Pain Perceived by Women During Episiotomy Repair
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ClinicalTrials.gov Identifier: NCT05134376 |
Recruitment Status :
Completed
First Posted : November 24, 2021
Last Update Posted : November 24, 2021
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This research was carried out to evaluate the effect of video and accompanying music played with virtual reality glasses during episiotomy repair on women's perceived pain, vital signs and postpartum comfort during episiotomy repair.
This research is a randomized controlled experimental study. The study was conducted on 84 pregnant women, 40 of whom were in the intervention group and 44 were in the control group.
The goals expected to be achieved during the research are; Reducing the perceived pain during episiotomy repair with video and accompanying music played with virtual reality glasses during episiotomy repair Video and accompanying music watched with virtual reality glasses during episiotomy repair increase postpartum comfort The positive effect of video and accompanying music on vital signs during episiotomy repair with virtual reality glasses
Condition or disease | Intervention/treatment | Phase |
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Virtual Reality Birth | Other: During Episiotomy Repair, Women Will Be Watching Virtual Reality Glasses Accompanied by Music | Not Applicable |
Workgroup implementation steps Informed Voluntary Consent Form and Pregnancy Introductory Form (the first 8 questions of the pregnant introductory information - labor and episiotomy follow-up form) will be filled in by the researcher, to the pregnant women who were randomized daily to the study and control group by going to the clinic during the research. During the repair of mediolateral episiotomy, the pregnant women included in the study group will be shown the video accompanying the acemaşîrân makam with sterile virtual reality glasses with a view of nature. In the literature, it is stated that the video watched with the acemaşîrân makam and virtual reality glasses reduces pain [6, 7, 21] After the internet connection is established with a smart phone, the video to be clicked on youtube.com will be clicked, Relaxation Project 1 (SBS VR) video and Acemaşiran Ayini Şerifi Ney-Bendir will be selected for the sound, and video and music will be played with virtual reality glasses by pressing the play button[22, 23] Sound and image will be adjusted as the pregnant woman wants. During the study, all pregnant women included in the study will be given the same care and follow-up, apart from watching the video. The video containing nature scenes prepared by the researcher and the acemaşîrân maqam will be watched from the moment the episiotomy is opened to the time when the episiotomy is closed. Numerical pain assessment scale will be applied before, during (during hymen suturing) and 1 hour after the end of mediolateral episiotomy repair. Postpartum comfort scale 4-24th postpartum. The vital signs of the pregnant women in the study group will be recorded by the researcher before and during episiotomy repair (during hymen suturing) and 1 hour after the end of mediolateral episiotomy repair. In episiotomy repair, the time from the first suture to the last column will be recorded. The pregnant woman will be asked how long she perceives the duration of episiotomy.
Control group application steps Unlike the experimental group, only video and music applications will not be applied to the pregnant women included in the control group. Other applications will be made in the same way.
Study Type : | Interventional (Clinical Trial) |
Actual Enrollment : | 84 participants |
Allocation: | Randomized |
Intervention Model: | Parallel Assignment |
Intervention Model Description: | This research is a randomized controlled experimental study. |
Masking: | None (Open Label) |
Masking Description: | episiotomy application and intervention was done by midwives |
Primary Purpose: | Supportive Care |
Official Title: | The Effect of Virtual Reality Glasses Watched With Music on Pain Perceived by Women During Episiotomy Repair, Vital Signs and Postpartum Comfort |
Actual Study Start Date : | November 1, 2020 |
Actual Primary Completion Date : | January 31, 2021 |
Actual Study Completion Date : | January 31, 2021 |
Arm | Intervention/treatment |
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Experimental: Workgroup
During the repair of the mediolateral episiotomy, the pregnant women included in the study group will be shown a video accompanying the acemaşîrân office with sterile virtual reality glasses with a view of nature.
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Other: During Episiotomy Repair, Women Will Be Watching Virtual Reality Glasses Accompanied by Music
Unlike the experimental group, only video and music application will not be applied to the pregnant women included in the control group. Other applications will be done exactly. |
No Intervention: Control
Unlike the experimental group, only video and music applications will not be applied to the pregnant women included in the control group. Other applications will be done in the same way.
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- Numerical Pain Rating Scale [ Time Frame: before the episiotomy intervention, ]In the numerical evaluation scale, pain ranges from 0 (absence of pain) to 10 (unbearable pain).
- Numerical Pain Rating Scale [ Time Frame: during the hymen suturing during the episiotomy, ]In the numerical evaluation scale, pain ranges from 0 (absence of pain) to 10 (unbearable pain).
- Numerical Pain Rating Scale [ Time Frame: one hour after the intervention. ]In the numerical evaluation scale, pain ranges from 0 (absence of pain) to 10 (unbearable pain).
- Postpartum Comfort Scale [ Time Frame: after 24 hours ]The lowest score to be taken on the scale is 34, and the highest score is 170.
- Systolic Blood Pressure [ Time Frame: before the episiotomy intervention, ]mmHg;
- diastolic Blood Pressure [ Time Frame: before the episiotomy intervention, ]mmHg;
- Systolic Blood Pressure [ Time Frame: during the hymen suturing during the episiotomy, ]mmHg;
- diastolic Blood Pressure [ Time Frame: during the hymen suturing during the episiotomy, n ]mmHg;
- Systolic Blood Pressure [ Time Frame: one hour after the intervention ]mmHg;
- diastolic Blood Pressure [ Time Frame: one hour after the intervention ]mmHg;
- pulse, [ Time Frame: before the episiotomy intervention, during the hymen suturing during the episiotomy, and one hour after the intervention ]minute;
- espiratory rate [ Time Frame: before the episiotomy intervention, ]unit
- espiratory rate [ Time Frame: during the hymen suturing during the episiotomy, ]unit
- espiratory rate [ Time Frame: one hour after the intervention ]unit

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Ages Eligible for Study: | 18 Years to 35 Years (Adult) |
Sexes Eligible for Study: | Female |
Gender Based Eligibility: | Yes |
Gender Eligibility Description: | primipary |
Accepts Healthy Volunteers: | Yes |
Inclusion Criteria:
- Turkish,
- 18 - 35 years
- primiparous,
- gestational week 37- 42
- Mediolateral episiotomy performed
- pregnant women in active phase Exclusion Criteria
- high risk pregnancy
- vision and hearing problem
- with deep laceration
- 3rd and 4th degree laceration

To learn more about this study, you or your doctor may contact the study research staff using the contact information provided by the sponsor.
Please refer to this study by its ClinicalTrials.gov identifier (NCT number): NCT05134376
Turkey | |
Adnan Menderes University Institute of Health Sciences ile | |
Aydın, Turkey |
Study Director: | mine gökduman keleş, 1 |
Responsible Party: | Mine Gokduman Keles, Head of Otolaryngology, Aydin Adnan Menderes University |
ClinicalTrials.gov Identifier: | NCT05134376 |
Other Study ID Numbers: |
AYDIN ADNAN MENDERES UNUVERSTY |
First Posted: | November 24, 2021 Key Record Dates |
Last Update Posted: | November 24, 2021 |
Last Verified: | November 2021 |
Individual Participant Data (IPD) Sharing Statement: | |
Plan to Share IPD: | No |
Studies a U.S. FDA-regulated Drug Product: | No |
Studies a U.S. FDA-regulated Device Product: | No |
Virtual Reality labor pain episiotomy |