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Clinical Trial Details — Status: Not yet recruiting

Administrative data

NCT number NCT05331586
Other study ID # 0000
Secondary ID
Status Not yet recruiting
Phase N/A
First received
Last updated
Start date July 2022
Est. completion date May 2023

Study information

Verified date February 2022
Source Universidade do Porto
Contact n/a
Is FDA regulated No
Health authority
Study type Interventional

Clinical Trial Summary

Pregnant women with obesity will be invited to participate in structured home-based exercise programme, remotely monitored


Description:

Pregnant women with obesity will be invited to participate in structured home-based exercise programme, remotely monitored. The remote system use inertial motion trackers, digitizes pregnant women motion and provides real-time feedback on performance through a mobile app. It also includes a web-based platform that allows the clinical team to prescribe, monitor and adapt the exercise program remotely. This way, the system allows patients to perform independent exercise program at home without the need for constant therapist supervision, ensuring remote monitoring throughout the rehabilitation program. The exercise programme will be performed since the first gestational trimester until delivery. Data of gestational weight gain, gestational diabetes mellitus, low back pain and quality of life will be colected.


Recruitment information / eligibility

Status Not yet recruiting
Enrollment 40
Est. completion date May 2023
Est. primary completion date December 2022
Accepts healthy volunteers Accepts Healthy Volunteers
Gender Female
Age group 18 Years and older
Eligibility Inclusion Criteria: - Pregnant women with obesity (BMI = 30 kg/m2) at first gestational trimester Exclusion Criteria: - pre-pregnancy BMI < 30 kg/m2; - previous bariatric surgery; - hemodynamically significant heart disease; - restrictive lung disease; - incompetent cervix or cerclage; - multiple gestation; - persistent second- or third-trimester bleeding; - placenta previa after 26 weeks of gestation; - premature labor during the current pregnancy; - ruptured membranes; - preeclampsia or pregnancy-induced hypertension; - severe anemia; - inability to read and understand Portuguese; ->15 weeks gestation.

Study Design


Related Conditions & MeSH terms


Intervention

Behavioral:
Remote Exercise
The pregnant women will perform a home-based structured exercise programme. The exercise will be remotely monitored since the first gestational trimester until delivery

Locations

Country Name City State
Portugal Diana Bernardo Porto

Sponsors (2)

Lead Sponsor Collaborator
Universidade do Porto Fundação para a Ciência e a Tecnologia

Country where clinical trial is conducted

Portugal, 

Outcome

Type Measure Description Time frame Safety issue
Primary Gestational Weight Gain Using portable digital scale (Tantita InnerScan BC-545). Gestational weight gain will be calculated as the difference between maternal weight at last appointment (36-39 gestational weeks) and pre-pregnancy weight. At delivery
Primary Excessive gestational weight gain The adequate gestational weight gain in pregnant women with obesity should not exceed 9kg in entire pregnancy, the values over these thresholds will be considered excessive gestational weight gain. At delivery
Secondary Low Back Pain Oswestry Low Back Pain Disability Questionnaire (ODI v2.0) At first, second and third gestational trimester
Secondary Subjective Physical Activity assessment Pregnancy Physical Activity Questionnaire (PPAQ) is a self-reported questionnaire. The objective is measure the type and intensity of pregnant women physical activity. At first, second and third gestational trimester
Secondary Objective Physical Activity assessment Accelerometry, is a device that monitors the acceleration of body segments, it is considered the gold standard with regard to objectivity and reliability (ICC:0.661-0.806) At first, second and third gestational trimester
Secondary Gestational Diabetes Mellitus The presence of gestational diabetes mellitus will be assessed between 24-28 gestation weeks, through the Oral Glucose Tolerance Test. Blood sampling for fasting glucose concentrations will be taken after a 10 hour overnight fast, and glucose tolerance will measured by a 2 hours 75 mg per-oral glucose tolerance test. GDM will be diagnosed as fasting glucose = 126 mg/dl or 2h concentration = 200 mg/dl. Second gestational trimester
Secondary Quality of Life Assessment COOP-Quality of life during Pregnancy Questionnaire At first, second and third gestational trimester
Secondary Pelvic Floor and sexual disorders during pregnancy Assessment of Pelvic Floor Disorders and Their Risk Factors During Pregnancy and Postpartum Questionnaire At first, second and third gestational trimester
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