Skip to content

Effects of Virtual Reality Application and Progressive Relaxation Exercise

Effects of Virtual Reality Application and Progressive Relaxation Exercise Training on Pregnant Women's Stress, Birth Affect and Birth Self-Efficacy

Status
Not yet recruiting
Phases
NA
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT06896955
Enrollment
75
Registered
2025-03-26
Start date
2025-03-25
Completion date
2026-03-25
Last updated
2025-03-26

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

Conditions

Exercise, Pregnancy, Virtual Reality

Keywords

Pregnancy, Exercise, progressive exercise, virtual reality

Brief summary

In the study, random assignment and randomization concealment will be applied to control selection bias. Pregnant women were assigned to groups by an independent statistician using the block randomization method. For this purpose, 6-digit combinations consisting of the letters A, B and C were first created in the randomization of 78 women.

Detailed description

There will be three groups in the randomized experimental controlled study:PRE (Progressive Relaxation Exercise), VR (Virtual Reality)+PGR (Progressive Relaxation Exercise) and Control group. In order to carry out the application phase of the study, the responsible researcher participated in the training program on PRE and received a certificate on this subject. In addition, permission for the use of PRE Cd was obtained from the Turkish Psychologists Association to be used in the PRE group. The following procedures will be performed for pregnant women included in the study.

Interventions

OTHERPMR+VR Education

PMR and VR education

OTHERPMR Education

PMR education

Sponsors

Cukurova University
Lead SponsorOTHER

Study design

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

Eligibility

Sex/Gender
FEMALE
Age
18 Years to No maximum
Healthy volunteers
Yes

Inclusion criteria

* Voluntary participation * No communication difficulties (no mental retardation, no visual/hearing impairment) * Knowing Turkish and being literate * No fetal anomalies * Being in the 32nd week of pregnancy * Not being diagnosed with a risky pregnancy (multiple pregnancy, premature rupture of membranes, preeclampsia, gestational diabetes, placenta previa, etc., pregnancies may end with a cesarean section)

Exclusion criteria

* Having a psychiatric disease diagnosis

Design outcomes

Primary

MeasureTime frameDescription
Pregnancy Stress Assessment Scalepre-intervention, after 2 monthChange in pregnancy-related stress levels in pregnant women. As the score from the scale increases, stress increases.
Birth Self-Efficacy Scaleintervention after 2 monthChange in self-efficacy levels of pregnant women during labor. As the score from the scale increases, self-efficacy increases.
Birth Affect Scaleintervention after 2 monthChange in the emotional state experienced by mothers during labor. As the score from the scale increases, positive affect increases.

Countries

Turkey (Türkiye)

Contacts

Primary ContactSule Gokyildiz Surucu, Prof.
gokyildizsurucu@gmail.com+90 (322) 338 64 84
Backup ContactSenay Dagilgan, Msc
sdagilgan@cu.edu.tr+90 (322) 338 65 38

Outcome results

None listed

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