- ICH GCP
- US Clinical Trials Registry
- Klinisk forsøg NCT04356820
The Effect of Music Played and Acupressure Application on Pain and Anxiety in Women Undergoing Gynecological Examination
20. april 2020 opdateret af: Didem Kucukkelepce, Adiyaman University Research Hospital
This study was carried out to determine the effect of listening to music and acupressure application in reducing pain and anxiety during gynecological examination.
Studieoversigt
Undersøgelsestype
Interventionel
Tilmelding (Faktiske)
156
Fase
- Ikke anvendelig
Kontakter og lokationer
Dette afsnit indeholder kontaktoplysninger for dem, der udfører undersøgelsen, og oplysninger om, hvor denne undersøgelse udføres.
Studiesteder
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Adıyaman, Kalkun, 02100
- Didem Şimşek Küçükkelepçe
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Deltagelseskriterier
Forskere leder efter personer, der passer til en bestemt beskrivelse, kaldet berettigelseskriterier. Nogle eksempler på disse kriterier er en persons generelle helbredstilstand eller tidligere behandlinger.
Berettigelseskriterier
Aldre berettiget til at studere
19 år til 65 år (Voksen, Ældre voksen)
Tager imod sunde frivillige
Ingen
Køn, der er berettiget til at studere
Kvinde
Beskrivelse
Inclusion Criteria:
- - not to be pregnant,
- no hearing problems
- Being between the ages of 19 and 65, Not having any psychiatric illness,
- No gynecological cancer, Not to have any deformity in her extremities
Exclusion Criteria:
-
Studieplan
Dette afsnit indeholder detaljer om studieplanen, herunder hvordan undersøgelsen er designet, og hvad undersøgelsen måler.
Hvordan er undersøgelsen tilrettelagt?
Design detaljer
- Primært formål: Støttende pleje
- Tildeling: Randomiseret
- Interventionel model: Faktoriel opgave
- Maskning: Enkelt
Våben og indgreb
Deltagergruppe / Arm |
Intervention / Behandling |
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Ingen indgriben: styring
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Eksperimentel: acupressure
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Data collection took about 10 to 15 minutes.
Then the woman invited to the examination room was asked to pull one of the envelopes with the names of the groups.
The women who pulled the acupressure envelope were given a semi-sitting position where the acupressure application can feel comfortable and the researcher can easily apply the acupressure points.
Before the acupressure application, massage was applied for 30 seconds to ensure circulation.
Afterwards, 90 seconds consecutive pressures were applied to the specified acupressure points in a certain order (SP 6, Li 4), taking into account the direction of the meridian.
After the examination, the pain formed during the gynecological examination was evaluated by applying the Short Form-McGill Pain Questionnaire without leaving the examination room
Andre navne:
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Eksperimentel: music
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Data collection took about 10 to 15 minutes.
Then the woman invited to the examination room was asked to pull one of the envelopes with the names of the groups.
The women who pulled the acupressure envelope were given a semi-sitting position where the acupressure application can feel comfortable and the researcher can easily apply the acupressure points.
Before the acupressure application, massage was applied for 30 seconds to ensure circulation.
Afterwards, 90 seconds consecutive pressures were applied to the specified acupressure points in a certain order (SP 6, Li 4), taking into account the direction of the meridian.
After the examination, the pain formed during the gynecological examination was evaluated by applying the Short Form-McGill Pain Questionnaire without leaving the examination room
Andre navne:
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Hvad måler undersøgelsen?
Primære resultatmål
Resultatmål |
Foranstaltningsbeskrivelse |
Tidsramme |
---|---|---|
questionnaire and scale
Tidsramme: 12 weeks
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McGill pain scale was developed by Melzack in 1987 and its validity and reliability in Turkish Yakut et al. (2007).
In this study, the Short Form-McGill Pain Questionnaire (KF-MAA), whose validity and reliability was used and frequently used by Biçici (2010), was applied.
This questionnaire consists of a total of 15 descriptive words to determine the sensory (11 words) and affective (4 words) dimensions of pain.
In this section, the severity of pain (0 = none, 1 = mild, 2 = moderate, 3 = severe) is evaluated and three pain scores (sensory, affective and total pain rate = sensory affective) are obtained.
In addition, the pain felt at the time of measurement is measured with the Visuel Analog Scale (VAS) and the total pain intensity is measured with a 6-point Likert scale.
On this scale, 0 = no pain, 1 = mild, 2 = disturbing, 3 = distressing, 4 = terrible, 5 = unbearable pain.
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12 weeks
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Samarbejdspartnere og efterforskere
Det er her, du vil finde personer og organisationer, der er involveret i denne undersøgelse.
Datoer for undersøgelser
Disse datoer sporer fremskridtene for indsendelser af undersøgelsesrekord og resumeresultater til ClinicalTrials.gov. Studieregistreringer og rapporterede resultater gennemgås af National Library of Medicine (NLM) for at sikre, at de opfylder specifikke kvalitetskontrolstandarder, før de offentliggøres på den offentlige hjemmeside.
Studer store datoer
Studiestart (Faktiske)
1. maj 2019
Primær færdiggørelse (Faktiske)
15. juli 2019
Studieafslutning (Faktiske)
10. september 2019
Datoer for studieregistrering
Først indsendt
16. april 2020
Først indsendt, der opfyldte QC-kriterier
20. april 2020
Først opslået (Faktiske)
22. april 2020
Opdateringer af undersøgelsesjournaler
Sidste opdatering sendt (Faktiske)
22. april 2020
Sidste opdatering indsendt, der opfyldte kvalitetskontrolkriterier
20. april 2020
Sidst verificeret
1. april 2020
Mere information
Begreber relateret til denne undersøgelse
Nøgleord
Yderligere relevante MeSH-vilkår
Andre undersøgelses-id-numre
- Adıyaman_Universty
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