Меню
Идёт набор NCT07051005

Feasibility of a Tailored Online Self-compassion Intervention

Без фазы С лечением Type 1 Diabetes Mellitus Type 2 Diabetes Mellitus (T2DM)

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: Feasibility RCT of a tailored online self-compassion intervention.
Кому может быть актуально
Состояния в реестре: Type 1 Diabetes Mellitus, Type 2 Diabetes Mellitus (T2DM). Базовые параметры: 18 лет — 99 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
Великобритания
Следующий шаг
Сохраните исследование, покажите его лечащему врачу и уточните актуальный статус у исследовательского центра. Расходы, документы и поездка →
Официальное название

A Feasibility Randomised Controlled Trial of Online Self-compassion Training Tailored for Adults Living With Type 1 and Type 2 Diabetes Mellitus

Обзор

The goal of this clinical trial is to examine the feasibility and acceptability of an online programme that is based on Compassionate Mind Training (CMT) over four-weeks. The programme intends to share information and strategies to reduce diabetes distress, self-criticism, and shame, and improve physical health in people who have Type 1 and Type 2 Diabetes Mellitus.

Подробное описание

This pilot randomised controlled trial seeks to examine the feasibility and acceptability of online compassion training tailored for adults living with Type 1 and Type 2 diabetes. Participants will be randomised to either the compassion training course or a waitlist control group, in which participants will be offered the intervention at the end of the study. Four self-report measures will be administered online at baseline (weeks 0-1) and post-intervention (weeks 9-10). The indices of feasibility and acceptability that will be examined include: 1. ease of recruitment; 2. participant retention in the intervention; 3. participant retention in the study; 4. acceptability of the intervention; 5. outcome measure completion; 6. whether there is a preliminary signal of efficacy on the primary outcome measure (diabetes distress). These indices will be compared to progression criteria which determine whether the intervention is sufficiently feasible and acceptable to progress to a full-scale RCT in future research.

Вмешательства

  • Поведенческое Feasibility RCT of a tailored online self-compassion intervention
    This is a four-week online self-compassion course supplied by Balanced Minds. The researches of this study and an Expert by Experience have consulted with the owner of Balanced Minds to tailor this programme to people with diabetes. The self-help, self-compassion course is based on Compassionate Mind Training. This provides participants with opportunities to develop skills and attributes of compassion through a weekly 30-minute video on a specified topic, a 10-minute compassionate exercise that

Первичные конечные точки

  • Number of participants recruited [Срок оценки: 6 months following the start of recruitment]
  • Proportion of intervention group participants who complete at least half of the compassion training course intervention sessions [Срок оценки: Weeks 2 to 8]
  • Proportion of study participants who remain in the study [Срок оценки: Weeks 0 to 10]
  • Compassion training course acceptability [Срок оценки: Weeks 9 to 10]
  • Completion rate of the outcome measures [Срок оценки: Weeks 0 to 10]
  • Estimate of between group effect size of the compassion training course intervention compared to control on the primary outcome measure of change in Diabetes Distress Scale scores from baseline (weeks 0-1) to post-intervention (weeks 9 - 10). [Срок оценки: Weeks 9 - 10]
Вторичные конечные точки (3)
  • Estimate of the between group effect size of compassion training intervention compared to control on change in the Forms of Self-Criticising/ Attacking & Self-Reassuring (FSCRS) Scale from baseline (weeks 0-1) to post-intervention (weeks 9-10). [Срок оценки: Weeks 9-10]
  • Estimate of the between group effect size of compassion training intervention compared to control on change in the External and Internal Shame Scale (EISS) from baseline (weeks 0-1) to post-intervention (weeks 9-10). [Срок оценки: Weeks 9-10]
  • Estimate of the between group effect size of compassion training intervention compared to control on change in the Compassionate Engagement and Action Scale (CEAS) from baseline (weeks 0-1) to post-intervention (weeks 9-10). [Срок оценки: Weeks 9-10]

Критерии участия

Критерии включения

  • 18 years old or older.
  • Diagnosed with Type 1 or Type 2 diabetes by a clinician in the NHS more than one year ago.
  • Self-managing theircondition.
  • Identified by their NHS team as needing support with their mental health due to diabetes-related distress.

Критерии исключения

  • <18
  • Individuals experiencing a current mental health crisis, including severe depression, active suicidal thoughts, or acute psychosis
  • Unable to read/speak English
  • Gestational diabetes, Wolfram, and other rarer conditions
  • Individuals currently experiencing severe substance abuse issues that could interfere with participation in the programme
  • Individuals without reliable access to the internet and a compatible device (computer or smartphone).

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

Великобритания · 2 центра
  • Betsi Cadwaladr University Health Board (BCUHB) — Bangor
  • Barts Health NHS Trust — London

Публикации

  • Banks J, Amspoker AB, Vaughan EM, Woodard L, Naik AD. Ascertainment of Minimal Clinically Important Differences in the Diabetes Distress Scale-17: A Secondary Analysis of a Randomized Clinical Trial. JAMA Netw Open. 2023 Nov 1;6(11):e2342950. doi: 10.1001/jamanetworkopen.2023.42950. PMID 37966840

Идентификаторы

NCT: NCT07051005 · ETH2425-0223

Первоисточники (государственные реестры)

Открыть это исследование на ClinicalTrials.gov ↗