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Sense of Hope Alleviates Fatigue in Breast Cancer Survivors

22. marts 2015 opdateret af: National Taiwan University Hospital

The Sense of Hope Alleviates Fatigue in Breast Cancer Survivors

This study explores the relationship between the sense of hope and fatigue in breast cancer survivors and provides a reference for future planning improvements for breast cancer survivors experiencing fatigue.

Studieoversigt

Status

Ukendt

Betingelser

Detaljeret beskrivelse

Breast cancer is an important and escalating issue for females all over the world. Due to the improvement of medical and technological progress, the survival rate of breast cancer patient increases every year. Breast cancer survivors, after the discomforting distress from cancer treatment, will go through treatment-derived physical distress and worry about relapse. As a result the fatigue in breast cancer survivors has not been reduced after primary treatment. Feeling fatigue in a long term will bring mental illness problems ,decrease the quality of life and weaken the will to survive. A sense of hope in the face of fatigue may serve as an important driving force and enhance the survivors' will to survive. This study explores the relationship between the sense of hope and fatigue in breast cancer survivors and provides a reference for future planning improvements for breast cancer survivors experiencing fatigue.

A cross-sectional study design is adopted for this study. The study expects to collect 200 questionnaires from breast cancer survivors through medical centers treating breast cancer and breast cancer patients communities. The questionnaire includes (a) the basic demographic information (b) disease history (c) social support scale; (d) short version multiaxial fatigue syndrome scale; (e) Hearst hope scale.

Answered questionnaires will be input to spreadsheets for further statistical analysis using SPSS 19.0 statistical software packages.

Undersøgelsestype

Observationel

Tilmelding (Forventet)

180

Kontakter og lokationer

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

Studiesteder

  • Taiwan
      • Taipei, Taiwan, 10002
        • Rekruttering
        • National Taiwan University Hospital
        • 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

20 år til 90 år (Voksen, Ældre voksen)

Tager imod sunde frivillige

Ingen

Køn, der er berettiget til at studere

Kvinde

Prøveudtagningsmetode

Ikke-sandsynlighedsprøve

Studiebefolkning

breast cancer survivors,complete chemotherapy and radiotherapy

Beskrivelse

Inclusion criteria:

  1. diagnosed as a breast cancer patient
  2. complete operation,chemotherapy and radiation therapy
  3. understand the treatment and condition by herself
  4. conscious clear who can speaking Mandarin or: Taiwanese
  5. after consenting , the participant agree to participate orally or write down in the consent form

Exclusion criteria:

  1. Can not speaking Mandarin or Taiwanese
  2. Psychotic or Understanding barriers
  3. refuse verbally or write the Consent Form

Studieplan

Dette afsnit indeholder detaljer om studieplanen, herunder hvordan undersøgelsen er designet, og hvad undersøgelsen måler.

Hvordan er undersøgelsen tilrettelagt?

Design detaljer

  • Tidsperspektiver: Tværsnit

Kohorter og interventioner

Gruppe / kohorte
Breast cancer survivor
Females finished primary breast cancer treatment including surgical operation, radiation therapy and chemotherapy.

Hvad måler undersøgelsen?

Primære resultatmål

Resultatmål
Foranstaltningsbeskrivelse
Tidsramme
Multidimensional Fatigue Symptom Inventory-Short Form
Tidsramme: Baseline measured after the completion of breast cancer surgery, radiation therapy and chemotherapy
A 30-item self-report questionnaire designed to assess the severity, frequency, and daily pattern of fatigue as well as its perceived interference with quality of life.
Baseline measured after the completion of breast cancer surgery, radiation therapy and chemotherapy

Sekundære resultatmål

Resultatmål
Foranstaltningsbeskrivelse
Tidsramme
Herth Hope Index
Tidsramme: Baseline measured after the completion of breast cancer surgery, radiation therapy and chemotherapy
A 12-item self-report questionnaire containing three dimensions: temporality and future, positive readiness and expectancy, and interconnectedness. Tested on family caregivers of terminally ill people and terminally ill persons as well as in community and hospital patients and family members. (Herth, 1990)
Baseline measured after the completion of breast cancer surgery, radiation therapy and chemotherapy
The Inventory of Socially Supportive Behaviors
Tidsramme: Baseline measured after the completion of breast cancer surgery, radiation therapy and chemotherapy
A 40-item self-report questionnaire designed to assess how often individuals received various forms of assistance during the preceding month, such as directive guidance (e.g., offering advice), nondirective support (e.g., listening and reflecting), positive social exchange (e.g., expressing confidence and encouragement), and tangible assistance (e.g., providing materials or services). (Barrera, Sandler, & Ramsay, 1981).
Baseline measured after the completion of breast cancer surgery, radiation therapy and chemotherapy

Samarbejdspartnere og efterforskere

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

Sponsor

National Taiwan University Hospital

Efterforskere

  • Ledende efterforsker: ChunaNG Pei-Hsuan, National Taiwan University Hospital

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.

Generelle publikationer

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

1. januar 2015

Primær færdiggørelse (Forventet)

1. juli 2015

Studieafslutning (Forventet)

1. juli 2015

Datoer for studieregistrering

Først indsendt

6. januar 2015

Først indsendt, der opfyldte QC-kriterier

18. marts 2015

Først opslået (Skøn)

19. marts 2015

Opdateringer af undersøgelsesjournaler

Sidste opdatering sendt (Skøn)

24. marts 2015

Sidste opdatering indsendt, der opfyldte kvalitetskontrolkriterier

22. marts 2015

Sidst verificeret

1. marts 2015

Mere information

Begreber relateret til denne undersøgelse

Nøgleord

Yderligere relevante MeSH-vilkår

Andre undersøgelses-id-numre

  • 201411051RINB

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 .

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