College of Nursing, Rady Faculty of Health Sciences, University of Manitoba, Winnipeg, MB, Canada.
Research Institute in Oncology and Hematology, CancerCare Manitoba, Winnipeg, MB, Canada.
Support Care Cancer. 2021 Oct;29(10):5681-5690. doi: 10.1007/s00520-021-06038-7. Epub 2021 Feb 17.
We aimed to determine the impact of a primary treatment consultation recording on perception of being informed, satisfaction with cancer care, satisfaction with the oncologist, and psychological distress in patients with brain tumors.
This was a prospective, double-blind, parallel, randomized controlled trial conducted in 3 Canadian cities, in which patients who had their initial treatment consultation recorded were assigned to either receive their digital recording or not. It was hypothesized that patients who received their recording would realize statistically significant benefit on the outcomes of interest at 1 week, 3 months, and 6 months post-consultation in comparison to patients who did not receive their recording. Outcome measures included the following: Patient Satisfaction with Cancer Scale, Hospital Anxiety and Depression Scale, PrestMan Satisfaction with Doctor Scale, and Perception of Being Informed Scale.
Of the 246 eligible patients, 133 participated (60.9% male; age M=52.4 years; 53.4% grade IV disease). Of these, 63 received their consultation recording and 70 did not. Intention-to-treat analysis showed that, compared to baseline, patients who received their consultation recording reported being more fully informed about their disease and treatment at 1 week post-consultation than patients who did not receive their recording (p = 0.007), but this finding was no longer significant at 3 and 6 months. There were no statistically significant differences observed between the two groups on the measures of satisfaction with cancer care, satisfaction with the doctor, and depression or anxiety at any assessment time point, though the study was under-powered.
The study findings show that primary treatment consultation recordings may provide limited benefit beyond brain tumor patients' perception of being informed, despite being highly valued by these patients, and high listening rates among their significant others. The lack of statistical power should be considered when interpreting the findings.
ClinicalTrials.gov - NCT01866228.
我们旨在确定主要治疗咨询记录对脑瘤患者的知情感知、癌症护理满意度、对肿瘤医生的满意度和心理困扰的影响。
这是一项在加拿大 3 个城市进行的前瞻性、双盲、平行、随机对照试验,其中对接受初始治疗咨询记录的患者进行了记录或不记录的分配。假设与未接受记录的患者相比,接受记录的患者在咨询后 1 周、3 个月和 6 个月时对感兴趣的结局会有统计学上显著的获益。结果衡量指标包括:癌症患者满意度量表、医院焦虑抑郁量表、PrestMan 医生满意度量表和知情感知量表。
在 246 名符合条件的患者中,有 133 名患者参与(60.9%为男性;年龄 M=52.4 岁;53.4%为 IV 级疾病)。其中,63 名患者接受了咨询记录,70 名患者未接受。意向治疗分析显示,与基线相比,接受咨询记录的患者在咨询后 1 周时报告对自己的疾病和治疗有了更全面的了解,而未接受记录的患者则没有(p=0.007),但这一发现在 3 个月和 6 个月时不再显著。在任何评估时间点,两组在癌症护理满意度、对医生的满意度以及抑郁或焦虑的测量上均无统计学差异,尽管该研究的效力不足。
尽管这些患者高度重视咨询记录并具有较高的听取率,但研究结果表明,主要治疗咨询记录可能仅提供有限的益处,除了脑瘤患者的知情感知之外,尽管这些记录深受这些患者的重视。在解释研究结果时,应考虑到统计效力不足的问题。
ClinicalTrials.gov - NCT01866228。