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Health Behavior Intervention for Colorectal Cancer Patients

2. juni 2026 opdateret af: Xiaoxiao Hu, Nanjing Medical University

A Study on Health Behavior Intervention for Colorectal Cancer Patients Based on the Theory of Time-bound Self-regulation

Develop a health behavior intervention plan based on patients' needs and preferences, and preliminarily apply and evaluate the feasibility and effectiveness of this intervention plan for patients with colorectal cancer.

Studieoversigt

Status

Ikke rekrutterer endnu

Betingelser

Intervention / Behandling

Undersøgelsestype

Interventionel

Tilmelding (Anslået)

40

Fase

  • Ikke anvendelig

Kontakter og lokationer

Dette afsnit indeholder kontaktoplysninger for dem, der udfører undersøgelsen, og oplysninger om, hvor denne undersøgelse udføres.

Studiekontakt

Studiesteder

  • Kina
    • Jiangsu
      • Nanjing, Jiangsu, Kina
        • 101 Longmian Avenue, Jiangning District
        • Kontakt:

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

  • Voksen
  • Ældre voksen

Tager imod sunde frivillige

Ingen

Beskrivelse

Inclusion Criteria:

Age ≥ 18 years; patients who meet the diagnostic criteria for colorectal cancer outlined in the "Chinese Guidelines for the Diagnosis and Treatment of Colorectal Cancer (2023 Edition)" and for whom the time since surgery is ≥ 3 months; patients who are able to understand the study and complete the questionnaire independently; and patients who voluntarily agree to participate.

Exclusion Criteria:

Patients with severe cardiac, hepatic, or renal insufficiency or other serious systemic diseases; patients with cognitive or psychiatric disorders; patients with severe postoperative complications (such as anastomotic leakage or severe wound infection); patients with metastatic cancer or concurrent malignant tumors; patients with a life expectancy of less than 6 months.

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: Ikke-randomiseret
  • Interventionel model: Sekventiel tildeling
  • Maskning: Enkelt

Våben og indgreb

Deltagergruppe / Arm
Intervention / Behandling
Eksperimentel: intervention group
Based on providing routine post-operative health education services for colorectal cancer patients in the hospital, additional health behavior intervention programs based on the theory of time-limited self-regulation are also received.
Adfærdsmæssigt: health behavior intervention programs based on the temporal self-regulation theory are also received
The intervention group received additional health behavior intervention programs based on the temporal self-regulation theory in addition to the routine post-operative health education services provided by the hospital. The intervention period was set as 1 session per week for a total of 6 weeks, each session lasting approximately 45-60 minutes. The intervention was conducted in a combination of offline and online guidance and support. Before the intervention, baseline assessments were conducted for the research subjects, and intervention manuals, demonstration videos, and other tools were distributed. From the 1st to the 5th week, corresponding module measures were implemented according to the intervention framework, including looking to the future, intention strengthening, habit shaping, and self-control. In the 6th week, progress summaries, feedback, and long-term plan formulation were carried out. Throughout the process, online WeChat/QQ support groups/Tencent Meeting were u
Ingen indgriben: control group
Regular post-operative health education services for colorectal cancer

Hvad måler undersøgelsen?

Primære resultatmål

Resultatmål
Foranstaltningsbeskrivelse
Tidsramme
health behavior
Tidsramme: From before the intervention (T0) to 3 months after the intervention (T2)
Measured through the Health Behavior Scale for Cancer Patient
From before the intervention (T0) to 3 months after the intervention (T2)

Sekundære resultatmål

Resultatmål
Foranstaltningsbeskrivelse
Tidsramme
Health behavior intention
Tidsramme: From before the intervention (T0) to three months after the intervention (T2)
Measured through the Health Behavior Intention Scale
From before the intervention (T0) to three months after the intervention (T2)
Future Time Perspective
Tidsramme: From before the intervention (T0) to three months after the intervention (T2)
Measured through the Consideration of Future Consequences Scale
From before the intervention (T0) to three months after the intervention (T2)
Behavioral prepotency
Tidsramme: From before the intervention (T0) to three months after the intervention (T2)
Measured through the Self-Reported Behavioral Automaticity Index
From before the intervention (T0) to three months after the intervention (T2)

Samarbejdspartnere og efterforskere

Det er her, du vil finde personer og organisationer, der er involveret i denne undersøgelse.

Sponsor

Nanjing Medical University

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 (Anslået)

15. juni 2026

Primær færdiggørelse (Anslået)

30. december 2026

Studieafslutning (Anslået)

30. januar 2027

Datoer for studieregistrering

Først indsendt

2. juni 2026

Først indsendt, der opfyldte QC-kriterier

2. juni 2026

Først opslået (Faktiske)

8. juni 2026

Opdateringer af undersøgelsesjournaler

Sidste opdatering sendt (Faktiske)

8. juni 2026

Sidste opdatering indsendt, der opfyldte kvalitetskontrolkriterier

2. juni 2026

Sidst verificeret

1. juni 2026

Mere information

Begreber relateret til denne undersøgelse

Nøgleord

Yderligere relevante MeSH-vilkår

Andre undersøgelses-id-numre

  • 2025-SR-1017

Plan for individuelle deltagerdata (IPD)

Planlægger du at dele individuelle deltagerdata (IPD)?

INGEN

IPD-planbeskrivelse

IPD sharing is not allowed due to ethical and consent-related restrictions.

Lægemiddel- og udstyrsoplysninger, undersøgelsesdokumenter

Studerer et amerikansk FDA-reguleret lægemiddelprodukt

Ingen

Studerer et amerikansk FDA-reguleret enhedsprodukt

Ingen

Disse oplysninger blev hentet direkte fra webstedet clinicaltrials.gov uden ændringer. Hvis du har nogen anmodninger om at ændre, fjerne eller opdatere dine undersøgelsesoplysninger, bedes du kontakte register@clinicaltrials.gov. Så snart en ændring er implementeret på clinicaltrials.gov, vil denne også blive opdateret automatisk på vores hjemmeside .

Kliniske forsøg med Kolorektal cancer

Søg i lignende forsøg

Sponsorer og samarbejdspartnere

Medicinske tilstande

Narkotikainterventioner

CROs by country

CROs in Albania

Betingelser

Sjældne sygdomme

Narkotikainterventioner

Kosttilskud

Sponsor / samarbejdspartnere

Placeringer

Abonner