A randomised controlled trial and consumer characteristics of the Mindful eHealth wellbeing program.

Authors
Category Primary study
Registry of TrialsANZCTR
Year 2014
INTERVENTION: A randomised controlled trial will be used to investigate the effectiveness of the Mindful eHealth program. The Mindful eHealth program is placed within the Federation eHealth Platform. People visiting the website, in response to advertisements or through self interest, will be informed of the availability of the Mindful eHealth program and invited to participate in the study. People taking part in the study will be randomly allocated to either an immediate access to the online program, or delayed assess (15 week delay). The Mindful eHealth program consists of three sessions designed to make an individual more mindful or being aware of moment‐to‐moment experiences (e.g., thoughts, feelings, images, sensations) and simply accepting what is there and not wanting it to change it in any way. Participants will spend a week on each session before moving onto the next session, so as to practise and to reinforce the session material learnt. Each session will last 15 minutes and its user friendly and interactive components are designed to keep the user engaged. To consolidate learning, participants will be given activities (five minutes per day) to complete offline to practise the principles of mindfulness and asked to provide simple feedback on this practise at the next session. Participants will also be sent automated emails (e.g., reminding them to log on (when they haven't for a period of time), when to complete questionnaires (with automated reminders when they are not completed in a timely manner), when new modules are released). Participants will complete online questionnaires at pre‐program, during‐program, post‐program, and at one and three month follow‐up stages of the study and will have access to the eHealth program for the duration of the study. CONDITION: Anxiety Depression Mental Wellbeing PRIMARY OUTCOME: Depressive symptoms via the Depression Scale using the DASS‐21. SECONDARY OUTCOME: Anxiety symptoms via the Anxiety Scale using the DASS‐21. Intervention Credibility using the Treatment Credibility Scale. Intervention Satisfaction using the Intervention Satisfaction Questionnaire. Perceived Stress ‐ using the Perceived Stress Scale. Psychological Distress using the Kessler‐6. Wellbeing using the Mental Health Continuum Short Form; Flourishing Scale; Personal Wellbeing Index; Mindfulness Attention Awareness Scale. INCLUSION CRITERIA: Participants must be 18 years or older, have access to the internet, provide consent and be able to register online using an email address.
Epistemonikos ID: 23d6efb2b8ed7b772ccd99b256a2d87b6140f966
First added on: Aug 22, 2024