Division of Endocrinology, Department of Medicine, University Health Network and University of Toronto, Toronto, Ontario, Canada.
Trials. 2010 Jul 26;11:81. doi: 10.1186/1745-6215-11-81.
Patients with early stage papillary thyroid carcinoma (PTC), are faced with the decision to either to accept or reject adjuvant radioactive iodine (RAI) treatment after thryroidectomy. This decision is often difficult because of conflicting reports of RAI treatment benefit and medical evidence uncertainty due to the lack of long-term randomized controlled trials.
We report the protocol for a parallel, 2-arm, randomized trial comparing an intervention group exposed to a computerized decision aid (DA) relative to a control group receiving usual care. The DA explains the options of adjuvant radioactive iodine or no adjuvant radioactive iodine, as well as associated potential benefits, risks, and follow-up implications. Potentially eligible adult PTC patient participants will include: English-speaking individuals who have had recent thyroidectomy, and whose primary tumor was 1 to 4 cm in diameter, with no known metastases to lymph nodes or distant sites, with no other worrisome features, and who have not received RAI treatment for thyroid cancer. We will measure the effect of the DA on the following patient outcomes: a) knowledge about PTC and RAI treatment, b) decisional conflict, c) decisional regret, d) client satisfaction with information received about RAI treatment, and e) the final decision to accept or reject adjuvant RAI treatment and rationale.
This trial will provide evidence of feasibility and efficacy of the use of a computerized DA in explaining complex issues relating to decision making about adjuvant RAI treatment in early stage PTC.
Clinical Trials.gov Identifier: NCT01083550.
患有早期甲状腺乳头状癌(PTC)的患者在甲状腺切除术后,面临着接受或拒绝辅助放射性碘(RAI)治疗的决定。由于缺乏长期随机对照试验,RAI 治疗获益的报告以及医学证据的不确定性存在冲突,因此该决定往往具有难度。
我们报告了一项平行、2 臂、随机试验的方案,该试验比较了接受计算机化决策辅助(DA)的干预组与接受常规护理的对照组。该 DA 解释了辅助放射性碘或不辅助放射性碘的选择,以及相关的潜在益处、风险和随访意义。潜在合格的成年 PTC 患者参与者将包括:最近接受甲状腺切除术的讲英语的个体,其原发性肿瘤直径为 1 至 4 厘米,无已知淋巴结或远处转移,无其他令人担忧的特征,并且尚未接受甲状腺癌的 RAI 治疗。我们将测量 DA 对以下患者结果的影响:a)对 PTC 和 RAI 治疗的了解,b)决策冲突,c)决策后悔,d)对 RAI 治疗信息的满意度,以及 e)接受或拒绝辅助 RAI 治疗的最终决定和理由。
该试验将为在解释有关早期 PTC 辅助 RAI 治疗决策的复杂问题中使用计算机化 DA 的可行性和功效提供证据。
ClinicalTrials.gov 标识符:NCT01083550。