Pregnancy Related Clinical Trial
Official title:
The Effect of Mindfulness-Based Web-Based Stress Reduction Program Applied to Primigravidas on Perceived Stress Level in Pregnancy, Birth Self-Efficacy and Prenatal Attachment
Verified date | March 2024 |
Source | Ataturk University |
Contact | n/a |
Is FDA regulated | No |
Health authority | |
Study type | Interventional |
The aim of this study is to investigate the effect of a mindfulness-based web-based stress reduction program applied to primigravidas on perceived stress level in pregnancy, birth self-efficacy and prenatal attachment.
Status | Not yet recruiting |
Enrollment | 90 |
Est. completion date | May 1, 2025 |
Est. primary completion date | December 1, 2024 |
Accepts healthy volunteers | Accepts Healthy Volunteers |
Gender | Female |
Age group | 18 Years to 35 Years |
Eligibility | Inclusion Criteria: - Graduated from at least primary school - Having a computer or a cell phone, - Having access to the Internet, - Being between the ages of 18-35, - Being 18-24 weeks pregnant, - Having a single healthy fetus, - Being primigravida, - Not having a risky pregnancy (such as placenta previa, preeclampsia, not having any systemic disease), - Not participating in any childbirth preparation class - Not having a neurological or psychiatric disease. Exclusion Criteria: - Voluntary withdrawal from the study - Failure to complete the 8-module training for any reason - Interruption of internet access and inability to communicate - Termination of pregnancy for any reason - Non-participation in the trainings given in the experimental group |
Country | Name | City | State |
---|---|---|---|
n/a |
Lead Sponsor | Collaborator |
---|---|
Ataturk University |
Type | Measure | Description | Time frame | Safety issue |
---|---|---|---|---|
Primary | Pregnancy Stress Assessment Scale (PSAS) | The initial scale consisting of 40 items was revised as 36 items as a result of the validity and reliability study conducted in Taiwan. The scale consists of seven (7) sub-dimensions and is 5-point Likert type. Each item is evaluated as (absolutely no (0), mild (1), moderate (2), severe (3), very severe (4)). The lowest score that can be obtained from the scale is 0 and the highest score is 144. | Two months | |
Primary | Self-Efficacy Scale for Normal Childbirth | There are 9 items in the scale. For each item in the scale, scores from 0 to 10 are given and scored as 0 points = no confidence at all and 10 points = very confident. The lowest score that can be obtained from the Self-Efficacy Scale for Normal Birth is 0, while the highest score that can be obtained is 90. As the scores obtained from the self-efficacy scale increase, the degree of self-efficacy also increases. | Two months | |
Primary | Prenatal Attachment Inventory (PAI) | The inventory consists of 21 items and is four-point Likert type. The items of the inventory are scored between 1 and 4 points as 1-Never, 2-Sometimes, 3-Frequently, 4-Always. A minimum of 21 and a maximum of 84 points can be obtained from the inventory. An increase in the score obtained from the inventory indicates an increase in the level of attachment. | Two months |
Status | Clinical Trial | Phase | |
---|---|---|---|
Completed |
NCT05017974 -
Research on Improving Sleep During Pregnancy
|
N/A | |
Completed |
NCT03284515 -
Vaccination In Pregnancy Gene Signature: VIP Signature Study
|
||
Recruiting |
NCT05969795 -
Comparison of Live Birth Rate in Natural Cycle Single Euploid FET Versus Without Luteal Phase Support
|
Phase 1 | |
Recruiting |
NCT06051201 -
Innovation for Small-scale Experiments: ReceptIVFity Test
|
N/A | |
Recruiting |
NCT04828382 -
Prospective Study of Pregnancy in Women With Cystic Fibrosis
|
||
Enrolling by invitation |
NCT04527926 -
STEPuP: Prenatal Provider Education and Training to Improve Medication-assisted Treatment Use During Pregnancy
|
N/A | |
Recruiting |
NCT04278651 -
Early Antenatal Support for Iron Deficiency Anemia
|
Phase 4 | |
Recruiting |
NCT04405700 -
Measuring Adverse Pregnancy and Newborn Congenital Outcomes
|
||
Recruiting |
NCT06258902 -
Odevixibat Pregnancy and Lactation Surveillance Program: A Study to Evaluate the Safety of Odevixibat During Pregnancy and/or Lactation
|
||
Completed |
NCT05487196 -
Effectiveness of Clonidine, Dexmedetomidine, and Fentanyl Adjuncts for Labor Epidural Analgesia
|
Phase 2 | |
Completed |
NCT03750968 -
Lutein & Zeaxanthin in Pregnancy - Carotenoid Supplementation During Pregnancy: Ocular and Systemic Effects
|
Phase 2 | |
Enrolling by invitation |
NCT06127277 -
Next4You: A Fully Mobile Relationships Based Program for Youth in Foster Care
|
N/A | |
Completed |
NCT05897697 -
Assessing Women's Preferences for Postpartum Thromboprophylaxis: the Prefer-Postpartum Study
|
||
Recruiting |
NCT05899101 -
The Impact of Opioid and Cannabis Exposure on Fetal Growth
|
||
Completed |
NCT05502510 -
Assessing the Effectiveness and Efficacy of the MyHealthyPregnancy Application
|
||
Completed |
NCT04296396 -
Opioid Prescription After Cesarean Trial
|
Phase 3 | |
Not yet recruiting |
NCT06069856 -
Multiple Micronutrient Supplementation (MMS) IFA- Iron Dose Acceptability Crossover Trial
|
Phase 3 | |
Not yet recruiting |
NCT06069869 -
Multiple Micronutrient Supplementation (MMS) Iron Dose Acceptability Crossover Trial
|
Phase 3 | |
Not yet recruiting |
NCT06163651 -
Evaluating a One-Year Version of the Parent-Child Assistance Program
|
N/A | |
Not yet recruiting |
NCT06079918 -
Multiple Micronutrient Supplementation for Maternal Anemia Prevention in Tanzania
|
Phase 3 |