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临床试验/NL-OMON44770
NL-OMON44770招募中不适用

DIY health monitoring and simulation of health in pregnant women: a pilot study - oPTiMuM (PreganT Moms Measure)

TNO0 个研究点目标入组 40 人开始时间: 待定最近更新:
适应症

试验速览

阶段
不适用
状态
招募中
发起方
入组人数
40

研究概览

简要总结

暂无简介。

研究设计

研究类型
Observational

入排标准

年龄范围
18 至 99(—)

入选标准

  • 1. Pregnant between 12-18 weeks at the start of the study;
  • 2. Women must be able to speak, write and read in Dutch;
  • 3. Healthy as assessed by the Health and Lifestyle questionnaire (P9624 F02);
  • 4. Body mass index:
  • - BMI 18,5 - 25 for the lean group
  • - BMI * 30 for the obese group;
  • 5. Able to use self-monitoring devices;
  • 6. Voluntary participation;
  • 7. Having given written informed consent;
  • 8. Willing to comply with study procedures;
  • 9. Willingness to share pseudonymised data on measured health parameters with external parties that provide the measuring devices (including MijnEetmeter, Moves and NRC) for reasons of synchronisation with the study database;
  • 10. Willing to accept use of all nameless data, including publication, and the confidential use and storage of all data by TNO;
  • 11. Have internet access at home;
  • 12. Subjects should own a Smartphone that runs either a recent version of iOS or Android.

排除标准

  • 1. Use of concomitant medication;
  • 2. Having a history of medical or surgical events that may significantly affect the study outcome, including physical limitations or cardio-vascular events;
  • 3. Having a (history of a) medical condition that might significantly affect the study outcome as judged by the principal investigator and health and life style questionnaire. This includes diabetes type 1 or 2, gastrointestinal dysfunction, diseases related to inflammation, or a psychiatric disorder;
  • 4. Hypertension: systolic blood pressure >160 mmHg, diastolic blood pressure >90 mmHg;
  • 5. Having a pacemaker;
  • 6. Previous pregnancy with medical issues (e.g. pre-eclampsia);
  • 7. Reported slimming or medically prescribed diet;
  • 8. Physical, mental or practical limitations in using computerized systems;
  • 9. Alcohol consumption > 14 units (drinks)/week;
  • 10. Smoking;
  • 11. Reported unexplained weight loss or gain of > 2 kg in the three months prior to the pre-study screening / pregnancy;
  • 12. Recent blood donation (<1 month prior to the start of the study);
  • 13. Not willing to give up blood donation during the study;
  • 14. Personnel of TNO and their partner.

研究者

发起方
TNO

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