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Virtual Reality-Enabled Digital Storytelling

Evaluation of the Effects of Digital Storytelling Applied to Primiparous Pregnant Women With Virtual Reality Glasses on Prenatal Attachment, Fear of Childbirth, Perception of Childbirth Self-Efficacy, and Non-Stress Test Results

Status
Not yet recruiting
Phases
NA
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT07167030
Enrollment
112
Registered
2025-09-11
Start date
2025-11-01
Completion date
2026-12-30
Last updated
2025-09-16

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Primiparous Pregnant Women

Keywords

Prenatal attachment, Fear of Childbirth, Birth Self-Efficacy, Virtual Reality, Digital Storytelling

Brief summary

Current scientific literature on VR details primarily focuses on fear and anxiety during childbirth. Variables such as attachment, fear, and self-efficacy are often considered independently. Therefore, in addition to interventions focused on the prenatal period, a need arose for holistic audiovisual and technologically supported intervention models that simultaneously address multidimensional aspects of life, such as prenatal attachment, fear of childbirth, and perception of childbirth self-efficacy.

Detailed description

This study is a randomized controlled trial conducted to evaluate the effects of digital storytelling applied to primiparous pregnant women via virtual reality glasses on prenatal attachment, fear of childbirth, perception of childbirth self-efficacy, and non-stress test results. The study will consist of two groups: an experimental and a control group. Participants in the experimental group will access a digital storytelling training program via virtual reality glasses and receive information and guidance on topics such as prenatal attachment, fear of childbirth, and perception of childbirth self-efficacy. Participants in the control group will receive standard care.

Interventions

BEHAVIORALVirtual Reality Digital Storytelling

Participants in the intervention group will receive digital storytelling modules using virtual reality (VR) headsets once a week for four weeks, starting at 28 weeks of gestation. Each module will include three topics (2-10 minutes). After each topic, there will be a rest period followed by an interactive session. The final two modules will be administered during the NST recording, and mother and baby status will be monitored. Each module, including the interactive session, will last 45-50 minutes. Participants will receive an educational brochure after the module and will be reminded via WhatsApp.

Sponsors

Bozok University
Lead SponsorOTHER

Study design

Allocation
RANDOMIZED
Intervention model
PARALLEL
Primary purpose
SUPPORTIVE_CARE
Masking
SINGLE (Subject)

Masking description

There is no other hidden side to this study.

Intervention model description

Arm 1 Intervention Arm: Participants in the intervention group will receive digital storytelling modules using virtual reality (VR) headsets once a week for four weeks, starting at 28 weeks of gestation. Each module will include three topics (2-10 minutes). After each topic, there will be a rest period followed by an interactive session. The final two modules will be administered during the NST recording, and mother and baby status will be monitored. Each module, including the interactive session, will last 45-50 minutes. Participants will receive an educational brochure after the module and will be reminded via WhatsApp. Arm 2 Control Arm: Participants in the control group will receive routine care. Posttests (at the end of 36 weeks of gestation): * Prenatal Attachment Inventory * Wijma Birth Expectations/Experiences Questionnaire Version A * Short Version of the Labor Self-Efficacy Scale * Satisfaction Level Information Form for the VR Headset Application * NST Follow-up Form * Video

Eligibility

Sex/Gender
FEMALE
Age
18 Years to 40 Years
Healthy volunteers
Yes

Inclusion criteria

* Primiparous women in their 28th week of pregnancy * Between the ages of 18 and 40 * Experiencing a singleton pregnancy * Applied to the Yozgat City Hospital Gynecology and Obstetrics Clinic and agreed to participate in the study * Have a primary school education and can understand Turkish * Have no serious vision or balance problems that would prevent the use of VR glasses * Have not experienced any risky pregnancy problems (premature membrane rupture, preeclampsia, gestational diabetes, etc.) * Have no identified fetal anomalies * Have no psychiatric diagnosis

Exclusion criteria

* Pregnant women who cannot obtain a work permit and who do not agree to participate in the study will not be included in the study.

Design outcomes

Primary

MeasureTime frameDescription
Prenatal Attachment InventoryTime Frame: Pre-test (before intervention) Time Frame: Post-test (after intervention: 36th week of pregnancy, after the fourth module)The Prenatal Attachment Inventory (PAI) developed by Muller (1993) is used to assess the thoughts, feelings, and states experienced by women during pregnancy and to determine their attachment to their babies during the prenatal period (Muller, 1993). The Turkish validity and reliability study of the inventory, conducted by Yılmaz and Beji (2013), consists of 21 items. Each item is a four-point Likert-type scale, ranging from 1 to 4. A minimum score of 21 and a maximum score of 84 can be obtained from the scale. Increasing scores indicate increased attachment. The scale's validity and reliability performance was found to be 0.84, with a Cronbach's alpha of 0.10.
Wijma Childbirth Expectation/Experience Questionnaire Version A (W-DEQ-A)Time Frame: Pre-test (before intervention) Time Frame: Post-test (after intervention: 36th week of pregnancy, after the fourth module)Developed by Wijma et al. (1998) to assess the level of fear of childbirth experienced by pregnant women, the scale was adapted into Turkish by Körükcü (2009). Version A of the W-DEQ is a 33-item scale. Responses are numbered from 0 to 5 and are on a six-point Likert-type scale. The minimum score is 0, and the maximum score is 165. A high total score indicates a high level of fear. In the validity and reliability study of the scale, Cronbach's Alpha was found to be 0.89 (Körükcü, 2009).
Short Version of the Labor Self-Efficacy ScaleTime Frame: Pre-test (before intervention) Time Frame: Post-test (after intervention: 36th week of pregnancy, after the fourth module)The Turkish adaptation of the scale, developed to measure women's self-efficacy for childbirth, was conducted by Ersoy (2011). The scale consists of two sub-dimensions: competence and outcome expectation, and a total of 32 questions. Scores for each sub-dimension range from 16 to 160. As the score on each sub-dimension increases, the competence and outcome expectation for childbirth increases. The Likert-type scale is scored from 1 to 10. In the outcome expectation sub-dimension of the scale, 1 represents not at all useful, and 10 represents very useful. In the competence expectation sub-dimension, questions 1 to 13 are scored as 1 completely confident, 10 represents not at all confident, and the remaining questions are scored as 1 not at all confident, and 10 represents completely confident. The first 13 questions in the competence expectation sub-dimension of the scale are reverse-scored. The total score obtained from the scale ranges from 32 to 320. As the score on the

Secondary

MeasureTime frameDescription
NST Follow-up FormTime Frame: 34th weeks of pregnancy (during the last two modules) Time Frame: 36th weeks of pregnancy (during the last two modules)This form consists of sections containing the emotional state and NST findings experienced by pregnant women during the NST procedure. The NST results in the NST Follow-up Form will be evaluated and recorded by the researcher.

Other

MeasureTime frameDescription
Video Immersion Scale (VIS)Time Frame: Post-intervention (post-intervention: 36th week of pregnancy, after the fourth module)The Video Immersion Scale, developed by Visser et al. (2016), was adapted into Turkish by Deryakulu et al. (2019). The scale consists of five factors and a total of 15 items. The Cronbach's alpha internal consistency coefficients calculated for the subfactors and the entirety of the Video Immersion Scale, which is a seven-point Likert-type scale, are as follows: Factor 1 (Attention) 0.57; Factor 2 (Narrative World Immersion) 0.73; Factor 3 (Identity) 0.87; Factor 4 (Empathy) 0.78; Factor 5 (Emotion) 0.69; and for the entire scale, 0.90. In this study, the Cronbach's alpha reliability coefficients for the factors were, respectively, Factor 1 (Attention) 0.57; Factor 2 (Entering the narrative world) was calculated as 0.71; Factor 3 (Identity) as 0.70; Factor 4 (Empathy) as 0.72; Factor 5 (Emotion) as 0.78; and 0.81 for the entire scale.
Virtual Reality Glasses Application Satisfaction Level Information FormTime Frame: Post-intervention (post-intervention: 36th week of pregnancy, after the fourth module)This form will include questions prepared by researchers to determine satisfaction with the video watched with virtual reality glasses.

Contacts

Primary ContactRUKİYE DİKMEN, PhD Student
rukiye.dikmen@yobu.edu.tr+905433686510

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 4, 2026