Hu S, Guinan E, Mockler D, O'Neill L
School of Pharmacy and Pharmaceutical Sciences, Trinity College Dublin, University of Dublin, Dublin 8, Ireland.
Trinity St. James's Cancer Institute, Dublin, Ireland.
J Cancer Surviv. 2024 Apr 3. doi: 10.1007/s11764-024-01569-4.
Retention is a key marker of trial success. Poor retention can induce bias, reduce statistical power and minimise the validity of trials. This review examined retention rates in exercise trials in cancer survivors, reasons for non-retention and retention strategies utilised.
A systematic review was conducted using a predefined search strategy in EMBASE RCTs, MEDLINE OVID, CINAHL, Web of Science-Core Collection and Cochrane Central Register of Controlled Trials (CENTRAL). The search was conducted on 27/03/2023. Title and abstract screening, full text review and data extraction were completed in duplicate.
Of 17,524 studies identified, 67 trials involving 6093 participants were included. The median overall retention rate immediately post-intervention was 89.85%, range (52.94-100%) and mean 87.36% (standard deviation 9.89%). Trials involving colorectal cancer survivors only had the highest median retention rate (94.61%), followed by breast (92.74%), prostate (86.00%) and haematological cancers (85.49%). Studies involving mixed cancer cohorts had the lowest retention rate (80.18%). The most common retention strategies were wait-list control groups, regular check-ins/reminders and free exercise equipment. Common reasons for non-retention were lost to follow-up, health problems, personal reasons including family/work commitments and travel burden, and disease progression.
Retention rates in exercise oncology trials are approximately 90% immediately post-interventions. Our previous work highlighted variable suboptimal recruitment rates of median 38% (range 0.52-100%). Recruitment rather than retention should be prioritised for methodology research in exercise oncology.
Optimising the quality of exercise oncology trials is critical to informing high quality survivorship care. PROSPERO registration number: CRD42023421359.
留存率是试验成功的关键指标。留存率低会导致偏差、降低统计效力并使试验的有效性降至最低。本综述考察了癌症幸存者运动试验中的留存率、未留存的原因以及所采用的留存策略。
采用预定义的检索策略在EMBASE随机对照试验、MEDLINE OVID、护理学与健康领域数据库、科学网核心合集以及Cochrane对照试验中心注册库(CENTRAL)中进行系统综述。检索于2023年3月27日进行。标题和摘要筛选、全文审查以及数据提取均重复进行。
在检索到的17524项研究中,纳入了67项试验,涉及6093名参与者。干预后立即的总体留存率中位数为89.85%,范围为(52.94 - 100%),均值为87.36%(标准差9.89%)。仅涉及结直肠癌幸存者的试验留存率中位数最高(94.61%),其次是乳腺癌(92.74%)、前列腺癌(86.00%)和血液系统癌症(85.49%)。涉及多种癌症队列的研究留存率最低(80.18%)。最常见的留存策略是候补对照组、定期检查/提醒以及免费运动设备。未留存的常见原因是失访、健康问题、包括家庭/工作事务和出行负担在内的个人原因以及疾病进展。
运动肿瘤学试验干预后立即的留存率约为90%。我们之前的工作强调了招募率参差不齐且不理想,中位数为38%(范围0.52 - 100%)。在运动肿瘤学的方法学研究中,应优先考虑招募而非留存。
优化运动肿瘤学试验的质量对于提供高质量的生存护理至关重要。国际前瞻性系统评价注册库注册号:CRD42023421359。