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Completed

NCT Number: NCT03688087

Study of Programm Interest 'Bouge' to Improve the Daily Physical Activity at the Pregnant Women.

Evaluate the "Bouge" digital program (smartphone application) to increase the daily physical activity of pregnant patients beguining at 15 SA

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Key information

Conditions

Physical Activity Behavior Mobile Health Apps Motor Activity Pregnant

Age range

18 year and older

Sex eligibility

Female

Study type

Interventional

Phase

Not applicable

Primary location

CHRU de Brest, Brest, France

Loading trial locations.

About this study

Controlled, randomized, open, prospective, multicentric study, 250 pregnant patients aged between 18 and more, with 14 weeks of amenorrhea, possessing a smartphone, will be recruited and randomized into two groups:

125 in the control group (smartphone application "placebo" = number of steps) 125 will be equipped with the application "Bouge" = coached group

For three months, the patients do their daily physical activity. The "coached" group, through the smartphone application "Bouge", receives computer coaching to increase their physical activity (no direct medical intervention, only notifications and computer pusch).

The control group is not coached by the application (simple display of the number of step)

Who can participate

Healthy volunteers accepted: No

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

Inclusion criteria

Pregnant <14 weeks of amenorrhea Must have a compatible smartphone

Exclusion criteria

Multiple pregnancies Pre-existing pregnancy-related diseases Pregnancy complicated History of peripheral arterial disease History of IUGR History of cone biopsy History of delivery hemorrhage

Treatment and study plan

Smartphone application "placebo"

Device

Strategy based on smartphone application "placebo"

Smartphone equipped with application "bouge" = Coach group

Device

Strategy based on smartphone application "bouge"

Primary outcomes

  1. Increased daily physical activity (number of steps) using the smartphone application "BOUGE"

    Time frame: 12 Weeks

    The objective is an increase of 2000 steps daily between J 1 and J 90 (an increase of 10 000 steps between S1 and S 12)

Secondary outcomes

  1. sleep,

    Time frame: 12 Weeks

    Scale Spiegel

  2. Well being

    Time frame: 12 Weeks

    Scale OMS

  3. - lumbago

    Time frame: 12 Weeks

    Scale EIFEL

Sponsors and collaborators

Lead sponsor

University Hospital, Brest

Other

Registry information

Official study title

Study of Program Interest "Bouge" to Improve the Daily Physical Activity and Tolerance in Processings Treatment of Pregnant Women

Acronym: BOUGE GROSSESS

Important dates

Study start
2017
Primary completion
2019
Study completion
2019
First posted
Sep 28, 2018
Registry last updated
Jun 8, 2026

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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