Afiyanti Yati, Juliastuti Dyah, So Winnie Kwok Wei, Milanti Ariesta, Nasution Lina Anisa, Prawesti Aprilia Dian
Faculty of Nursing, Universitas Indonesia, Depok, Indonesia.
Program Study of Nursing, Faculty of Health Sciences, Universitas Ichsan Satya, South Tangerang, Indonesia.
PLoS One. 2024 Dec 18;19(12):e0299901. doi: 10.1371/journal.pone.0299901. eCollection 2024.
Most Indonesian gynecological cancer survivors have unmet supportive care needs during chemotherapy, which may lower their quality of life and discontinue the treatment. Digital health intervention can address this issue. This pilot investigation aims to (1) examine the feasibility and acceptability of a Fighting on distRess, Self-efficacy, Health Effects, and seXual issues (FoRSHE-X) intervention and (2) evaluate prospectively the impact of the study implementation on the level of distress, self-efficacy, side effects' knowledge and management, and sexual quality of life using the RE-AIM (Reach Effectiveness, Adoption, Implementation, and Maintenance) framework. This is a non-randomized mixed-methods pilot study. We will recruit women diagnosed with gynecological cancer undergoing chemotherapy to participate in the FoRSHE-X intervention consisting of ten weeks of social media-based education and telecoaching. We will evaluate the primary outcomes of study feasibility and acceptability, and the secondary outcomes of study impacts at three time points with quantitative and qualitative inquiries. We anticipate a minimum of 30 participants to enroll in the study and complete the assessment. We will disseminate results through conferences and peer-reviewed scientific journals. This study will imply whether a definitive trial to evaluate the potential benefits of the FoRSHE-X is viable and how it should proceed. The protocol can aid researchers or nurses in implementing this approach in their study or practice. Trial registration: Clinical trial registration number: ISRCTN13311651.
大多数印度尼西亚妇科癌症幸存者在化疗期间的支持性护理需求未得到满足,这可能会降低她们的生活质量并导致治疗中断。数字健康干预可以解决这一问题。这项试点调查旨在:(1)检验“应对压力、自我效能、健康影响及性问题”(FoRSHE-X)干预措施的可行性和可接受性;(2)使用RE-AIM(覆盖范围、有效性、采用率、实施情况及维持情况)框架,前瞻性评估该研究实施对痛苦程度、自我效能、副作用知识及管理以及性生活质量的影响。这是一项非随机混合方法试点研究。我们将招募被诊断患有妇科癌症且正在接受化疗的女性参与FoRSHE-X干预,该干预包括为期十周的基于社交媒体的教育和电话辅导。我们将通过定量和定性调查在三个时间点评估研究可行性和可接受性的主要结果以及研究影响的次要结果。我们预计至少有30名参与者登记参加该研究并完成评估。我们将通过会议和同行评审科学期刊传播研究结果。这项研究将表明评估FoRSHE-X潜在益处的确定性试验是否可行以及应如何进行。该方案可为研究人员或护士在其研究或实践中实施此方法提供帮助。试验注册:临床试验注册号:ISRCTN13311651。