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NCT05891431

Engagement and Acceptability of the Untire mHealth App

Active, enrolled NA Last updated 19 September 2024
What this trial tests

NA trial testing Untire mobile app in Cancer-related Problem/Condition in 34 participants. Participants enrolled and being followed up; not accepting new ones.

Timeline
15 December 2023
Primary endpoint
16 September 2024
1 October 2025

Quick facts

Lead sponsorUniversity of Bath
PhaseNA
StatusActive, enrolled
Study typeINTERVENTIONAL
Allocationna
Designsingle group
Maskingnone
Primary purposetreatment
Enrollment34
Start date15 December 2023
Primary completion16 September 2024
Estimated completion1 October 2025
Sites2 locations across United Kingdom

Drugs / interventions tested

Conditions studied

Sponsor

University of Bath

Who can join

18 and older, any sex, with Cancer-related Problem/Condition or Cancer-related Fatigue. Patients with the condition only — healthy volunteers not accepted.

Sponsor's own description

The aim of this study will be to assess the engagement and acceptability of the Untire mHealth intervention for adults with cancer related fatigue. Acceptability will be assessed after 2, 4, 6 and 12 weeks of app use. Participants (both those competed the study and those who stopped using the app) will be asked about their engagement with the app. A secondary aim of this study will be to provide preliminary efficacy outcomes of the Untire intervention in reducing fatigue and QoL in adults experiencing cancer related fatigue.

Publications & conference data

No peer-reviewed publications indexed yet for this trial.

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Other recruiting trials for Cancer-related Problem/Condition

Currently open trials in the same condition.

Other University of Bath trials

Trials by the same sponsor.

Verify against primary sources

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/NCT05891431.

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