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Pregnancy Related clinical trials

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NCT ID: NCT04167423 Completed - Quality of Life Clinical Trials

Mapping Health-related Quality of Life in Pregnant Women With Thyroid Disease.

ThyPreQol2020
Start date: January 14, 2020
Phase:
Study type: Observational

Natural thyroid function changes during pregnancy. In up to tens of percent of pregnant women, these changes can lead to pathological fluctuations in hormone and antibody production. Although the effects on pregnancy and child development are well described, none has determined their influence on mother's emotional well-being and the quality of life. At present, universal thyroid screening in pregnancy in the Czech Republic is not covered by health insurance. The aim of the project is to change this situation by providing quality of life estimate for the cost-effectiveness model. This is a project of three specialized institutions aimed at mapping various aspects of the quality of life of pregnant women and describing the impact of thyroid disease on their lives. The project is a parallel study to a larger project Early screening for thyreopathy in pregnancy (CZ.03.2.63/0.0/0.0/15_039/0009643) supported by the European Fund Operational Programme Employment through the National screening centre. The data will be collected through online questionnaire from women enrolled in the Early screening for thyreopathy in pregnancy (CZ.03.2.63/0.0/0.0/15_039/0009643) who were screened for TSH, TPOAb and FT4.

NCT ID: NCT04158401 Completed - Pregnancy Related Clinical Trials

Cervical Stiffness Measurement in Cervical Insufficiency

Start date: January 15, 2020
Phase:
Study type: Observational

The goal of this cross sectional study is to evaluate the differences in cervical stiffness between patients who present for cerclage placement versus normal pregnancies. The central hypothesis is that women for whom a cerclage is indicated will have cervical stiffness measurements lower than normal controls. Cervical stiffness will be objectively measured by the closing pressure Pcl using the Pregnolia measurement device. This is performed during a speculum exam by placing the measurement probe on the ectocervix. In current clinical care, there is no objective measurement of cervical stiffness. An accurate measurement of cervical stiffness that correlates with clinical outcome will advance the field. Successful completion of the current study will spark future studies that correlate cervical stiffness pcl in a prospective study.

NCT ID: NCT04157309 Completed - Pregnancy Related Clinical Trials

Alternating Urine Redox Status Of Consecutive Menstrual Cycles

ACDC
Start date: January 6, 2020
Phase:
Study type: Observational

This study will involve the collection and analysis of urine samples from non-pregnant women to determine the existence of alternating redox status between two consecutive menstrual cycles.

NCT ID: NCT04146025 Completed - Pregnancy Related Clinical Trials

Nurtured in Nature

Start date: September 12, 2019
Phase: N/A
Study type: Interventional

The investigators pilot test a Nature Coach Intervention in a population of postpartum women, to increase the amount of time people spend outside in local nature, with the goal of preventing postpartum depression.

NCT ID: NCT04098016 Completed - Pregnancy Related Clinical Trials

Digital Intervention To Improve Diet Quality

Start date: March 8, 2021
Phase: N/A
Study type: Interventional

This study will develop a digital intervention ("Healthy Roots") adapted from a previously tested adult digital obesity treatment intervention ("Track").

NCT ID: NCT04079608 Completed - Pregnancy Related Clinical Trials

Rigorous Evaluation of High School FLASH

Start date: October 5, 2016
Phase: N/A
Study type: Interventional

High School FLASH is a 15-session comprehensive sexual health curriculum designed for classroom settings in grades 9 to 12. The basis of High School FLASH is a public health approach to behavior change. The primary strategy used in the FLASH curriculum for preventing teen pregnancy, sexually transmitted diseases (STDs), and sexual violence is to address student behaviors and attitudes. To this end, FLASH uses a harm reduction and behavior change framework, implements best practices as outlined in the research on effective programs, addresses risk and protective factors for program goals, and rests on the theory of planned behavior. The instructional approach of High School FLASH employs key concepts in every lesson, which enables teachers to hone in on the risk and protective factors outlined in the curriculum logic model. The curriculum covers the following topics: reproductive system, pregnancy, sexual orientation and gender identity, healthy relationships, coercion and consent, online safety, abstinence, birth control, preventing human immunodeficiency virus (HIV) and other STDs, condoms, STD testing, communicating and decision making, and improving school health. The curriculum aligns with national health education standards.

NCT ID: NCT04064320 Completed - Anxiety Clinical Trials

The Effect of Lullaby Intervention on Anxiety and Attachment in Pregnancy

Start date: June 6, 2017
Phase: N/A
Study type: Interventional

The aim of present study was to investigate the effect of lullaby intervention on anxiety and prenatal attachment in women with high-risk pregnancy. The study involved women with high-risk pregnancy who were assigned randomly to the intervention (n=30) or control (n=30) groups in a state hospital in Turkey. For two successive days, the intervention group listened to lullabies for 20 minutes once a day, meanwhile touched the abdomen and thought about their babies, but the control group did not. Data from the outcomes of anxiety and attachment were collected at baseline and at the end of the second day. Vital findings were measured on each study day, both before and after the lullaby intervention/usual care.

NCT ID: NCT04058873 Completed - Pregnancy Related Clinical Trials

A Study on the Feasibility and Acceptability of Pericoital Levonorgestrel 1.5mg

Start date: October 1, 2019
Phase:
Study type: Observational

This study intends to build on the previous research and gather data in an actual use study / patient registry of pericoital LNG 1.5mg to understand women's acceptability of the product along with associated side effects, and monitoring for their correct and incorrect use. These findings will contribute to the discussion around the feasibility of pericoital LNG as an additional contraceptive by adding to the body of evidence.

NCT ID: NCT04020432 Completed - Pregnancy Related Clinical Trials

Knowledge Assessment of Women About Pictograms Associated With the Danger of Medicines Taken During Pregnancy

ECOFP
Start date: July 11, 2019
Phase:
Study type: Observational

Women's awareness about the danger of certain medicines taken during pregnancy presents a real public health issue. To enhance awareness and information for women and healthcare professionals, new pictograms " pregnant women " appeared on medication boxes, on October 16, 2017. These new pictograms can change women's perception of self-medication during pregnancy and of the danger of taking certain medicines for the unborn development. Furthermore, the investigators can wonder if the meaning of these pictograms is well understood. Therefore, the study's primary aim is to assess the knowledge of pregnant or childbearing age women about the pictograms associated with the danger of certain medicines taken during pregnancy.

NCT ID: NCT04018625 Completed - Anxiety Clinical Trials

The Stony Brook University Calm-Mom Study

Start date: April 1, 2021
Phase: N/A
Study type: Interventional

The present trial will evaluate the feasibility, acceptability and preliminary efficacy of 2 different internet-delivered programs for prenatal maternal stress. The Stress Managment and Resiliency Training Program (SMART-Mom program), an 8-session Cognitive Behavior Therapy (CBT) based mind body program and the Mama Support Program, an 8-session social support group program. Sixty pregnant women (<20 weeks Estimated Gestational Age) will be screened and either enrolled in the online SMART Mom Program or the Mama Support Program. Outcomes, including maternal perceived stress, depression, and anxiety will be assessed at post-treatment, three, and six months post program completion. Potential impact on infant health outcomes will be assessed via post-delivery electronic medical record review.