Acceptance & Usability of an App Promoting Healthy Behaviours Amongst

Status Completed

Clinical Trial Summary

It is estimated that around 20% of breast cancers (BC) in the UK are preventable through adherence to appropriate health behaviours, i.e., healthy diet, physical activity, limited alcohol, not smoking, and that women at increased risk of BC could benefit from greater decreases in risk than the general population via health behaviour changes. Young women (age <35 years) who are at increased risk of developing BC currently receive little or no information regarding health behaviours and BC risk, or support for behaviour change. This feasibility study aims to explore whether a novel app is acceptable to women at increased risk and could potentially engage them with improved health behaviours which could reduce their future risk of BC.

Clinical Trial Description

Aims 1. To assess the acceptability and usability of the app to young women at increased risk of BC 2. To assess the feasibility of study procedures before running a future efficacy study using the app as an intervention Objectives 1. Explore views of users of the experiences during and after using the app 2. Explore views of users on their experience of the two different recruitment procedures (targeted mailshot, or social media, newsletters and websites), and the online consent procedure. 3. Interpret user data from the app including frequency and patterns of use of the different functions 4. Analyse recruitment data to explore how the two different recruitment procedures could be improved for the next study 5. Assemble a list of suggested changes to recruitment and consent procedures, and to the app, to be considered before the next study. 6. Quantify health care professional (HCP) time required for administering the private Facebook chat group, and through e-mail/private message support. 7. Quantify researcher time required for cleaning and analysis of app data. ;

Study Design

Related Conditions & MeSH terms

Clinical Trial Details

NCT number	NCT05460650
Study type	Interventional
Source	University of Manchester
Contact
Status	Completed
Phase	N/A
Start date	November 3, 2022
Completion date	March 10, 2023

View Details

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Clinical trials are conducted in a series of steps, called phases - each phase is designed to answer a separate research question.

Phase 1: Researchers test a new drug or treatment in a small group of people for the first time to evaluate its safety, determine a safe dosage range, and identify side effects.
Phase 2: The drug or treatment is given to a larger group of people to see if it is effective and to further evaluate its safety.
Phase 3: The drug or treatment is given to large groups of people to confirm its effectiveness, monitor side effects, compare it to commonly used treatments, and collect information that will allow the drug or treatment to be used safely.
Phase 4: Studies are done after the drug or treatment has been marketed to gather information on the drug's effect in various populations and any side effects associated with long-term use.

Acceptance and Usability of an App Promoting Healthy Behaviours Amongst Young Women at Increased Risk of Breast Cancer

Clinical Trial Summary

Clinical Trial Description

Study Design

Related Conditions & MeSH terms