Evaluation of a 5-a-day Fruit and Vegetable Mobile Phone Application

NCT ID: NCT02779491

Last Updated: 2019-10-08

Study Results

Results available

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Basic Information

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Recruitment Status

COMPLETED

Clinical Phase

NA

Total Enrollment

94 participants

Study Classification

INTERVENTIONAL

Study Start Date

2016-06-01

Study Completion Date

2018-12-30

Brief Summary

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This is a randomized controlled trial to assess the impact of a novel fruit and vegetable mobile phone application on fruit and vegetable intakes, knowledge and attitudes.

Detailed Description

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The 5-a-day fruit and vegetable (FV) message from the WHO recommends consumption of five 80g portions of different FV per day for health reasons. Recent research suggests that the details of the message are poorly understood by the population as a whole, by low consumers of FV and by those in demographic groups of traditional low FV consumption, and that this poor knowledge impacts on implementation of the message to result in low FV intakes. To aid implementation of the recommendations, investigators have developed a 5-a-day FV mobile phone application (app) prototype. The basic prototype app will provide information on the 5-a-day message, allow users to input consumption, and provides consumers with accurate knowledge of their adherence to the recommendations. This study will investigate the use and impact of the prototype app on FV intakes over a two or four week period. For significant impacts on health, sustained user engagement and use will be required. Up to 100 participants will be randomised to either receive or not receive the app, and will be asked to use the app for the following two or four weeks. FV intake will be assessed at baseline, 2 weeks, 4 weeks. Measures of app use will also be taken at these time points. Measures of FV knowledge will also be measured at these time points. Measures of FV attitudes were initially planned but not undertaken to reduce demand characteristics for participants. The investigators anticipate that changes in intakes will be mediated by changes in knowledge and attitudes.

Conditions

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Nutritional Status Nutrition Assessment

Study Design

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Allocation Method

RANDOMIZED

Intervention Model

PARALLEL

Primary Study Purpose

PREVENTION

Blinding Strategy

SINGLE

Outcome Assessors

Study Groups

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Intervention for two weeks

Receipt of the mobile phone application for two weeks

Group Type EXPERIMENTAL

5-a-day fruit and vegetable mobile phone application

Intervention Type BEHAVIORAL

5-a-day fruit and vegetable mobile phone application

Control for two weeks

Usual habitual activity - no receipt of mobile phone application for two weeks

Group Type NO_INTERVENTION

No interventions assigned to this group

Intervention for four weeks

Receipt of the mobile phone application for four weeks

Group Type EXPERIMENTAL

5-a-day fruit and vegetable mobile phone application

Intervention Type BEHAVIORAL

5-a-day fruit and vegetable mobile phone application

Control for four weeks

Usual habitual activity - no receipt of mobile phone application for two weeks

Group Type NO_INTERVENTION

No interventions assigned to this group

Interventions

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5-a-day fruit and vegetable mobile phone application

5-a-day fruit and vegetable mobile phone application

Intervention Type BEHAVIORAL

Eligibility Criteria

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Inclusion Criteria

* able to provide informed consent
* speaks English, owns an android mobile telephone
* able and willing to use phone and complete all measures

Exclusion Criteria

* none
Minimum Eligible Age

18 Years

Eligible Sex

ALL

Accepts Healthy Volunteers

Yes

Sponsors

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Bournemouth University

OTHER

Sponsor Role lead

Responsible Party

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Responsibility Role SPONSOR

References

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Appleton KM, Passmore D, Burn I, Pidgeon H, Nation P, Boobyer C, Jiang N. An Interactive Mobile Phone App (SMART 5-A-DAY) for Increasing Knowledge of and Adherence to Fruit and Vegetable Recommendations: Development and Pilot Randomized Controlled Trial. JMIR Mhealth Uhealth. 2019 Nov 20;7(11):e14380. doi: 10.2196/14380.

Reference Type DERIVED
PMID: 31746766 (View on PubMed)

Provided Documents

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Document Type: Study Protocol and Statistical Analysis Plan

View Document

Other Identifiers

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REC10186

Identifier Type: -

Identifier Source: org_study_id

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