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The Effect of vırtual realıty on paın and Sleep qualıty ın Women
The Effect of vıdeo Watched wıth musıc Through vırtual realıty Glasses and musıc lıstenıng Alone on paın and Sleep qualıty ın Women wıth Dysmenorrhea
The aim of this study is to determine whether a video viewed through virtual reality goggles accompanied by music has an effect on pain and sleep quality in women with dysmenorrhea. The main questions it seeks to answer are as follows:
- Does watching a video through virtual reality goggles accompanied by music reduce pain in women with dysmenorrhea?
- Does watching a video through virtual reality goggles accompanied by music improve sleep quality in women with dysmenorrhea? The study will compare a group that uses music from the virtual reality video with another group to determine whether the virtual reality application has an effect on pain and sleep quality.
Participants will do the following:
For 3 days, use the virtual reality or music application every evening before going to bed after completing the VAS. The next day, after waking up, complete the VAS and the sleep quality scale and record the results.
Studie Overzicht
Studietype
Inschrijving (Werkelijk)
Fase
- Niet toepasbaar
Contacten en locaties
Studie Locaties
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Baykan
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Siirt, Baykan, Turkije (Türkiye), 56460
- Baykan State Hospital
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Deelname Criteria
Geschiktheidscriteria
Leeftijden die in aanmerking komen voor studie
- Kind
- Volwassen
Accepteert gezonde vrijwilligers
Beschrijving
Inclusion Criteria:
- Women who volunteered to participate in the study,
- Who are at least literate,
- Aged 15-49 and not yet in menopause,
- Who are not pregnant,
- Who have been diagnosed with dysmenorrhea by a physician and have a pain intensity of at least 4 on the Visual Analogue Scale
Exclusion Criteria:
- Women with dysmenorrhea pain intensity below 4 on the Visual Analog Scale,
- Women with vision or hearing impairments,
- Women who are unwilling to participate in the study,
- Women using analgesic medications for menstrual pain,
- Pregnant women
Studie plan
Hoe is de studie opgezet?
Ontwerpdetails
- Primair doel: Ondersteunende zorg
- Toewijzing: Gerandomiseerd
- Interventioneel model: Parallelle opdracht
- Masker: Verviervoudigen
Wapens en interventies
Deelnemersgroep / Arm |
Interventie / Behandeling |
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Experimenteel: experiment
Group shown a video using a virtual reality headset: For this experiment, a video featuring nature scenes and waterfalls was downloaded to a phone, loaded into a virtual reality headset, and provided to the participant ready for use.
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Group shown a video using a virtual reality headset: A video containing images of nature and waterfalls is downloaded to a phone and provided to the participant ready to use inside a virtual reality headset; the procedure is carried out as described below. For three consecutive days, each day:
After the study was completed, the equipment returned to the researcher was calibrated and cleaned as necessary by the researcher and prepared for use with another patient.
Andere namen:
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Placebo-vergelijker: control
Unlike the intervention group, the women in the control group were given MP3 players by the researcher, instructed on how to use them, and had the music used in the virtual reality video loaded onto the devices for them to listen to.
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Unlike the intervention group, the women in the control group were given an MP3 player by the researcher, instructed on how to use it, and had the music used in the virtual reality video loaded onto it for them to listen to. For three consecutive days, each day:
After the study was completed, the equipment returned to the researcher was calibrated and cleaned as necessary by the researcher and prepared for use with another patient.
Andere namen:
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Wat meet het onderzoek?
Primaire uitkomstmaten
Uitkomstmaat |
Maatregel Beschrijving |
Tijdsspanne |
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Distribution of women according to the characteristics of their menstrual cycles
Tijdsspanne: 4 weeks
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This table includes the latest menstrual pain scale, the occurrence of pain during the menstrual cycle, the type of dysmenorrhea, the timing of dysmenorrhea, information about menstruation, who provided information about menstruation, the use of pain relievers during the menstrual period, non-pharmacological interventions used to alleviate menstrual pain, non-pharmacological interventions used to alleviate menstrual pain, the presence of dysmenorrhea in the family, and gynecological diagnosis data.
Patients with a pain scale (VAS) score of 4 or higher were evaluated, and the analysis proceeded to secondary outcomes.
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4 weeks
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Secundaire uitkomstmaten
Uitkomstmaat |
Maatregel Beschrijving |
Tijdsspanne |
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Comparison of Participants' Sociodemographic Characteristics by Group
Tijdsspanne: 2 weeks
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This table presents sociodemographic data such as women's marital status, age, and chronic conditions.
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2 weeks
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A Comparison of Certain Characteristics of Participants' Menstrual Cycles Across Groups
Tijdsspanne: 4 weeks
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This table presents data such as the age at first menstruation, menstrual cycle length, and duration of menstrual bleeding
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4 weeks
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Comparison of Dysmenorrhea Characteristics Among Participants by Group
Tijdsspanne: 4 weeks
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This table examines data such as the onset of dysmenorrhea, the presence of dysmenorrhea in the family, the family history of dysmenorrhea, the severity of pain during menstruation, and the use of pain relievers during menstruation.
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4 weeks
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Comparison of Participants' Sleep-Related Characteristics by Group
Tijdsspanne: 4 weeks
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This table provides information on a woman's sleep patterns during her menstrual cycle
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4 weeks
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Comparisons of Participants' Visual Analog Scale (VAS) Scores Between and Within Groups
Tijdsspanne: 6 weeks
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A visual analog scale is a pain assessment tool where individuals mark their pain level on a horizontal bar ranging from 0 to 10. The starting point of the scale indicates the absence of pain, while the end point indicates that the pain is unbearable. This table shows the woman's pain scale assessment. |
6 weeks
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Comparisons of Participants' Richard Campbell Sleep Scale (RCSQ) Scores Across and Within Groups
Tijdsspanne: 6 weeks
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The Richard Campbell Sleep Scale assesses the depth of sleep, the time it takes to fall asleep, the frequency of waking, the duration of wakefulness upon waking, the quality of sleep, and the noise level in the environment.
Each item on the scale is scored on a scale of 0 to 100.
A score of "0-25" indicates "very poor sleep," while a score of "76-100" indicates "very good sleep."
When calculating the total scale score, the scores from the 5 items are added together; the noise level in the environment is not included in the total score calculation.
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6 weeks
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Medewerkers en onderzoekers
Sponsor
Onderzoekers
- Studie directeur: Remzi KARASUNGUR, not affiliated
Studie record data
Bestudeer belangrijke data
Studie start (Werkelijk)
Primaire voltooiing (Werkelijk)
Studie voltooiing (Werkelijk)
Studieregistratiedata
Eerst ingediend
Eerst ingediend dat voldeed aan de QC-criteria
Eerst geplaatst (Werkelijk)
Updates van studierecords
Laatste update geplaatst (Werkelijk)
Laatste update ingediend die voldeed aan QC-criteria
Laatst geverifieerd
Meer informatie
Termen gerelateerd aan deze studie
Trefwoorden
Aanvullende relevante MeSH-voorwaarden
- Neurologische manifestaties
- Ziekten van het zenuwstelsel
- Psychische aandoening
- Pathologische processen
- Slaap-waakstoornissen
- Slaapstoornissen, intrinsiek
- Dyssomnieën
- Bekkenpijn
- Menstruatiestoornissen
- Pathologische aandoeningen, tekenen en symptomen
- Tekenen en symptomen
- Pijn
- Slaapinitiatie en -onderhoudsstoornissen
- Dysmenorroe
- Therapeutica
- Complementaire therapieën
- Patiëntenzorg
- Psychotherapie
- Gedragsdisciplines en activiteiten
- Revalidatie
- Nazorg
- Continuïteit van patiëntenzorg
- Zintuiglijke kunsttherapieën
- Muziektherapie
Andere studie-ID-nummers
- HKÜ-HEM-RK-01
Plan Individuele Deelnemersgegevens (IPD)
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Beschrijving IPD-plan
Informatie over medicijnen en apparaten, studiedocumenten
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