Infertility, Female, Lifestyle, Polycystic Ovarian Syndrome
Conditions
Brief summary
Patients will be randomly assigned to a group where they undergo a 12-week lifestyle modification program prior to their fertility treatment, or a group where they are entitled to start their fertility treatment without prior lifestyle modification program.
Detailed description
When allocated to the control arm patients will receive the standard of care combined with the foreseen questionnaires and bio-electric impedance analysis for body composition and ergospirometry. When the patient is allocated to the interventional arm she will receive a 12-week lifestyle modification program prior to her fertility treatment. The lifestyle modification program will consist of dietary advice, advice for physical activity and emotional support. After the 12-week program the fertilty treatment will start as per routine practice. Questionnaires, ergospirometry and bio-electric impedance analysis will also be performed at the foreseen moments.
Interventions
BEHAVIORALLifestyle program
If the patient is allocated to the interventional group, the lifestyle modification program will be planned/started immediately after the intake at the fertility clinic. The lifestyle modification program has a duration of 12 weeks in which the subject will receive follow-up by the endocrinologist/diabetologist and dietitian to re-ceive an active dietary intervention plan, follow-up by the physiotherapist where sessions to start with physical exercise will be given. Monthly follow-up visits with the coordinating PCOS-midwife will be planned to enhance the subject's knowledge about PCOS and give emotional support. At the moment of randomization, the PCOS coordinating midwife will immediately plan all necessary appointments, with the endocrinologist and dietitian, physiotherapist and PCOS-coordinator, for the 12-week lifestyle program. This way, patients will have a clear overview of the following 12 weeks.
Sponsors
Universitair Ziekenhuis Brussel
Study design
Allocation
RANDOMIZED
Intervention model
PARALLEL
Primary purpose
TREATMENT
Masking
NONE
Eligibility
Sex/Gender
FEMALE
Age
18 Years to 38 Years
Healthy volunteers
No
Inclusion criteria
* Subfertile patients between \>18- \<38 years old requesting fertility treatment at our centre * PCOS phenotypes A, B, C and D according to the NIH 2012 extension of the ESHRE/ASRM 2003 diagnostic criteria * BMI \>27 and \<38 (Jiskoot et al. 2017) * Nulliparous women * Patient gives consent voluntarily
Exclusion criteria
Patients will be excluded if they: * do not meet the ESHRE/ASRM 2003 diagnostic PCOS criteria * Have a BMI \<27 and \>38 (Jiskoot et al. 2017) * Need Surgical sperm retrieval * Use donor eggs * Need Pre-implantation genetic testing (PGT) * Multiparous women * cannot reliably fill out the questionnaires or comprehend the intervention, because of a language barrier
Design outcomes
Primary
| Measure | Time frame | Description |
|---|---|---|
| body weight | 12 weeks after start of intervention | body weight (kg) |
| body composition | 12 weeks after start of intervention | body composition (Total Body Fat and Fat Free Mass), measured by using bio-electric im-pedance analysis (BIA) |
Countries
Belgium
Outcome results
None listed