Effects of Virtual Reality Application and Progressive Relaxation Exercise
Trial statusNot yet recruiting
Trial phaseNot applicable
Trial typeInterventional
Biological sexFemale
Age18+
SponsorCukurova University
About this trial
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.
Eligibility criteria
This trial accepts healthy volunteersQualifiers
Voluntary participation
No communication difficulties (no mental retardation, no visual/hearing impairment)
Knowing Turkish and being literate
No fetal anomalies
Disqualifiers
Having a psychiatric disease diagnosis
Trial design
Design model
Parallel
Treatments tested in this trial
PMR+VR Education
Other interventionPMR and VR education
PMR Education
Other interventionPMR education
Treatment groups
75 Participants
are divided into 3 treatment groupsGroup A: PMR GroupExperimental treatment 1 intervention
Group B: VR+PMR GroupExperimental treatment 1 intervention
Group C: Control GroupNo intervention 0 interventions
Trial outcomes
Primary outcomes
1
Pregnancy Stress Assessment Scale
Change in pregnancy-related stress levels in pregnant women. As the score from the scale increases, stress increases.
Time frame
pre-intervention, after 2 month2
Birth Self-Efficacy Scale
Change in self-efficacy levels of pregnant women during labor. As the score from the scale increases, self-efficacy increases.
Time frame
intervention after 2 month3
Birth Affect Scale
Change in the emotional state experienced by mothers during labor. As the score from the scale increases, positive affect increases.
Time frame
intervention after 2 monthSponsors and contacts
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Source ClinicalTrials.gov
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