- ICH GCP
- US Clinical Trials Registry
- Klinisk forsøg NCT05576545
Udvikle og evaluere effektiviteten af en selvpleje-smartphone-applikation med hensyn til selveffektivitet og modstandsdygtighed blandt nydiagnosticerede brystkræftpatienter, der gennemgår behandling
10. oktober 2022 opdateret af: Hsin-Tien Hsu, Kaohsiung Medical University Chung-Ho Memorial Hospital
Denne undersøgelse skulle udvikle og evaluere selveffektiviteten og modstandsdygtigheden af Breast Cancer Self-Care-appen hos nydiagnosticerede brystkræftpatienter, der gennemgår kemoterapi.
Studieoversigt
Status
Afsluttet
Intervention / Behandling
Detaljeret beskrivelse
Denne undersøgelse skulle udvikle og evaluere selveffektiviteten og modstandsdygtigheden af Breast Cancer Self-Care-appen hos nydiagnosticerede brystkræftpatienter, der gennemgår kemoterapi.
I den første fase af denne undersøgelse, udvikle en prototype af Breast Cancer Self-Care App ved at udføre patientinterviews.
I den anden fase, et eksperimentelt to-gruppe pretest-posttest kvantitativt studiedesign til at evaluere selveffektiviteten og modstandsdygtigheden af Breast Cancer Self-Care-appen hos nydiagnosticerede brystkræftpatienter, der gennemgår kemoterapi.
Patienterne blev randomiseret til forsøgs- og kontrolgrupperne.
Patienterne i kontrolgruppen modtog generel rutinepleje, og patienterne i forsøgsgruppen modtog generel rutinepleje plus interventionen i Breast Cancer Self-Care App.
Begge grupper udfyldte et grundlæggende spørgeskemaer om demografi, selveffektivitet og modstandsdygtighed ved prætesten og efter fire uger.
Undersøgelsestype
Interventionel
Tilmelding (Faktiske)
73
Fase
- Ikke anvendelig
Kontakter og lokationer
Dette afsnit indeholder kontaktoplysninger for dem, der udfører undersøgelsen, og oplysninger om, hvor denne undersøgelse udføres.
Studiesteder
-
-
-
Kaohsiung, Taiwan, 807
- Kaohsiung Medical University
-
-
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
20 år til 65 år (VOKSEN, OLDER_ADULT)
Tager imod sunde frivillige
Ingen
Køn, der er berettiget til at studere
Alle
Beskrivelse
Inklusionskriterier:
- Klar bevidsthed, over 20 år gammel, kan kommunikere på mandarin og taiwanesisk
- Diagnosticeret brystkræft I-III stadium
- gennemgå den første kemoterapi
- Hav en smartphone
- Modtager behandling: EC/EC+T/LC/LC+T E: (Epirubicin)、C: (Cyclophosphamid)、L: (Lipo-Dox)、T: (Taxotere)
Ekskluderingskriterier:
- DSM-V psykisk syg
- IOS system smartphone
- over 65 år
Studieplan
Dette afsnit indeholder detaljer om studieplanen, herunder hvordan undersøgelsen er designet, og hvad undersøgelsen måler.
Hvordan er undersøgelsen tilrettelagt?
Design detaljer
- Primært formål: ANDET
- Tildeling: TILFÆLDIGT
- Interventionel model: PARALLEL
- Maskning: ENKELT
Våben og indgreb
Deltagergruppe / Arm |
Intervention / Behandling |
|---|---|
|
EKSPERIMENTEL: generel rutinepleje og Breast Cancer Self-Care-appen
|
Breast Cancer Self-Care-appen indeholder flere dele - introduktion til brystkræft, behandlingstyper, pleje af bivirkninger, ernæring, afslapningsvideoer, forsikring, medicinske nyheder og registrering af bivirkninger osv.
Forskeren hjalp med at installere appen på patientens mobiltelefon, indtastede den personlige konto og bad patienten om at udfylde spørgeskemaer.
Patienterne fik individuel sundhedsuddannelsesopgave i Breast Cancer Self-Care-appen hver uge afhængigt af typen af kemoterapi.
Efter fire uger udfyldte de spørgeskemaer igen.
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NO_INTERVENTION: almindelig rutinepleje
|
Hvad måler undersøgelsen?
Primære resultatmål
Resultatmål |
Foranstaltningsbeskrivelse |
Tidsramme |
|---|---|---|
|
Self-efficacy
Tidsramme: 4 uger
|
Use Strategies Used by People to Promote Health (SUPPH) måler egenomsorgseffektivitet.
Skalaen i alt på 29 punkter måler egenomsorgs-self-efficacy.
Der er 3 underskalaer for hver af følgende: Stressreduktion (10 punkter, 5-50 point), at træffe beslutninger (3 punkter, 3-15 point), positiv holdning (16 punkter, 16-80 point).
Skalaens samlede score er 29-145.
Den viser, at egenomsorgs-self-efficacy stiger, når de samlede punkter på skalaen stiger.
|
4 uger
|
Sekundære resultatmål
Resultatmål |
Foranstaltningsbeskrivelse |
Tidsramme |
|---|---|---|
|
Modstandsdygtighed
Tidsramme: 4 uger
|
Brug Resilience skala 14 elementer (RS-14) måler individuel modstandskraft.
Skalaen med i alt 14 punkter måler modstandskraft.
Skalaens samlede score er 14-98.
Det viser, at modstandskraften øges, når de samlede punkter på skalaen stiger.
|
4 uger
|
Samarbejdspartnere og efterforskere
Det er her, du vil finde personer og organisationer, der er involveret i denne undersøgelse.
Publikationer og nyttige links
Den person, der er ansvarlig for at indtaste oplysninger om undersøgelsen, leverer frivilligt disse publikationer. Disse kan handle om alt relateret til undersøgelsen.
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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)
18. september 2020
Primær færdiggørelse (FAKTISKE)
15. august 2022
Studieafslutning (FAKTISKE)
15. august 2022
Datoer for studieregistrering
Først indsendt
26. september 2022
Først indsendt, der opfyldte QC-kriterier
10. oktober 2022
Først opslået (FAKTISKE)
12. oktober 2022
Opdateringer af undersøgelsesjournaler
Sidste opdatering sendt (FAKTISKE)
12. oktober 2022
Sidste opdatering indsendt, der opfyldte kvalitetskontrolkriterier
10. oktober 2022
Sidst verificeret
1. oktober 2022
Mere information
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Yderligere relevante MeSH-vilkår
Andre undersøgelses-id-numre
- KMUHIRB-E(I)-20200041
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