HMOVE: Aerobe Cycling Training in Women With Unexplained Recurrent Pregnancy Loss

Sponsor
Radboud University Medical Center (Other)
Overall Status
Recruiting
CT.gov ID
NCT06007560
Collaborator
Maastricht University Medical Center (Other)
30
2
1
28.4
15
0.5

Study Details

Study Description

Brief Summary

In 50% of women with recurrent pregnancy loss (RPL) miscarriages are unexplained, therefore no therapeutic intervention is possible. In a pilot study, women with unexplained RPL showed less endometrial NK cells (eNK) compared to women with a previously uncomplicated pregnancy. It is known that eNK cells are important for embryo implantation during early pregnancy. Investigators presume that high sympathetic activity in these women is related to eNK cell number, function and phenotype and that exercise is an effective intervention to lower sympathetic activity and to influence the immune system, as especially peripheral NK cells have been assumed to be responsive to physical training. The investigators hypothesize that moderate exercise can lower the adrenergic tone of the sympathetic nervous system hereby influencing endometrial NK cells in women with RPL and eventually pregnancy outcome.

Condition or Disease Intervention/Treatment Phase
  • Other: Exercise
N/A

Study Design

Study Type:
Interventional
Anticipated Enrollment :
30 participants
Allocation:
N/A
Intervention Model:
Single Group Assignment
Masking:
None (Open Label)
Primary Purpose:
Basic Science
Official Title:
Aerobe Cycling Training in Women With Unexplained Recurrent Pregnancy Loss
Actual Study Start Date :
Mar 21, 2022
Anticipated Primary Completion Date :
Aug 1, 2024
Anticipated Study Completion Date :
Aug 1, 2024

Arms and Interventions

Arm Intervention/Treatment
Other: <80% eNK

Women with low eNK bright cell numbers, defined as <80% of the total endometrial NK cell population

Other: Exercise
Aerobe cycling training consisting of 12-weeks of HR-controlled training at 50-60% of VO2max (maximal oxygen uptake) for 1 hour, for 2 times (week: 1-6) to 3 times (week: 7-12) per week

Outcome Measures

Primary Outcome Measures

  1. CD56 endometrial NK cell frequency [3 months]

    Change in CD56 eNK cell frequency measured as percentage of total lymphocyte or total CD56 population by flowcytometry.

  2. CD56 endometrial NK cell function [3 months]

    Change in CD56 eNK cell function measured as percentage of CD56 degranulation by flowcytometry.

Secondary Outcome Measures

  1. CD56 endometrial NK cell phenotype [3 months]

    Change in CD56 eNK cell phenotype measured as percentage of (sub)population or mean fluorescent intensity respectively by flowcytometry.

  2. CD56 peripheral NK cell frequency [3 months]

    Change in CD56 pNK cell frequency measured as percentage of total lymphocyte or CD56 population by flowcytometry.

  3. CD56 peripheral NK cell function [3 months]

    Change in CD56 pNK cell function measured as percentage of CD56 degranulation by flowcytometry.

  4. CD56 peripheral NK cell phenotype [3 months]

    Change in CD56 pNK cell phenotype measured as percentage of (sub)population or mean fluorescent intensity respectively by flowcytometry.

  5. Vaginal microbiome [3 months]

    Change in taxonomic classification of vaginal microbiota of different subtypes but also classified in clustering of different subtypes.

  6. Metabolic syndrome parameters I [3 months]

    Change in cm waist circumference.

  7. Metabolic syndrome parameters II [3 months]

    Chance in mmHg blood pressure, both systolic as diastolic.

  8. Metabolic syndrome parameters III [3 months]

    Change in concentration (mg/dL) triglyceride.

  9. Metabolic syndrome parameters IV [3 months]

    Change in concentration (mg/dL) cholesterol levels.

  10. Metabolic syndrome parameters V [3 months]

    Change in concentration (mg/dL) blood sugar levels.

  11. Sympathetic activity [3 months]

    Change in baroreceptor sensitivity in ms/mmHg.

  12. Uterine blood flow [3 months]

    Change in pulsatility index, lower indicates better outcome.

  13. Physical fitness [3 months]

    Change in VO2max.

  14. Pregnancy rate and live birth rate after one year of intervention, higher rater indicate better outcome. [3 months]

    Questionnaire.

Eligibility Criteria

Criteria

Ages Eligible for Study:
N/A to 40 Years
Sexes Eligible for Study:
Female
Accepts Healthy Volunteers:
No
Inclusion Criteria:
  • RPL defined as 2 or more unexplained pregnancy losses from the time of conception until 24 weeks of gestation, known cause for the miscarriages are the presence of thyroid abnormalities, anti-phospholipid syndrome, uterine malformation, and abnormal parental karyotype according to international guideline.

  • Couples should not be aiming to conceive during the time course of the exercise intervention.

Exclusion Criteria:
  • Age above 40 years

  • BMI above 40

  • Current use of immunosuppressive or biological drugs

  • Current use of hormone conceptive

  • HIV positivity

  • Current or recent (<2 weeks) symptomatic genital infection such as chlamydia, gonorroa, or pelvic inflammatory disease

  • Pre-existent diabetes mellitus, autoimmune disease or overt cardiovascular disease

  • Vaccination (i.e Covid) within 1 month prior to or during sampling and intervention

  • New pregnancy at time of measurements, breastfeeding

  • Current or recent (<2-3 months ago) pregnancy

  • (Physical) inabilities to follow moderate aerobe cycling training

  • Participants who are not capable of signing the informed consent

Contacts and Locations

Locations

Site City State Country Postal Code
1 Maastricht UMC+ Maastricht Netherlands 6202 AZ
2 Radboud UMC Nijmegen Netherlands 6500 HB

Sponsors and Collaborators

  • Radboud University Medical Center
  • Maastricht University Medical Center

Investigators

  • Principal Investigator: Tess Meuleman, Radboud University Medical Center

Study Documents (Full-Text)

None provided.

More Information

Publications

None provided.
Responsible Party:
Tess Meuleman, Principal Investigator, Radboud University Medical Center
ClinicalTrials.gov Identifier:
NCT06007560
Other Study ID Numbers:
  • HMOVE
First Posted:
Aug 23, 2023
Last Update Posted:
Aug 23, 2023
Last Verified:
Aug 1, 2023
Individual Participant Data (IPD) Sharing Statement:
No
Plan to Share IPD:
No
Studies a U.S. FDA-regulated Drug Product:
No
Studies a U.S. FDA-regulated Device Product:
No
Keywords provided by Tess Meuleman, Principal Investigator, Radboud University Medical Center
Additional relevant MeSH terms:

Study Results

No Results Posted as of Aug 23, 2023