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临床试验/NCT05839223
NCT05839223已完成不适用

Clinical Pharmacist Role in Increasing the Adherence to Recommendations Among Patients Using Isotretinoin: A Randomized, Controlled Study

Jordan University of Science and Technology2 个研究点 分布在 1 个国家目标入组 207 人开始时间: 2020年9月1日最近更新:
适应症

试验速览

阶段
不适用
状态
已完成
入组人数
207
试验地点
2
主要终点
Knowledge

研究概览

简要总结

The objective of the study was to evaluate the role of clinical pharmacists in improving adherence to medication and the recommendations related to isotretinoin, awareness about proper use, dealing with the side effects, and anxiety and depressive symptoms. Patients were randomly assigned to an intervention group (received the educational process (recommendations) about isotretinoin by a clinical pharmacist in addition to the routine education about isotretinoin provided by the physician) and a control group (received only the routine education about isotretinoin provided by the physician) and then followed for three months. Patient's adherence to the recommendations, patient's knowledge about isotretinoin, and side effects management for both groups were measured through a set of questions adapted from a validated questionnaire at baseline and after three months. Adherence scale was used to evaluate adherence to the medication after three months. Hospital Anxiety and Depression Scale were used to assess depressive and anxiety symptoms at baseline and at follow-up in each group.

详细描述

Patients and Settings

Patients who attended dermatological clinics (at King Abdullah University Hospital (KAUH), Princess Basma Hospital (PBH), and Prince Rashid Hospital (PRH). The study was conducted over the period from September/2020 to February/2021) to receive isotretinoin medication, with any brand names known in Jordan like (ISOSUPRA®, ROACCUTANE®, CURANCE®, RUATINE®,) and met the inclusion criteria were approached and asked to participate in the study. The following are the inclusion criteria:

  • Male or female patients aged 18 years or older who were using isotretinoin.
  • Patients with a current diagnosis of moderate to severe acne vulgaris.
  • Patients who were on or going to receive standard isotretinoin doses (0.5-1mg/kg/day).
  • Patients who were willing to participate in the study and to do a follow-up.

Patients with any contraindication to isotretinoin who cannot take the medication and patients who were not willing to participate in the study were excluded as explained in the following:

  • Pregnant women and women who intend to become pregnant.
  • Breastfeeding women.
  • Presence of any renal or hepatic compromise or any pre-existing hyperlipidemia.

研究设计

研究类型
Interventional
分配方式
Randomized
干预模型
Parallel
主要目的
Other
盲法
Double (Participant, Care Provider)

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

  • Male or female patients aged 18 years or older who were using isotretinoin.
  • Patients with a current diagnosis of moderate to severe acne vulgaris.
  • Patients who were on or going to receive standard isotretinoin doses (0.5-1mg/kg/day).
  • Patients who were willing to participate in the study and to do a follow-up.

排除标准

  • Pregnant women and women who intend to become pregnant.
  • Breastfeeding women.
  • Presence of any renal or hepatic compromise or any pre-existing hyperlipidemia.
  • Patients who were not willing to participate in the study.

结局指标

主要结局

Knowledge

时间窗: 3 months

The patient knowledge section consisted of ten different questions/items, and each item had two answers (yes/no). Items were coded according to the answer; the correct (adequate) answer was coded as one (1), while the wrong (not adequate) answer was coded as zero (0). So, the knowledge score could take the values of 0 (no knowledge) to 10 (perfect knowledge).

Adherence to the Recommendations

时间窗: 3 months

10 items for all patients, and each item had answers (yes/no). Items were coded according to the answer; the correct (adherent) answer was coded as one (1), while the wrong (not adherent) answer was coded as zero (0). The adherence score of patients 'compliance with the recommendations ranged between 0 (least adherent) to 10 (most adherent).

次要结局

  • HADS(3 MONTHS)

研究者

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

Bushra Mahmoud Ahmad Hijazi

Assistant Professor

Jordan University of Science and Technology

研究点 (2)

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