Effekten av Ho'Oponopono-teknikken på stomitilpasning, kroppsbilde og livskvalitet
Effekten av Ho'Oponopono-teknikken på tilpasning til stomi, kroppsbilde og livskvalitet hos pasienter med kolostomi: En randomisert kontrollert studie
Studieoversikt
Status
Forhold
Intervensjon / Behandling
Studietype
Registrering (Faktiske)
Fase
- Ikke aktuelt
Kontakter og plasseringer
Studiesteder
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Istanbul, Tyrkia (Türkiye)
- Istanbul Basaksehir Cam and Sakura City Hospital
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Deltakelseskriterier
Kvalifikasjonskriterier
Alder som er kvalifisert for studier
- Voksen
- Eldre voksen
Tar imot friske frivillige
Beskrivelse
Inklusjonskriterier:
Planlagt for kolostomi
18 år eller eldre
Kan snakke og forstå tyrkisk
Lesekyndig (kan lese og skrive)
Villig til å delta i studien
Eksklusjonskriterier:
Har kommunikasjonsproblemer
Har en nevrologisk eller psykiatrisk lidelse
Studieplan
Hvordan er studiet utformet?
Designdetaljer
- Primært formål: Støttende omsorg
- Tildeling: Randomisert
- Intervensjonsmodell: Parallell tildeling
- Masking: Ingen (Open Label)
Våpen og intervensjoner
Deltakergruppe / Arm |
Intervensjon / Behandling |
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Eksperimentell: Ho'oponopono-teknikken intervensjon
Ho'oponopono-teknikken vil bli anvendt på pasienter i intervensjonsgruppen etter operasjon.
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The Ho'oponopono technique will be applied on postoperative days 1, 2, and 3 at 10:00 a.m. and will continue until the end of the first month.
Data will be collected using the study scales on days 1, 3, and 10, and at the end of the first month.
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Aktiv komparator: Kontrollgruppe (standard behandling)
Ingen intervensjon vil bli utført for pasientene i denne gruppen.
Skalaene som skal brukes i studien vil bli administrert innenfor samme tidsramme som i intervensjonsgruppen.
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Standard behandling gis til personer som har fått et stomi laget i postoperativ perioden.
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Hva måler studien?
Primære resultatmål
Resultatmål |
Tiltaksbeskrivelse |
Tidsramme |
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Quality of Life as Assessed by the Stoma Quality of Life Scale (Stoma-QOL) Total Score
Tidsramme: The Ho'oponopono technique will be applied on postoperative days 1, 2, and 3 at 10:00 a.m. and will continue until the end of the first month. Data will be collected using the study scales on days 1, 3, and 10, and at the end of the first month.
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Quality of life in individuals with an ostomy will be evaluated using the Baxter et al. Stoma Quality of Life Scale (Stoma-QOL), a standardized self-report questionnaire specifically developed for individuals with a stoma. The scale consists of 21 items that measure stoma-related quality of life. The first two items assess overall life satisfaction and are scored from 0 to 100, with higher scores indicating greater satisfaction. The remaining items evaluate three subdimensions: work and social life (6 items), sexuality and body image (5 items), and stoma function (6 items), and one item assesses perceived economic status. Item scores are summed and transformed according to the scoring manual to obtain a total score. The total Stoma-QOL score will be used as the single reported outcome, with higher scores indicating better quality of life. Score range: 0-100 Minimum: 0 Maximum: 100 Higher scores indicate better quality of life. |
The Ho'oponopono technique will be applied on postoperative days 1, 2, and 3 at 10:00 a.m. and will continue until the end of the first month. Data will be collected using the study scales on days 1, 3, and 10, and at the end of the first month.
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Ostomy Adjustment Level as Assessed by the Ostomy Adjustment Scale (OAS) Total Score
Tidsramme: The Ho'oponopono technique will be applied on postoperative days 1, 2, and 3 at 10:00 a.m. and will continue until the end of the first month. Data will be collected using the study scales on days 1, 3, and 10, and at the end of the first month.
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Adaptation to living with an ostomy will be evaluated using the Ostomy Adjustment Scale, a Likert-type, self-report measurement tool that provides a quantitative assessment of overall ostomy adjustment. The scale includes items addressing physical adjustment (stoma care, pouch management, and ability to perform daily activities), psychological adjustment (acceptance of the ostomy, anxiety, body image, and self-esteem), social adjustment (participation in social relationships, comfort in social environments, and perceived stigma), and coping and adaptation skills (problem-solving, use of support resources, and managing daily life with an ostomy). Each item is scored on a Likert scale, and item scores are summed to obtain a total score. The total score will be used as the single reported outcome, with higher scores indicating better adjustment to the ostomy. Score range: 34-204 Minimum: 34 Maximum: 204 Higher scores indicate better adjustment to the ostomy. |
The Ho'oponopono technique will be applied on postoperative days 1, 2, and 3 at 10:00 a.m. and will continue until the end of the first month. Data will be collected using the study scales on days 1, 3, and 10, and at the end of the first month.
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Body Image Perception as Assessed by the Body Image Scale (BIS) Total Score
Tidsramme: The Ho'oponopono technique will be applied on postoperative days 1, 2, and 3 at 10:00 a.m. and will continue until the end of the first month. Data will be collected using the study scales on days 1, 3, and 10, and at the end of the first month.
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Body image perception in individuals with an ostomy will be evaluated using the Body Image Scale, a self-report psychometric instrument that quantitatively measures satisfaction with body appearance and attitudes toward the body. The scale consists of Likert-type items assessing affective, cognitive, and behavioral responses related to body image. Each item is scored on a 4-point scale, and the item scores are summed to obtain a total score. The total score will be used as the single reported outcome. Higher scores indicate greater body image disturbance, whereas lower scores reflect a more positive body image perception. Score range: 0-30 Minimum: 0 Maximum: 30 Higher scores indicate poorer body image. |
The Ho'oponopono technique will be applied on postoperative days 1, 2, and 3 at 10:00 a.m. and will continue until the end of the first month. Data will be collected using the study scales on days 1, 3, and 10, and at the end of the first month.
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Samarbeidspartnere og etterforskere
Sponsor
Studierekorddatoer
Studer hoveddatoer
Studiestart (Faktiske)
Primær fullføring (Faktiske)
Studiet fullført (Faktiske)
Datoer for studieregistrering
Først innsendt
Først innsendt som oppfylte QC-kriteriene
Først lagt ut (Faktiske)
Oppdateringer av studieposter
Sist oppdatering lagt ut (Faktiske)
Siste oppdatering sendt inn som oppfylte QC-kriteriene
Sist bekreftet
Mer informasjon
Begreper knyttet til denne studien
Andre studie-ID-numre
- Ho'oponopono Technique
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