Relationships Among Physical and Psychological Status, Social Support, Resource Utilization, Supportive Care Needs in Patients With Gynecological Cancer

Sponsor
National Taiwan University Hospital (Other)
Overall Status
Enrolling by invitation
CT.gov ID
NCT05776693
Collaborator
(none)
200
1
13.2
15.1

Study Details

Study Description

Brief Summary

With the advancement of medical treatments and under the trend of prolonging the survival rate of gynecological cancer patients, the use of social resources and the need for supportive care are particularly important! In the past, studies on patients with gynecological cancer focused on the relation between physical and mental symptoms, intimate relationships, social support, and quality of life. There were few studies on the relationship between social support, resource utilization, and supportive care needs for this group of patients. Therefore, this study research will be conducted on these topics. The results of the study can confirm the current situation of gynecological cancer patients using social resources and the related factors that affect their supportive care needs, and can provide important empirical data for future social resource services and international research design content.

Condition or Disease Intervention/Treatment Phase

    Study Design

    Study Type:
    Observational
    Anticipated Enrollment :
    200 participants
    Observational Model:
    Cohort
    Time Perspective:
    Cross-Sectional
    Official Title:
    Relationships Among Physical and Psychological Status, Social Support, Resource Utilization, Supportive Care Needs in Patients With Gynecological Cancer
    Actual Study Start Date :
    Nov 24, 2022
    Anticipated Primary Completion Date :
    Jul 31, 2023
    Anticipated Study Completion Date :
    Dec 31, 2023

    Outcome Measures

    Primary Outcome Measures

    1. Supportive Care Needs Survey. [1 time points: From date of approaching patient until the date of first documented progression or date of death from any cause, whichever came first, assessed up to 100 months.]

      Patients' supportive care needs by Supportive Care Needs Survey.It is a 5-Point Likert Scale,higher scores mean more care needs.

    Secondary Outcome Measures

    1. Physical and Psychological Symptoms Scale [1 time points: From date of approaching patient until the date of first documented progression or date of death from any cause, whichever came first, assessed up to 100 months.]

      Patients' physical and psychological symptoms will be measured by Physical and Psychological Symptom Scale.It use Numerical Rating Scale(VRS)0-10.It is a 11 Point Likert Scale(e. g. 0 is no pain; 10 is unbearable pain) .

    2. Medical Outcomes Study Social Support Survey. [1 time points: From date of approaching patient until the date of first documented progression or date of death from any cause, whichever came first, assessed up to 100 months.]

      Patients' social support by Medical Outcomes Study Social Support Survey(MOS-SSS).It is a 5 Point Likert Scale(0-5) ,higher scores represents receiving more social support.

    3. Social resource assessment . [1 time points: From date of approaching patient until the date of first documented progression or date of death from any cause, whichever came first, assessed up to 100 months.]

      Patients' utilization of social resource assessment scale developed by the research team. It is a 5 Point Likert Scale(0-5).The higher the score, the more frequently the resource is used.Also answer how helpful and useful the resource is(0-10),higher scores represents more helpful and useful.

    Eligibility Criteria

    Criteria

    Ages Eligible for Study:
    20 Years to 100 Years
    Sexes Eligible for Study:
    Female
    Accepts Healthy Volunteers:
    No
    Inclusion Criteria:
    • Diagnosed by a physician as a patient with gynecological cancer

    • Aged 20 or above, with clear consciousness and able to communicate in Mandarin and Taiwanese.

    • After reading the consent form, accept the questionnaire.

    Exclusion Criteria:
    • Unconscious and unable to communicate verbally to complete the interview for this study

    Contacts and Locations

    Locations

    Site City State Country Postal Code
    1 National Taiwan University Taipei Taiwan 802

    Sponsors and Collaborators

    • National Taiwan University Hospital

    Investigators

    None specified.

    Study Documents (Full-Text)

    None provided.

    More Information

    Publications

    None provided.
    Responsible Party:
    National Taiwan University Hospital
    ClinicalTrials.gov Identifier:
    NCT05776693
    Other Study ID Numbers:
    • 202210084RINA
    First Posted:
    Mar 20, 2023
    Last Update Posted:
    Mar 20, 2023
    Last Verified:
    Dec 1, 2022
    Studies a U.S. FDA-regulated Drug Product:
    No
    Studies a U.S. FDA-regulated Device Product:
    No
    Keywords provided by National Taiwan University Hospital

    Study Results

    No Results Posted as of Mar 20, 2023