and 199 who declined randomization. Participants unwilling to be randomized (those in the observational arm of the study) predominantly received a non-surgical intervention. They were significantly more worried about receiving treatment by chance (55 mm vs. 33 mm; p < 0.0001) and had a significantly higher preference for one particular treatment (less equipoise) (82 mm vs 43 mm; p < 0.0001) compared to participants willing to be randomized. Influence from clinicians and risk avoidance were primary influences of participation. Participants' responses regarding protocol burden, study follow-up requirements and altruism did not significantly differ between groups.
Patient non-participation in an RCT comparing surgery to no surgery is related to concern about receiving a treatment through chance and the presence of a strong preference for a particular treatment, particularly a non-surgical one. To avoid protracted recruitment periods, investigators can increase the number of study sites and ensure personnel involved have equipoise and are trained to provide a balanced view of both treatment arms.
随机对照试验(RCT)被认为是确定干预措施有效性的最可靠研究设计。比较手术与非手术替代方案的随机对照试验特别难以开展,部分原因是招募困难。低招募率会限制试验的内部和外部有效性,因此了解其原因对于避免冗长的招募期可能很重要。本研究旨在报告影响参与一项比较手术与非手术治疗方法试验的患者因素。
本研究是一项嵌套在CROSSBAT(B型踝关节骨折治疗的联合随机和观察性研究)中的横断面研究。愿意被随机分组的符合条件的参与者被随机分组,而拒绝随机分组的参与者被邀请参加观察性队列研究。两组(随机分组和观察性)的参与者被要求在一条100毫米的线上表明他们对关于接受或拒绝随机分组原因的陈述的同意程度。一部分参与者被要求说明同意或不同意参加试验的主要原因。
该嵌套研究包括312名参与者;113名接受随机分组,199名拒绝随机分组。不愿被随机分组的参与者(研究观察性队列中的参与者)主要接受非手术干预。与愿意被随机分组的参与者相比,他们更担心随机接受治疗(55毫米对33毫米;p<0.0001),并且对一种特定治疗的偏好明显更高( equipoise较低)(82毫米对43毫米;p<0.0001)。临床医生的影响和风险规避是参与的主要影响因素。两组参与者对方案负担、研究随访要求和利他主义的回答没有显著差异。
患者不参与比较手术与非手术的随机对照试验与担心随机接受治疗以及对特定治疗(特别是非手术治疗)有强烈偏好有关。为避免冗长的招募期,研究人员可以增加研究地点的数量,并确保相关人员保持equipoise,并接受培训以提供关于两种治疗方案的平衡观点。