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Completed

NCT Number: NCT02405611

A Multi-component Intervention on Improving Fruit and Vegetable Consumption in Teenagers and Their Mothers

This study is a longitudinal controlled trial that is designed to investigate the effectiveness of a multi-component intervention on improving fruit and vegetable consumption in teenagers and their mothers.

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Key information

Conditions

Sex eligibility

All sexes

Study type

Interventional

Phase

Not applicable

Primary location

Department of Public Health, Qazvin University of Medical Sciences, Qazvin, Qazvin Province, Iran

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About this study

This study is a longitudinal controlled trial that is designed to investigate the effectiveness of a multi-component intervention on improving fruit and vegetable consumption in teenagers and their mothers. Participants will be allocated in three groups with a) an intervention group in which mothers and children receive the intervention and questionnaires, b) only the children receive the intervention and mothers and children receive the questionnaires, and c) mothers and children are in active control group and only receive the questionnaires. The intervention package contains behavior change techniques targeting outcome expectancy, self-efficacy, action planning, coping planning, and self-monitoring. The active control group receives an information sheet regarding recommendations on fruit and vegetable intake. There will be 3 assessment points in time, with 1 months in between. All the intervention materials and information sheets will be handed to participants after the baseline assessment. The self-monitoring calendar will be collected at time 2 assessment.

The primary outcome of this study is to estimate the dyadic mechanisms between mothers and their children regarding improving fruit and vegetable intake. Secondary outcome is to investigate whether fruit and vegetable consumption did improve in the intervention groups in general and also to find the psychological mechanism behind the changes during the time of the study.

Who can participate

Healthy volunteers accepted: Yes

Only the study team can determine whether someone qualifies for participation.

Inclusion criteria

  • They are not involved in the nutritional education
  • Ability to understand Persian language Adolescents attending high schools in Qazvin

Exclusion criteria

  • Does not meet inclusion criteria

Treatment and study plan

Behavioral

Behavioral

The intervention package contains behavior change techniques targeting outcome expectancy, self-efficacy, action planning, coping planning, and self-monitoring. The active control group receives an information sheet regarding recommendations on fruit and vegetable intake. There will be 3 assessment points in time, with 1 month and six months in between. All the intervention materials and information sheets will be handed to participants after the baseline assessment. The self-monitoring calendar will be collected at time 2 assessment.

primary eduction

Behavioral

The intervention package contains behavior change techniques targeting outcome expectancy, self-efficacy, action planning, coping planning, and self-monitoring. The active control group receives an information sheet regarding recommendations on fruit and vegetable intake. There will be 3 assessment points in time, with 1 1 month and six months in between. All the intervention materials and information sheets will be handed to participants after the baseline assessment. The self-monitoring calendar will be collected at time 2 assessment.

Primary outcomes

  1. changes in fruit intake using a self-reported questionnaire

    Time frame: baseline, 1 Months, 6 months follow-up

    using a self-reported questionnaire

  2. changes in vegetable intake using a self-reported questionnaire

    Time frame: baseline, 1 Months, 6 months follow-up

    using a self-reported questionnaire

Secondary outcomes

  1. changes in self efficacy using a self-reported questionnaire

    Time frame: baseline, 1 Months, 6 months follow-up

    using a self-reported questionnaire

  2. changes in outcome expectancy using a self-reported questionnaire

    Time frame: baseline, 1 Months, 6 months follow-up

    using a self-reported questionnaire

  3. changes in coping planning using a self-reported questionnaire

    Time frame: baseline, 1 Months, 6 months follow-up

    using a self-reported questionnaire

  4. changes in action planning using a self-reported questionnaire

    Time frame: baseline, 1 Months, 6 months follow-up

    using a self-reported questionnaire

  5. changes in self-monitoring using a self-reported questionnaire

    Time frame: baseline, 1 Months, 6 months follow-up

    using a self-reported questionnaire

Sponsors and collaborators

Lead sponsor

Qazvin University Of Medical Sciences

Other

Registry information

Important dates

Study start
2015
Primary completion
2015
Study completion
2016
First posted
Apr 1, 2015
Registry last updated
Jul 25, 2016

OpenTrials presents study information sourced from ClinicalTrials.gov. The official registry record should be consulted for the latest information.

View the official ClinicalTrials.gov record (opens in a new tab)

This listing is for discovery and informational purposes only. It is not medical advice, does not guarantee that a study is recruiting, and does not determine eligibility. Contact the study team and a qualified healthcare professional when considering participation.

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