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Virtual Reality, Labor Pain, Anxiety, Birth Perception

Primary Purpose

Labor Pain, Anxiety

Status
Completed
Phase
Not Applicable
Locations
Turkey
Study Type
Interventional
Intervention
Standard of care+virtual reality glasses
Sponsored by
Abant Izzet Baysal University
About
Eligibility
Locations
Arms
Outcomes
Full info

About this trial

This is an interventional supportive care trial for Labor Pain focused on measuring labor, pain, anxiety, birth perception, virtual reality

Eligibility Criteria

18 Years - 35 Years (Adult)FemaleAccepts Healthy Volunteers

Inclusion Criteria:

  • Able to communicate verbally
  • Between the ages of 18-35
  • No pregnancy-related risk diagnosis,
  • Primiparous,
  • Vaginal delivery planned,
  • Gestational week is between 37-42,
  • Single, live fetus and head presentation,
  • In the latent phase (1-3 cm) on admission to the delivery room,
  • Not having any dystocia that may affect the duration of labor (placental dystocia, pelvic dystocia, etc.).
  • No induction,
  • No epidural anaesthesia.
  • Pregnant women without vision and hearing problems were included in the study.

Exclusion Criteria:

  • Refusing to participate in the research,
  • Diagnosed with risky pregnancy,
  • Watching the video in active phase for less than 20 minutes
  • Watching the video in transition phase for less than 10 minutes
  • Cesarean section
  • Pregnant women who used any pharmacological analgesia were not included in the study.

Sites / Locations

  • İzzet Baysal State Hospital, Obstetrics and Pediatrics Unit, delivery room service

Arms of the Study

Arm 1

Arm 2

Arm Type

No Intervention

Experimental

Arm Label

Standard of care

Standard of care+ virtual reality glasses

Arm Description

Introductory information form (IIF), labor follow-up form (FFL) and VAS-P, VAS-A were filled in the latent phase (1-3 cm). At the beginning of the active (4 cm) and transitional phases (8 cm), FFL, VAS-P and VAS-A were filled and no intervention was applied. 20 min in active phase. then, FFL, VAS-P and VAS-A were filled after 10 min in the transition phase. The Perception of Birth Scale is filled after birth.

Introductory information form (IIF), labor follow-up form (FFL) and VAS-P, VAS-A were filled in the latent phase (1-3 cm). At the beginning of the active (4 cm) and transitional phases (8 cm), after filling FFL, VAS-P and VAS-A, video was watched with virtual reality glasses. 20 minutes in active phase after watching the video. then, FFL, VAS-P and VAS-A were filled after 10 min in the transition phase. After the birth, the Perception of Birth Scale and Virtual Reality Satisfaction Form were filled.

Outcomes

Primary Outcome Measures

pre-intervention pain at the start of the active phase was assessed by Visual Analogue Scale-Pain (VAS-P)
The scale is a 10 cm ruler that represents painlessness at one end (0=no pain) and the most severe pain (10=severe pain) at the other end. The patient is asked to put a line or mark on the point representing the intensity of pain. The part from the "no pain" point to the point marked by the participant is measured in mm and the value found indicates the patient's pain level.
post-intervention pain at the start of the active phase was assessed Visual Analogue Scale-Pain (VAS-P)
The scale is a 10 cm ruler that represents painlessness at one end (0=no pain) and the most severe pain (10=severe pain) at the other end. The patient is asked to put a line or mark on the point representing the intensity of pain. The part from the "no pain" point to the point marked by the participant is measured in mm and the value found indicates the patient's pain level.
pre-intervention anxiety at the start of the active phase was assessed by Visual Analogue Scale-Anxiety (VAS-A)
The scale is a 10 cm ruler representing the absence of anxiety (0 = no anxiety) at one end and the most severe anxiety (10 = severe anxiety) at the other end. The patient is asked to put a line or mark on the area showing the level of anxiety. The part from the no anxiety point to the point marked by the patient is measured in mm and the value found indicates the patient's anxiety level.
post-intervention anxiety at the start of the active phase was assessed by Visual Analogue Scale-Anxiety (VAS-A)
The scale is a 10 cm ruler representing the absence of anxiety (0 = no anxiety) at one end and the most severe anxiety (10 = severe anxiety) at the other end. The patient is asked to put a line or mark on the area showing the level of anxiety. The part from the no anxiety point to the point marked by the patient is measured in mm and the value found indicates the patient's anxiety level.
pre-intervention pain at the start of the transition phase was assessed by Visual Analogue Scale-Pain (VAS-P)
The scale is a 10 cm ruler that represents painlessness at one end (0=no pain) and the most severe pain (10=severe pain) at the other end. The patient is asked to put a line or mark on the point representing the intensity of pain. The part from the "no pain" point to the point marked by the participant is measured in mm and the value found indicates the patient's pain level.
post-intervention pain at the start of the transition phase was assessed by Visual Analogue Scale-Pain (VAS-P)
The scale is a 10 cm ruler that represents painlessness at one end (0=no pain) and the most severe pain (10=severe pain) at the other end. The patient is asked to put a line or mark on the point representing the intensity of pain. The part from the "no pain" point to the point marked by the participant is measured in mm and the value found indicates the patient's pain level.
pre-intervention anxiety at the start of the transition phase was assessed by Visual Analogue Scale-Anxiety (VAS-A)
The scale is a 10 cm ruler representing the absence of anxiety (0 = no anxiety) at one end and the most severe anxiety (10 = severe anxiety) at the other end. The patient is asked to put a line or mark on the area showing the level of anxiety. The part from the no anxiety point to the point marked by the patient is measured in mm and the value found indicates the patient's anxiety level.
post-intervention anxiety at the start of the transition phase was assessed by Visual Analogue Scale-Anxiety (VAS-A)
The scale is a 10 cm ruler representing the absence of anxiety (0 = no anxiety) at one end and the most severe anxiety (10 = severe anxiety) at the other end. The patient is asked to put a line or mark on the area showing the level of anxiety. The part from the no anxiety point to the point marked by the patient is measured in mm and the value found indicates the patient's anxiety level.
birth perception in the postpartum period was assessed by Mother's Perception of Birth Scale
The Mother's Perception of Birth Scale, which evaluates the experiences and perceptions of mothers at the time of birth, was developed by Fawcett and Knauth (144). The Turkish validity and reliability study of the scale was carried out by Güngör and Beji (2007). Experiences at the time of birth (7 items; 3, 5, 6, 8, 15, 17, 18), experiences during the pain period of labor (7 items; 1, 2, 4, 7, 9, 10, 16), postpartum (4 items) It consists of a total of 5 sub-dimensions and 25 items, namely; 22, 23, 24, 25), partner involvement (4 items; 11,12,20,21) and awareness (3 items; 13,14,19). Each item is scored from 1 to 5 in the Mother's Perception of Birth Scale. It is evaluated as 1-Not at all, 2-A little, 3-Moderate, 4-Very, 5-Very much. Since the questions 15-16-17-18-19 of the scale contain negative statements, scoring is done in reverse for these questions.

Secondary Outcome Measures

pre-intervention systolic blood pressure (mmHg) at the start of the active phase was assessed.
systolic blood pressure, measures the pressure in your arteries when your heart beats. Measurements were made with a blood pressure monitor.
post-intervention systolic blood pressure (mmHg) at the start of the active phase was assessed.
systolic blood pressure, measures the pressure in your arteries when your heart beats. Measurements were made with a blood pressure monitor.
pre-intervention diastolic blood pressure (mmHg) at the start of the active phase was assessed.
diastolic blood pressure, measures the pressure in your arteries when your heart rests between beats. Measurements were made with a blood pressure monitor.
post-intervention diastolic blood pressure (mmHg) at the start of the active phase was assessed.
diastolic blood pressure, measures the pressure in your arteries when your heart rests between beats. Measurements were made with a blood pressure monitor.
pre-intervention pulse (minute) at the start of the active phase was assessed.
The rhythmic dilation of an artery that results from beating of the heart. Measurements were made with a heart rate monitor.
post-intervention pulse (minute) at the start of the active phase was assessed.
The rhythmic dilation of an artery that results from beating of the heart. Measurements were made with a heart rate monitor.
pre-intervention respiration (minute) at the start of the active phase was assessed.
the inhaling of oxygen and the exhaling of carbon dioxide. is found by counting the number of breaths (how many times the chest rises).
post-intervention respiration (minute) at the start of the active phase was assessed.
the inhaling of oxygen and the exhaling of carbon dioxide. is found by counting the number of breaths (how many times the chest rises).
pre-intervention fetal heart rate (minute) at the start of the active phase was assessed.
Fetal heart rate was measured using a fetal Doppler device.
post-intervention fetal heart rate (minute) at the start of the active phase was assessed.
Fetal heart rate was measured using a fetal Doppler device.
pre-intervention contraction frequency (minute) at the start of the active phase was assessed.
Measurements were made using the NST device.
post-intervention contraction frequency (minute) at the start of the active phase was assessed.
Measurements were made using the NST device.
pre-intervention contraction duration (minute) at the start of the active phase was assessed.
Measurements were made using the NST device.
post-intervention contraction duration (minute) at the start of the active phase was assessed.
Measurements were made using the NST device.
pre-intervention contraction severity (minute) at the start of the active phase was assessed.
Measurements were made using the NST device.
post-intervention contraction severity (minute) at the start of the active phase was assessed.
Measurements were made using the NST device.
pre-intervention systolic blood pressure (mmHg) at the start of the transition phase was assessed.
systolic blood pressure, measures the pressure in your arteries when your heart beats. Measurements were made with a blood pressure monitor.
post-intervention systolic blood pressure (mmHg) at the start of the transition phase was assessed.
systolic blood pressure, measures the pressure in your arteries when your heart beats. Measurements were made with a blood pressure monitor.
pre-intervention diastolic blood pressure (mmHg) at the start of the transition phase was assessed.
diastolic blood pressure, measures the pressure in your arteries when your heart rests
post-intervention diastolic blood pressure (mmHg) at the start of the transition phase was assessed.
diastolic blood pressure, measures the pressure in your arteries when your heart rests
pre-intervention pulse (minute) at the start of the transition phase was assessed.
The rhythmic dilation of an artery that results from beating of the heart. Measurements were made with a heart rate monitor.
post-intervention pulse (minute) at the start of the transition phase was assessed.
The rhythmic dilation of an artery that results from beating of the heart. Measurements were made with a heart rate monitor.
pre-intervention respiration (minute) at the start of the transition phase was assessed.
the inhaling of oxygen and the exhaling of carbon dioxide. is found by counting the number of breaths (how many times the chest rises).
post-intervention respiration (minute) at the start of the transition phase was assessed.
the inhaling of oxygen and the exhaling of carbon dioxide. is found by counting the number of breaths (how many times the chest rises).
pre-intervention fetal heart rate (minute) at the start of the transition phase was assessed.
Fetal heart rate was measured using a fetal Doppler device.
post-intervention fetal heart rate (minute) at the start of the transition phase was assessed.
Fetal heart rate was measured using a fetal Doppler device.
pre-intervention contraction frequency (minute) at the start of the transition phase was assessed.
Measurements were made using the NST device.
post-intervention contraction frequency (minute) at the start of the transition phase was assessed.
Measurements were made using the NST device.
pre-intervention contraction duration (minute) at the start of the transiton phase was assessed.
Measurements were made using the NST device.
post-intervention contraction duration (minute) at the start of the transiton phase was assessed.
Measurements were made using the NST device.
pre-intervention contraction severity (minute) at the start of the transition phase was assessed.
Measurements were made using the NST device.
post-intervention contraction severity (minute) at the start of the transition phase was assessed.
Measurements were made using the NST device.

Full Information

First Posted
July 6, 2022
Last Updated
August 8, 2022
Sponsor
Abant Izzet Baysal University
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1. Study Identification

Unique Protocol Identification Number
NCT05495009
Brief Title
Virtual Reality, Labor Pain, Anxiety, Birth Perception
Official Title
Birth Journey Through Virtual Reality :Pain, Anxiety and Birth Perception
Study Type
Interventional

2. Study Status

Record Verification Date
August 2022
Overall Recruitment Status
Completed
Study Start Date
June 21, 2021 (Actual)
Primary Completion Date
December 12, 2021 (Actual)
Study Completion Date
December 12, 2021 (Actual)

3. Sponsor/Collaborators

Responsible Party, by Official Title
Principal Investigator
Name of the Sponsor
Abant Izzet Baysal University

4. Oversight

Studies a U.S. FDA-regulated Drug Product
No
Studies a U.S. FDA-regulated Device Product
No
Data Monitoring Committee
No

5. Study Description

Brief Summary
The research was carried out in a randomized controlled trial to determine the effect of using virtual reality glasses on labor pain, anxiety, and labor perception of pregnant women. 60 pregnant women participated in the study at the Maternity and Children's Hospital located in the city center of Bolu. The data were collected via Introductory information form, Visual Comparison Scale-Pain, Visual Comparison Scale-Anxiety, labor follow-up form, Mother's Perception of Birth Scale, and virtual reality satisfaction evaluation form. Number, percentage, mean, standard deviation, Pearson chi-square, t-test for both groups were used to evaluate the data via the SPSS program. Statistical significance was accepted as p<0.05. Pregnant women in the experimental and control groups were found to be homogeneous in terms of sociodemographic and obstetric characteristics (p>0.05). At the beginning of labor, both pregnant groups showed similar score of the mean pain and anxiety(p>0.05). After applying 20 minutes in the active phase and 10 minutes in the transitional phase, the mean pain and anxiety scores of the experimental group were found to be lower, and this difference was found to be statistically significant(p<0.001). In the postpartum period, it was determined that the birth Perception Scale mean scores of the groups were similar. 90% of the pregnant women reported that they were satisfied with the virtual reality application and 93% of them reported that they would recommend this application. As a result, the use of virtual reality during birth reduces pain and anxiety at birth but does not affect the perception of birth.
Detailed Description
Childbirth is one of the important experiences in a woman's life and this experience is affected by subjective, psychological and physiological processes. While birth is a positive life experience for some women , it is a traumatic and negative experience for others . One of the factors that most affect women who experience many emotions together during the birth process is labor pain. The perception and severity of labor pain, which is part of the normal process, varies from person to person. In the literature, it has been shown that 50-52% of women experience severe labor pain. Severe labor pain may be associated with decreased uteroplacental perfusion, prolongation of labor and labor with intervention, postpartum depression and anxiety by causing an increase in maternal catecholamine levels. This leads to a prolonged hospital stay, difficulty in performing basic activities, and consequently a negative birth experience It also leads women who want to avoid pain to prefer cesarean delivery instead of vaginal delivery. The birth process is also an important source of anxiety in women. Studies have shown that women experience moderate anxiety about childbirth. It is known that anxiety experienced at birth affects the health of the mother, fetus and newborn negatively and increases the severity of labor pain. Pain that comes at frequent and intense intervals increases the anxiety level of the woman, leading to increased tension in the pelvic muscles, fatigue, and inadequate coping with pain . There is a two-way relationship between anxiety and pain in childbirth, and this vicious cycle between anxiety and pain negatively affects the course of labor, reduces the self-confidence of the pregnant woman and causes her to feel helpless and unsuccessful. Pain and anxiety are important factors affecting birth perception and birth outcomes. Effective management of pain and anxiety at birth for a positive birth experience is among the main goals of obstetric care. The most effective strategies for a positive birth experience; It has been reported that creating a positive birth environment, supporting women during childbirth, intrapartum care with minimal intervention, preparation for childbirth, relaxation and pain relief applications . Pharmacological and non-pharmacological methods are used to effectively cope with pain at birth. Pharmacological methods require attention in their use because of their side effects, application limitations, and uncertainties of their effects on the mother and fetus . The use of non-pharmacological methods, which are easy to apply, safe, and have various advantages in ensuring active participation and cooperation of women in the birth process, without using any medication, is becoming more common in pain management. Studies have emphasized that non-pharmacological methods reduce pain and anxiety levels during the birth process, increase maternal satisfaction at birth, and strengthen mother-infant communication. Distraction, focusing and relaxation by daydreaming are among the commonly used non-pharmacological methods in reducing pain. However, since dreaming and daydreaming can be difficult during the birth process, it is recommended to use applications that will facilitate this . For this purpose, virtual reality glasses have been used in recent years. With these glasses, a visual experience environment is created through three-dimensional videos by creating a real-like virtual world for individuals. It has been shown that the clinical use of virtual reality glasses, which can be used in many areas, is useful and reliable. These glasses are used in children during painful invasive procedures, acute and chronic pain management, burn treatments, preoperative anxiety, psychiatric diagnosis and treatment interventions, physical therapy and rehabilitation applications are used. Although virtual reality has been shown to be an effective method in the management of pain and anxiety, studies showing its effect on pain at birth and anxiety are limited. Based on these data, in this study, it was aimed to determine the effect of the video watched by using virtual reality glasses during labor on labor pain, anxiety and labor perception of pregnant women. Research Hypotheses H0 : Watching video with virtual reality glasses has no effect on labor pain, anxiety and birth perception. H1: Watching video with virtual reality glasses has an effect on labor pain. H2: Watching video with virtual reality glasses has an effect on anxiety at birth. H3: Watching a video with virtual reality glasses has an effect on birth perception.

6. Conditions and Keywords

Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Labor Pain, Anxiety
Keywords
labor, pain, anxiety, birth perception, virtual reality

7. Study Design

Primary Purpose
Supportive Care
Study Phase
Not Applicable
Interventional Study Model
Parallel Assignment
Model Description
Randomized controlled experimental research
Masking
None (Open Label)
Allocation
Randomized
Enrollment
60 (Actual)

8. Arms, Groups, and Interventions

Arm Title
Standard of care
Arm Type
No Intervention
Arm Description
Introductory information form (IIF), labor follow-up form (FFL) and VAS-P, VAS-A were filled in the latent phase (1-3 cm). At the beginning of the active (4 cm) and transitional phases (8 cm), FFL, VAS-P and VAS-A were filled and no intervention was applied. 20 min in active phase. then, FFL, VAS-P and VAS-A were filled after 10 min in the transition phase. The Perception of Birth Scale is filled after birth.
Arm Title
Standard of care+ virtual reality glasses
Arm Type
Experimental
Arm Description
Introductory information form (IIF), labor follow-up form (FFL) and VAS-P, VAS-A were filled in the latent phase (1-3 cm). At the beginning of the active (4 cm) and transitional phases (8 cm), after filling FFL, VAS-P and VAS-A, video was watched with virtual reality glasses. 20 minutes in active phase after watching the video. then, FFL, VAS-P and VAS-A were filled after 10 min in the transition phase. After the birth, the Perception of Birth Scale and Virtual Reality Satisfaction Form were filled.
Intervention Type
Other
Intervention Name(s)
Standard of care+virtual reality glasses
Intervention Description
At the beginning of the active and transitional phases of labor, videos were watched with virtual reality glasses.
Primary Outcome Measure Information:
Title
pre-intervention pain at the start of the active phase was assessed by Visual Analogue Scale-Pain (VAS-P)
Description
The scale is a 10 cm ruler that represents painlessness at one end (0=no pain) and the most severe pain (10=severe pain) at the other end. The patient is asked to put a line or mark on the point representing the intensity of pain. The part from the "no pain" point to the point marked by the participant is measured in mm and the value found indicates the patient's pain level.
Time Frame
It was applied before the intervention was performed when the cervical opening was 4 cm.
Title
post-intervention pain at the start of the active phase was assessed Visual Analogue Scale-Pain (VAS-P)
Description
The scale is a 10 cm ruler that represents painlessness at one end (0=no pain) and the most severe pain (10=severe pain) at the other end. The patient is asked to put a line or mark on the point representing the intensity of pain. The part from the "no pain" point to the point marked by the participant is measured in mm and the value found indicates the patient's pain level.
Time Frame
It was applied after the intervention was performed when the cervical opening was 4 cm.
Title
pre-intervention anxiety at the start of the active phase was assessed by Visual Analogue Scale-Anxiety (VAS-A)
Description
The scale is a 10 cm ruler representing the absence of anxiety (0 = no anxiety) at one end and the most severe anxiety (10 = severe anxiety) at the other end. The patient is asked to put a line or mark on the area showing the level of anxiety. The part from the no anxiety point to the point marked by the patient is measured in mm and the value found indicates the patient's anxiety level.
Time Frame
It was applied before the intervention was performed when the cervical opening was 4 cm.
Title
post-intervention anxiety at the start of the active phase was assessed by Visual Analogue Scale-Anxiety (VAS-A)
Description
The scale is a 10 cm ruler representing the absence of anxiety (0 = no anxiety) at one end and the most severe anxiety (10 = severe anxiety) at the other end. The patient is asked to put a line or mark on the area showing the level of anxiety. The part from the no anxiety point to the point marked by the patient is measured in mm and the value found indicates the patient's anxiety level.
Time Frame
It was applied after the intervention was performed when the cervical opening was 4 cm.
Title
pre-intervention pain at the start of the transition phase was assessed by Visual Analogue Scale-Pain (VAS-P)
Description
The scale is a 10 cm ruler that represents painlessness at one end (0=no pain) and the most severe pain (10=severe pain) at the other end. The patient is asked to put a line or mark on the point representing the intensity of pain. The part from the "no pain" point to the point marked by the participant is measured in mm and the value found indicates the patient's pain level.
Time Frame
It was applied before the intervention was performed when the cervical opening was 8 cm.
Title
post-intervention pain at the start of the transition phase was assessed by Visual Analogue Scale-Pain (VAS-P)
Description
The scale is a 10 cm ruler that represents painlessness at one end (0=no pain) and the most severe pain (10=severe pain) at the other end. The patient is asked to put a line or mark on the point representing the intensity of pain. The part from the "no pain" point to the point marked by the participant is measured in mm and the value found indicates the patient's pain level.
Time Frame
It was applied after the intervention was performed when the cervical opening was 8 cm.
Title
pre-intervention anxiety at the start of the transition phase was assessed by Visual Analogue Scale-Anxiety (VAS-A)
Description
The scale is a 10 cm ruler representing the absence of anxiety (0 = no anxiety) at one end and the most severe anxiety (10 = severe anxiety) at the other end. The patient is asked to put a line or mark on the area showing the level of anxiety. The part from the no anxiety point to the point marked by the patient is measured in mm and the value found indicates the patient's anxiety level.
Time Frame
It was applied before the intervention was performed when the cervical opening was 8 cm.
Title
post-intervention anxiety at the start of the transition phase was assessed by Visual Analogue Scale-Anxiety (VAS-A)
Description
The scale is a 10 cm ruler representing the absence of anxiety (0 = no anxiety) at one end and the most severe anxiety (10 = severe anxiety) at the other end. The patient is asked to put a line or mark on the area showing the level of anxiety. The part from the no anxiety point to the point marked by the patient is measured in mm and the value found indicates the patient's anxiety level.
Time Frame
It was applied after the intervention was performed when the cervical opening was 8 cm.
Title
birth perception in the postpartum period was assessed by Mother's Perception of Birth Scale
Description
The Mother's Perception of Birth Scale, which evaluates the experiences and perceptions of mothers at the time of birth, was developed by Fawcett and Knauth (144). The Turkish validity and reliability study of the scale was carried out by Güngör and Beji (2007). Experiences at the time of birth (7 items; 3, 5, 6, 8, 15, 17, 18), experiences during the pain period of labor (7 items; 1, 2, 4, 7, 9, 10, 16), postpartum (4 items) It consists of a total of 5 sub-dimensions and 25 items, namely; 22, 23, 24, 25), partner involvement (4 items; 11,12,20,21) and awareness (3 items; 13,14,19). Each item is scored from 1 to 5 in the Mother's Perception of Birth Scale. It is evaluated as 1-Not at all, 2-A little, 3-Moderate, 4-Very, 5-Very much. Since the questions 15-16-17-18-19 of the scale contain negative statements, scoring is done in reverse for these questions.
Time Frame
postpartum 4 hour
Secondary Outcome Measure Information:
Title
pre-intervention systolic blood pressure (mmHg) at the start of the active phase was assessed.
Description
systolic blood pressure, measures the pressure in your arteries when your heart beats. Measurements were made with a blood pressure monitor.
Time Frame
It was applied before the intervention was performed when the cervical opening was 4 cm.
Title
post-intervention systolic blood pressure (mmHg) at the start of the active phase was assessed.
Description
systolic blood pressure, measures the pressure in your arteries when your heart beats. Measurements were made with a blood pressure monitor.
Time Frame
It was applied after the intervention was performed when the cervical opening was 4 cm.
Title
pre-intervention diastolic blood pressure (mmHg) at the start of the active phase was assessed.
Description
diastolic blood pressure, measures the pressure in your arteries when your heart rests between beats. Measurements were made with a blood pressure monitor.
Time Frame
It was applied before the intervention was performed when the cervical opening was 4 cm.
Title
post-intervention diastolic blood pressure (mmHg) at the start of the active phase was assessed.
Description
diastolic blood pressure, measures the pressure in your arteries when your heart rests between beats. Measurements were made with a blood pressure monitor.
Time Frame
It was applied after the intervention was performed when the cervical opening was 4 cm.
Title
pre-intervention pulse (minute) at the start of the active phase was assessed.
Description
The rhythmic dilation of an artery that results from beating of the heart. Measurements were made with a heart rate monitor.
Time Frame
It was applied before the intervention was performed when the cervical opening was 4 cm.
Title
post-intervention pulse (minute) at the start of the active phase was assessed.
Description
The rhythmic dilation of an artery that results from beating of the heart. Measurements were made with a heart rate monitor.
Time Frame
It was applied after the intervention was performed when the cervical opening was 4 cm.
Title
pre-intervention respiration (minute) at the start of the active phase was assessed.
Description
the inhaling of oxygen and the exhaling of carbon dioxide. is found by counting the number of breaths (how many times the chest rises).
Time Frame
It was applied before the intervention was performed when the cervical opening was 4 cm.
Title
post-intervention respiration (minute) at the start of the active phase was assessed.
Description
the inhaling of oxygen and the exhaling of carbon dioxide. is found by counting the number of breaths (how many times the chest rises).
Time Frame
It was applied after the intervention was performed when the cervical opening was 4 cm.
Title
pre-intervention fetal heart rate (minute) at the start of the active phase was assessed.
Description
Fetal heart rate was measured using a fetal Doppler device.
Time Frame
It was applied before the intervention was performed when the cervical opening was 4 cm.
Title
post-intervention fetal heart rate (minute) at the start of the active phase was assessed.
Description
Fetal heart rate was measured using a fetal Doppler device.
Time Frame
It was applied after the intervention was performed when the cervical opening was 4 cm.
Title
pre-intervention contraction frequency (minute) at the start of the active phase was assessed.
Description
Measurements were made using the NST device.
Time Frame
It was applied before the intervention was performed when the cervical opening was 4 cm.
Title
post-intervention contraction frequency (minute) at the start of the active phase was assessed.
Description
Measurements were made using the NST device.
Time Frame
It was applied after the intervention was performed when the cervical opening was 4 cm.
Title
pre-intervention contraction duration (minute) at the start of the active phase was assessed.
Description
Measurements were made using the NST device.
Time Frame
It was applied before the intervention was performed when the cervical opening was 4 cm.
Title
post-intervention contraction duration (minute) at the start of the active phase was assessed.
Description
Measurements were made using the NST device.
Time Frame
It was applied after the intervention was performed when the cervical opening was 4 cm.
Title
pre-intervention contraction severity (minute) at the start of the active phase was assessed.
Description
Measurements were made using the NST device.
Time Frame
It was applied before the intervention was performed when the cervical opening was 4 cm.
Title
post-intervention contraction severity (minute) at the start of the active phase was assessed.
Description
Measurements were made using the NST device.
Time Frame
It was applied after the intervention was performed when the cervical opening was 4 cm.
Title
pre-intervention systolic blood pressure (mmHg) at the start of the transition phase was assessed.
Description
systolic blood pressure, measures the pressure in your arteries when your heart beats. Measurements were made with a blood pressure monitor.
Time Frame
It was applied before the intervention was performed when the cervical opening was 8 cm.
Title
post-intervention systolic blood pressure (mmHg) at the start of the transition phase was assessed.
Description
systolic blood pressure, measures the pressure in your arteries when your heart beats. Measurements were made with a blood pressure monitor.
Time Frame
It was applied after the intervention was performed when the cervical opening was 8 cm.
Title
pre-intervention diastolic blood pressure (mmHg) at the start of the transition phase was assessed.
Description
diastolic blood pressure, measures the pressure in your arteries when your heart rests
Time Frame
It was applied before the intervention was performed when the cervical opening was 8 cm.
Title
post-intervention diastolic blood pressure (mmHg) at the start of the transition phase was assessed.
Description
diastolic blood pressure, measures the pressure in your arteries when your heart rests
Time Frame
It was applied after the intervention was performed when the cervical opening was 8 cm.
Title
pre-intervention pulse (minute) at the start of the transition phase was assessed.
Description
The rhythmic dilation of an artery that results from beating of the heart. Measurements were made with a heart rate monitor.
Time Frame
It was applied before the intervention was performed when the cervical opening was 8 cm.
Title
post-intervention pulse (minute) at the start of the transition phase was assessed.
Description
The rhythmic dilation of an artery that results from beating of the heart. Measurements were made with a heart rate monitor.
Time Frame
It was applied after the intervention was performed when the cervical opening was 8 cm.
Title
pre-intervention respiration (minute) at the start of the transition phase was assessed.
Description
the inhaling of oxygen and the exhaling of carbon dioxide. is found by counting the number of breaths (how many times the chest rises).
Time Frame
It was applied before the intervention was performed when the cervical opening was 8 cm.
Title
post-intervention respiration (minute) at the start of the transition phase was assessed.
Description
the inhaling of oxygen and the exhaling of carbon dioxide. is found by counting the number of breaths (how many times the chest rises).
Time Frame
It was applied after the intervention was performed when the cervical opening was 8 cm.
Title
pre-intervention fetal heart rate (minute) at the start of the transition phase was assessed.
Description
Fetal heart rate was measured using a fetal Doppler device.
Time Frame
It was applied before the intervention was performed when the cervical opening was 8 cm.
Title
post-intervention fetal heart rate (minute) at the start of the transition phase was assessed.
Description
Fetal heart rate was measured using a fetal Doppler device.
Time Frame
It was applied after the intervention was performed when the cervical opening was 8 cm.
Title
pre-intervention contraction frequency (minute) at the start of the transition phase was assessed.
Description
Measurements were made using the NST device.
Time Frame
It was applied before the intervention was performed when the cervical opening was 8 cm.
Title
post-intervention contraction frequency (minute) at the start of the transition phase was assessed.
Description
Measurements were made using the NST device.
Time Frame
It was applied after the intervention was performed when the cervical opening was 8 cm.
Title
pre-intervention contraction duration (minute) at the start of the transiton phase was assessed.
Description
Measurements were made using the NST device.
Time Frame
It was applied before the intervention was performed when the cervical opening was 8 cm.
Title
post-intervention contraction duration (minute) at the start of the transiton phase was assessed.
Description
Measurements were made using the NST device.
Time Frame
It was applied after the intervention was performed when the cervical opening was 8 cm.
Title
pre-intervention contraction severity (minute) at the start of the transition phase was assessed.
Description
Measurements were made using the NST device.
Time Frame
It was applied before the intervention was performed when the cervical opening was 8 cm.
Title
post-intervention contraction severity (minute) at the start of the transition phase was assessed.
Description
Measurements were made using the NST device.
Time Frame
It was applied after the intervention was performed when the cervical opening was 8 cm.

10. Eligibility

Sex
Female
Gender Based
Yes
Gender Eligibility Description
The study was carried out with women in accordance with the subject of the study.
Minimum Age & Unit of Time
18 Years
Maximum Age & Unit of Time
35 Years
Accepts Healthy Volunteers
Accepts Healthy Volunteers
Eligibility Criteria
Inclusion Criteria: Able to communicate verbally Between the ages of 18-35 No pregnancy-related risk diagnosis, Primiparous, Vaginal delivery planned, Gestational week is between 37-42, Single, live fetus and head presentation, In the latent phase (1-3 cm) on admission to the delivery room, Not having any dystocia that may affect the duration of labor (placental dystocia, pelvic dystocia, etc.). No induction, No epidural anaesthesia. Pregnant women without vision and hearing problems were included in the study. Exclusion Criteria: Refusing to participate in the research, Diagnosed with risky pregnancy, Watching the video in active phase for less than 20 minutes Watching the video in transition phase for less than 10 minutes Cesarean section Pregnant women who used any pharmacological analgesia were not included in the study.
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
Mervenur BÖYÜK
Organizational Affiliation
Baibu
Official's Role
Principal Investigator
Facility Information:
Facility Name
İzzet Baysal State Hospital, Obstetrics and Pediatrics Unit, delivery room service
City
Bolu
State/Province
Center
ZIP/Postal Code
14280
Country
Turkey

12. IPD Sharing Statement

Learn more about this trial

Virtual Reality, Labor Pain, Anxiety, Birth Perception

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