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NCT04287296

A 12-week Feasibility Trial of a Mental Health Breakfast Show Wakey

Completed NA Last updated 23 February 2021
What this trial tests

NA trial testing Wakey! in Mental Wellbeing in 3,993 participants. Completed in 21 May 2020.

Timeline
20 January 2020
Primary endpoint
10 April 2020
21 May 2020

Quick facts

Lead sponsorMethod X Studios Ltd
PhaseNA
StatusCompleted
Study typeINTERVENTIONAL
Allocationna
Designsingle group
Maskingnone
Primary purposeprevention
Enrollment3,993
Start date20 January 2020
Primary completion10 April 2020
Estimated completion21 May 2020
Sites1 location across United Kingdom

Drugs / interventions tested

Conditions studied

Sponsor

Method X Studios Ltd

Who can join

18 and older, any sex, with Mental Wellbeing. Patients with the condition only — healthy volunteers not accepted.

Sponsor's own description

The aim of Wakey! is to increase access to wellbeing support to lower socio-economic groups who have traditionally been excluded from the design and evaluation of digital mental health interventions. This feasibility study is designed to explore engagement, initial efficacy and experience of using Wakey! in the underserved populations in the United Kingdom. This will be used to further adapt and refine the intervention, so it is appealing and effective in the target populations.

Publications & conference data

1 peer-reviewed publication reference this trial (live from Europe PMC):

  1. Improving Access to Behavioral Strategies to Improve Mental Well-being With an Entertaining Breakfast Show App: Feasibility Evaluation Study.
    Öeren M, Jordan I, Coughlin D, Turnbull S. · · 2022 · cited 1× · PMID 35319468 · DOI 10.2196/25715

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Other recruiting trials for Mental Wellbeing

Currently open trials in the same condition.

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Data sources for this page

Drug Landscape aggregates and links these public records for informational use only. Always verify against the primary source before clinical or regulatory decisions. Canonical URL: https://druglandscape.com/trial/NCT04287296.

Primary sources · FDA · ClinicalTrials.gov · EMA · SEC EDGAR · ChEMBL · Wikidata · full sourcing