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Набор скоро начнётся NCT07640698

TELESM-edu.Nursing: a Personalised Nursing Intervention for People With Multiple Sclerosis

Без фазы С лечением Multiple Sclerosis (MS) Telenursing

Ориентир для пациента и семьи

Простыми словами

Автоматическая сводка по структурированным данным реестра. Она помогает сориентироваться, но не заменяет официальный протокол или оценку врача.

Что изучают
В протоколе указаны: TELESM-edu.nursing, Standard.
Кому может быть актуально
Состояния в реестре: Multiple Sclerosis (MS), Telenursing. Базовые параметры: от 18 лет · Все.
Что важно проверить
Возраст, диагноз и пол — только базовые ориентиры. Предыдущее лечение, анализы и другие обязательные условия указаны ниже в критериях участия.
Где проводится
Список центров уточняется — проверьте первичный протокол.
Следующий шаг
Сохраните исследование, покажите его лечащему врачу и уточните актуальный статус у исследовательского центра. Расходы, документы и поездка →
Официальное название

TELESM-edu.Nursing: Efficacy of a Personalised Nursing Intervention for the Management of People With Multiple Sclerosis

Обзор

The primary aim of this study is to evaluate the impact of the telenursing intervention "TELESM-edu.nursing" on people with Multiple Sclerosis (pwMS), specifically focusing on their navigational capacity within the healthcare system (Navigation Health Literacy) and their perceived level of Health Literacy. The study will also assess the effectiveness of the intervention in improving patient satisfaction with current therapy, patients' beliefs and attitudes towards the prescribed therapeutic regimen, satisfaction of informational needs, trust in nurses, and degree of disability. The secondary objective is to evaluate the feasibility and sustainability of a personalised telenursing programme for pwMS. Feasibility will be assessed based on: (I) the ability to recruit and retain participants, measured through adherence rates and dropout rates in the intervention group; (II) participants' acceptability, usability, and satisfaction with the intervention; and (III) healthcare staff satisfaction and perceived usability of the intervention. The main research questions addressed in this study are: Does the "TELESM-edu.nursing" intervention improve patients' Navigation Health Literacy and overall Health Literacy levels? Does the intervention improve patient satisfaction with therapy and fulfilment of informational needs? Does the intervention positively influence patients' beliefs and attitudes towards their treatment? Does the intervention increase trust in nurses? What is the impact of the intervention on patients' level of disability? Is the telenursing programme feasible, acceptable, and sustainable for both patients and healthcare professionals? Both study groups will receive the standard in-person informational and educational programme, as well as routine follow-up visits according to the established care pathway. Participants assigned to the intervention group will additionally receive a personalised educational programme lasting six months. This programme will be delivered monthly by a nurse through educational video pills and nurse-led teleconsultations. Participants will be required to watch the video pills and take part in teleconsultations.

Вмешательства

  • Другое TELESM-edu.nursing
    The teleconsultation intervention will be tailored according to participants' health literacy (HL) levels, adapting content complexity, information load, language, interaction style, and methods to verify understanding, while maintaining consistent participation goals. For patients with low HL, the intervention will focus on simplifying and progressively structuring information, prioritising essential and practical content. Understanding will be assessed using teach-back and Teach-to-Goal strat
  • Другое Standard
    The standard informational and educational programme provides that the physician and the health professionals involved in the care pathway, in particular the nurse, furnish patients taken care of at the Centre with information regarding the disease, the therapeutic and care pathway, and the management of the clinical condition. The standard intervention includes education on informed selection of information sources relevant to patients' areas of interest, and the clarification of any questions

Первичные конечные точки

  • Change in Navigational Health Literacy (Ability to Navigate Health Systems and Services) Assessed by the HLS19-NAV Instrument From Baseline to 6-Month Follow-up [Срок оценки: Assessed at baseline, 3 months, and at the 6-month final follow-up.]
  • Change in Health Literacy Level Assessed by the Single-Item Literacy Screener (SILS) From Baseline to 6-Month Follow-up [Срок оценки: Assessed at baseline, 3 months, and at the 6-month final follow-up.]
  • Change in Patient Satisfaction With Current Therapy Assessed by a Single-Item Satisfaction Measure From Baseline to 6-Month Follow-up [Срок оценки: Assessed at baseline and at the 6-month final follow-up.]
  • Change in Beliefs About the Necessity of Prescribed Medicines Assessed by the Beliefs about Medicines Questionnaire-Specific (BMQ-Specific) Necessity Subscale From Baseline to 6-Month Follow-up [Срок оценки: Assessed at baseline and at the 6-month final follow-up.]
  • Change in Concerns About Prescribed Medicines Assessed by the Beliefs about Medicines Questionnaire-Specific (BMQ-Specific) Concerns Subscale From Baseline to 6-Month Follow-up [Срок оценки: Assessed at baseline and at the 6-month final follow-up.]
  • Change in Trust in Nurses Assessed by the Trust in Nurses Scale (TNS) From Baseline to 6-Month Follow-up [Срок оценки: Assessed at baseline, 3 months, and at the 6-month final follow-up.]
  • Satisfaction of Patients' Informational Needs at 6-Month Follow-up [Срок оценки: Assessed at the 6-month final follow-up.]
  • Change in Disability Level Assessed by the Expanded Disability Status Scale (EDSS) From Baseline to 6-Month Follow-up [Срок оценки: Assessed at baseline and at the 6-month final follow-up.]
Вторичные конечные точки (6)
  • Feasibility of the TELESM-edu.nursing Programme Assessed by Participant Retention and Adherence Rates Over the 6-Month Study Period [Срок оценки: Assessed at 3 months and at the 6-month final follow-up.]
  • Acceptability of the TELESM-edu.nursing Intervention Assessed by a TFA-Based Questionnaire at 6-Month Follow-up [Срок оценки: Assessed at the 6-month final follow-up.]
  • Usability of the TELESM-edu.nursing Intervention Assessed by a Single-Item Measure at 6-Month Follow-up [Срок оценки: Assessed at the 6-month final follow-up.]
  • Satisfaction With the TELESM-edu.nursing Intervention Assessed by a Single-Item Measure at 6-Month Follow-up [Срок оценки: Assessed at the 6-month final follow-up.]
  • Staff Satisfaction With the TELESM-edu.nursing Intervention Assessed Through Semi-Structured Interviews at 6-Month Follow-up [Срок оценки: Assessed at the 6-month final follow-up.]
  • Staff-Perceived Usability of the TELESM-edu.nursing Intervention Assessed Through Semi-Structured Interviews at 6-Month Follow-up [Срок оценки: Assessed at the 6-month final follow-up.]

Критерии участия

Критерии включения

  • Patients of both sexes (male and female)
  • Age 18 years or older
  • Confirmed diagnosis of relapsing-remitting multiple sclerosis (RRMS), primary progressive multiple sclerosis (PPMS), or secondary progressive multiple sclerosis (SPMS)
  • Currently receiving pharmacological treatment for multiple sclerosis
  • Expanded Disability Status Scale (EDSS) score of 7.5 or lower
  • Ability to read and understand Italian
  • Ability to provide written informed consent
  • Access to a suitable device (smartphone, tablet, or computer with a webcam)
  • Access to a home internet connection

Критерии исключения

  • Age younger than 18 years
  • Expanded Disability Status Scale (EDSS) score higher than 7.5
  • Presence of psychiatric disorders that may interfere with participation in the study
  • Presence of cognitive impairment that may interfere with participation in the study

Критерии приведены из реестра в оригинале (на английском). Окончательную оценку соответствия проводит исследовательский центр.

Здоровые добровольцы: Нет

Дизайн исследования

Распределение
Рандомизированное
Модель
Параллельные группы
Маскирование
Простое слепое
Основная цель
Поддерживающая терапия

Центры проведения

Список центров уточняется — проверьте первичный протокол.

Идентификаторы

NCT: NCT07640698 · TELESM1

Первоисточники (государственные реестры)

Открыть это исследование на ClinicalTrials.gov ↗