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临床试验/NCT07664683
NCT07664683招募中不适用

Impact of Changing the Appearance of Oral Antineoplastics on Adherence and Continuity of Treatment, Patient-reported Health Outcomes, and Patient Experience of Care

Universidad Miguel Hernandez de Elche1 个研究点 分布在 1 个国家目标入组 334 人开始时间: 2025年12月8日最近更新:
适应症

试验速览

阶段
不适用
状态
招募中
入组人数
334
试验地点
1

研究概览

简要总结

Oral chemotherapy is a convenient and flexible option for cancer treatment that can improve patients quality of life and increase adherence to treatment compared to traditional intravenous chemotherapy. However, since patients are responsible for taking the medication, there can be issues with continuity and adherence. Like other medications, generics of existing oral chemotherapy have emerged, which help reduce costs and improve access to this therapy. These generics contribute to a more sustainable healthcare system, so it is necessary to implement effective strategies for their adoption.

Although generic treatments have been shown to be just as effective as the original drug, there is no regulation requiring the pill to have the same shape and color as the original (what we refer to as appearance). Additionally, the packaging of the treatment is different as it is specific to each brand. Therefore, a patient on a specific treatment may switch from the original medication to a generic or from one generic to another, which may have a different appearance in both the pill and the packaging.

It has been observed that these changes can lead to medication errors or a loss of patient confidence, resulting in decreased continuity and adherence to treatment. These issues have been seen with other medications for chronic diseases but have not been studied in cancer patients to date. In these patients, despite the nature of the disease suggesting they would be adherent to treatment, previous studies have shown that this is not the case, with only about 70% of patients being adherent. This lack of adherence affects treatment efficacy, increases the risk of disease relapse, and therefore negatively impacts patient s quality of life and survival while also increasing costs.

Therefore, this study focuses on evaluating whether these changes in pill appearance and/or packaging impact treatment continuity and adherence, as well as other relevant patient outcomes and their experience with the healthcare received. Additionally, we want to analyze whether there are patient variables (such as health literacy, age, or clinical variables) that influence the impact of these changes. Given the differences in adherence between men and women, it is essential to conduct these analyses separately for both genders.

The results obtained from this study will contribute to the development of educational strategies for managing oral chemotherapy by patients and healthcare professionals. Additionally, new evidence will be generated to allow decision-makers to establish policies, either by choosing treatments with the least change in appearance or by regulating the appearance of treatments. All of this will contribute to greater treatment effectiveness, improved patient quality of life, and a lower rate of disease recurrence.

详细描述

The project "APAR-AdhNEO" aims to evaluate the impact of a change in appearance (changes in shape and/or color of the tablet and/or packaging) of the prescribed oral antineoplastic (ANEO) (whether switching from brand-name to generic or between generics) on the patient's healthcare experience, treatment continuity and adherence, as well as patient-reported outcomes, and whether this differs between men and women.

Study Design Specifications The study follows a mixed-methods design. For secondary outcome 1 (secondary outcomes described in outcomes measure section), a prospective study will be designed to evaluate the frequency of changes in ANEO prescriptions. For secondary outcomes 2-5, a before-and-after study will be conducted to assess the impact of medication changes on various variables.

As part of the study evaluating the patient s experience with healthcare (secondary outcome 2), in addition to quantitatively assessing this experience before and after the change, a qualitative study will be conducted using focus groups with patients.

Sample Size Estimation According to a systematic review conducted by the research team, the frequency of non-adherence and/or treatment discontinuation after a change in appearance and/or packaging varies across studies. For example, a change in appearance was associated with a reduction in adherence to antihypertensive treatment (from 69% to 50%), preventive treatment for heart attacks (from 97% to 87%), and olanzapine treatment (from 28% to 16.7%), Another study on antidiabetics showed that the number of patients who discontinued their treatment after a medication change increased from 62% to 72%.

Moreover, a previous study conducted by the research team showed that adherence to ANEO treatment, evaluated using the EXPAD-ANEO scale and pill counting, was 69.3%.

研究设计

研究类型
Observational
观察模型
Cohort
时间视角
Other

入排标准

年龄范围
18 Years 至 —(Adult, Older Adult)
性别
All
接受健康志愿者

入选标准

  • Objective 1:
  • Inclusion criteria:
  • ANEOs included in the pharmacotherapeutic guide of the three hospitals for two years of follow-up (June 2025-2027) will be included.
  • Objectives 2-5:
  • Inclusion criteria:
  • Patients on treatment for at least 6 months with one of the following ANEOs will be included: capecitabine (L01BC06) (not used as adjuvant in short cycles), imatinib (L01EA01), everolimus (L04AA18), abiraterone (L02BX03) and lenalidomide (L04AX04), at the time of a change in their usual treatment (from brand to generic or between two generics).
  • Patients on treatment with ANEOs who meet the established criteria and who change their treatment from brand to generic or from one generic to another generic during the study period may also be included.

排除标准

  • Individuals who collect medication for others and those who are institutionalised will be excluded.
  • Patients who have been admitted to hospital in the last 4 weeks are also excluded, due to the increased control of their medication.
  • Objective 2( Qualitative analysis)
  • - Spanish Patient Forum

研究者

申办方类型
Other
责任方
Principal Investigator
主要研究者

Elsa López Pintor

Senior Lecturer in Pharmacy

Universidad Miguel Hernandez de Elche

研究点 (1)

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