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Internet-based Intervention to Promote a Healthy Lifestyle on the Reproductive Parameters of Overweight and Obese Women

Efficacy of an Internet-based Intervention to Promote a Healthy Lifestyle on the Reproductive Parameters of Overweight and Obese Women: a Randomised Controlled Trial

Status
Withdrawn
Phases
NA
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT04275869
Acronym
HLRP-RCT
Enrollment
0
Registered
2020-02-19
Start date
2020-02-27
Completion date
2024-04-30
Last updated
2025-02-12

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Infertility, Female, Obesity

Keywords

infertility, obesity, physical activity, nutrition, internet

Brief summary

Obesity and overweight are among the problems that produce infertility. The combination of diet and exercise to achieve weight loss are currently considered an effective intervention for the improvement of reproductive parameters in overweight or obese infertile women. Aim: to evaluate the effectiveness of an online program to promote a healthy lifestyle among women who are overweight or obese who also have a diagnosis of infertility and are on the waiting list for in vitro fertilisation treatment

Detailed description

Weight management problems (being obese or overweight) are among the problems that produce infertility. The combination of diet and exercise to achieve weight loss are currently considered an effective intervention for the improvement of reproductive parameters in overweight or obese infertile women. Aim: to evaluate the effectiveness of a 3-month internet-based program focusing on the promotion of healthy lifestyles (especially weight loss and healthy eating and physical exercise habits) in women who also have a diagnosis of infertility and are on the waiting list for IVF treatment. Design: randomised controlled trial Setting: Hospital La Plana (Villarreal)

Interventions

OTHERHealthy Lifestyle

A 3-month internet-based program focusing on the promotion of healthy lifestyles. The treatment protocol comprises 9 modules which incorporate psychological strategies to promote healthy lifestyles by gradually changing eating and physical activity habits.

Sponsors

Hospital Universitario de la Plana
CollaboratorOTHER
Cardenal Herrera University
Lead SponsorOTHER

Study design

Allocation
RANDOMIZED
Intervention model
PARALLEL
Primary purpose
TREATMENT
Masking
DOUBLE (Investigator, Outcomes Assessor)

Eligibility

Sex/Gender
FEMALE
Age
18 Years to 40 Years
Healthy volunteers
No

Inclusion criteria

* women of childbearing age * overweight (BMI \> 25 kg/m2) or obese (BMI \> 30 kg/m2) * diagnosed with primary infertility -access to the internet-

Exclusion criteria

* over 40 years * morbid or extreme obesity (BMI \> 40 kg/m2) * bilateral obstruction of the fallopian tubes * endometriosis * women whose partner has a severe male factor (oligoasthenoteratozoospermia).

Design outcomes

Primary

MeasureTime frameDescription
Spontaneous clinical pregnancy rate12 monthsThe primary outcome will be the spontaneous clinical pregnancy rate (pregnancy with ultrasound visualisation of the gestational sac at week 7 of pregnancy) and evolution (pregnancy with ultrasound visualisation of the gestational sac and a heartbeat after 20 weeks of gestation).

Secondary

MeasureTime frameDescription
Body mass index (BMI)12 monthsWeight (in kilograms) and height (in meters) will be combined to report BMI in kg/m\^2.
Abdominal perimeter12 monthsIt will be measured with a tape-measure at the level of the navel (without compressing the skin tissue) and after drawing in air following one deep inhalation and exhalation.
Mediterranean Diet Adherence12 monthsMediterranean Diet Adherence Screener (MEDAS) questionnaire used in the PREDIMED trial. This questionnaire has been validated for the Spanish population and assesses adherence to the Mediterranean diet.
Physical activity level12 monthsThis is a self-administered questionnaire comprising 7 items which collects information about the physical activity the surveyee has completed in 7 days prior to completing the test. The IPAQ-SF will be used to calculate the total number of minutes and days the person has engaged in physical activity by adding all physical activity category scores from the prior 7 days together. This data will be converted into metabolic equivalent of task minutes per week (MET-min/week), using the formula published by Ainsworth et al., to classify their physical activity levels as 'high' (\> 1,500 MET-min/week), 'moderate' (600-1,500 MET-min/week), or 'low' (\< 600 MET-min/week).

Countries

Spain

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 4, 2026