HOMECARE: SupporTive Care At Home Research for Patients With Advanced Cancer (STAHR-cancer)

Sponsor
Seoul National University Hospital (Other)
Overall Status
Recruiting
CT.gov ID
NCT05636384
Collaborator
Chung-Ang University Hosptial, Chung-Ang University College of Medicine (Other), DongGuk University (Other), Kyung Hee University Hospital (Other), Bundang CHA Hospital (Other), Seoul National University Bundang Hospital (Other)
396
6
2
53.2
66
1.2

Study Details

Study Description

Brief Summary

To test the effects of home-based care on unplanned hospitalization within 6 months among advanced cancer patients with decreased performance status. Home-based care includes education for patients and their family caregivers, home visits by specialized home-based medical staff, and regular status check-ups.

Condition or Disease Intervention/Treatment Phase
  • Other: Home-based care
N/A

Detailed Description

This study is a cluster, non-randomized controlled trial to test the effects of home-based care on unplanned hospitalization in 6 months among advanced cancer patients with decreased performance status. Home-based care includes education for patients and their family caregivers, home visits by specialized home-based medical staff, and regular status check-up. We are recruiting the study participants from 6 institutions, aiming for 396 cancer patients.

Participants for the intervention group will be recruited from Seoul National University Hospital, Chung-ang University Hospital, and Dongguk University Ilsan Hospital. Participants for the control group will be recruited from Kyung Hee University Medical Center, CHA Bundang Medical Center, and Seoul National University Bundang Hospital.

Study Design

Study Type:
Interventional
Anticipated Enrollment :
396 participants
Allocation:
Non-Randomized
Intervention Model:
Parallel Assignment
Intervention Model Description:
A cluster, non-randomized controlled trialA cluster, non-randomized controlled trial
Masking:
None (Open Label)
Primary Purpose:
Supportive Care
Official Title:
SupporTive Care At Home Research (STAHR): a Cluster Non-randomized Controlled Trial for Patients With Advanced Cancer
Actual Study Start Date :
Jul 25, 2022
Anticipated Primary Completion Date :
Dec 31, 2026
Anticipated Study Completion Date :
Dec 31, 2026

Arms and Interventions

Arm Intervention/Treatment
Experimental: Intervention

Patients enrolled in the intervention cluster (institution) are given specialized home-based medical care based on a specialized home-based medical team approach.

Other: Home-based care
Home-based medical care is based on a specialized home-based medical team approach, including following: Specialized Home-Based Medical Team Approach Initial Assessment and Education Initial Home Visits and Education Multidisciplinary Team Meeting Regular Assessment After the Initial Visit

No Intervention: Control

Patients enrolled in the control cluster (institution) are only given the educational materials. Except for the home-based care intervention, usual care for advanced cancer patients was not restricted for these patients.

Outcome Measures

Primary Outcome Measures

  1. Unplanned hospitalization [within 6 months following enrollment]

    admission to the enrolled hospital to treat unexpected symptoms or medical conditions (not including planned admission for chemotherapy or admission for planned surgery or intervention) admission to a hospital other than the enrolled hospital admission to a nursing hospital for a duration of less than 4 weeks.

Secondary Outcome Measures

  1. Patient medical utilization [within 6 months following enrollment]

    The total number of hospital utilization, including hospitalization, emergency room visit, and clinic visits

  2. Hospitalization [within 6 months following enrollment]

    the number of hospitalization

  3. ER visits [within 6 months following enrollment]

    the number of emergency room visits

  4. Healthcare use [within 6 months following enrollment]

    the number of healthcare use for severe diseases

  5. Patient end-of-life care: ICU admission [within 1 month before death]

    ICU admission one month before death

  6. Patient end-of-life care: ventilator treatment [within 1 month before death]

    Mechanical ventilator apply one month before death

  7. Patient end-of-life care: an advance directive [within 1 month before death]

    Completion of advance medical directives within 1 month before death

  8. Quality of life of patient - ESAS [within 6 months following enrollment]

    Modified Edmonton Symptom Assessment System (ESAS) of patient

  9. Quality of life of patient - EQ-5D [within 6 months following enrollment]

    Euro-Quality of Life-5 Dimension (EQ-5D) of patient

  10. Depressive symptom of patient [within 6 months following enrollment]

    Patient Health Questionnaire-9 (PHQ-9) of patient

  11. Satisfaction with services (patient) [within 6 months following enrollment]

    Satisfaction of the study participant (patient) with the service in this study, evaluated by questionnaire

  12. Quality of life of family caregiver [within 6 months following enrollment]

    Euro-Quality of Life-5 Dimension (EQ-5D) of family caregiver

  13. Care burden of family caregiver [within 6 months following enrollment]

    The Korean version of Caregiver Reaction Assessment (CRA-K) of family caregiver

  14. Depressive symptom of family caregiver [within 6 months following enrollment]

    Patient Health Questionnaire-9 (PHQ-9) of family caregiver

  15. Caring competency of family caregiver [within 6 months following enrollment]

    Caring competency of family caregiver, measured by questionnaire

  16. Satisfaction with services (family caregiver) [within 6 months following enrollment]

    Satisfaction of the study participant (family caregiver) with the service in this study, evaluated by questionnaire

  17. Expenses [within 6 months following enrollment]

    medical expenses, care expenses

Eligibility Criteria

Criteria

Ages Eligible for Study:
19 Years and Older
Sexes Eligible for Study:
All
Accepts Healthy Volunteers:
No
Inclusion Criteria:

Both the patient and their family caregiver must meet the criteria to be considered for this research.

  1. Patient

  2. A person who has an advanced-stage solid cancer diagnosis (ICD-10 code C00-C70); A person who is receiving or planning to receive cancer treatment

  3. A person who meets one of the following conditions

  4. Has been evaluated as having ECOG performance status 2

  5. Has been evaluated as having ECOG performance status 1 and is over 70 years of age

  6. A person who wishes to stay at home

  7. A person whose family caregiver resides at home

  8. A person who wishes to participate in the research

  9. Family Caregiver

  10. A family* member of the patient

  • Family: refers to the patient's spouse (including a common-law partner), descendants and their spouses up to the second degree, siblings and their spouses, and relatives and their spouses up to the eighth degree.
  1. A person who meets one of the following conditions:

  2. Lives with the patient (patient's household member)

  3. Does not live with the patient, but visits the patient's home more than three times a week

  4. A person who wants the patient to stay at home

  5. A person who can communicate easily with medical staff

  6. A person who wishes to participate in the research

Exclusion Criteria:

If either the patient or the family caregiver meets any one of these criteria, they are excluded from the study.

  1. Patient

  2. A person who cannot speak, hear, or read Korean

  3. A person who is judged by a medical doctor to be unable to take part in this research due to extremely poor health

  4. A person residing outside the range that can be visited by the respective medical institution (the conditions for distance are to be specified by each medical institution)*

  • This condition is not applicable for the control group.
  1. A person who has used hospital- or home-type hospice and palliative care services

  2. A person who is under the age of 19

  3. Family Caregiver

  4. A person who cannot speak, hear, or read Korean

  5. A person who is judged by a medical doctor to be unable to take part in this research due to extremely poor health

  6. A person under the age of 19

Contacts and Locations

Locations

Site City State Country Postal Code
1 Dongguk University Medical Center Goyang-si Gyeonggi-do Korea, Republic of
2 Bundang CHA Hospital Seongnam-si Gyeonggi-do Korea, Republic of
3 Seoul National University Bundang Hospital Seongnam-si Gyeonggi-do Korea, Republic of
4 Seoul National University Hospital Seoul Korea, Republic of 03080
5 Chung-Ang University Hosptial Seoul Korea, Republic of
6 Kyung Hee University Hospital Seoul Korea, Republic of

Sponsors and Collaborators

  • Seoul National University Hospital
  • Chung-Ang University Hosptial, Chung-Ang University College of Medicine
  • DongGuk University
  • Kyung Hee University Hospital
  • Bundang CHA Hospital
  • Seoul National University Bundang Hospital

Investigators

  • Principal Investigator: Belong Cho, MD, MPH, PhD, Seoul National University Hospital

Study Documents (Full-Text)

None provided.

More Information

Publications

None provided.
Responsible Party:
BeLong Cho, Professor, Seoul National University Hospital
ClinicalTrials.gov Identifier:
NCT05636384
Other Study ID Numbers:
  • HC21C0115-1
First Posted:
Dec 5, 2022
Last Update Posted:
Dec 5, 2022
Last Verified:
Nov 1, 2022
Individual Participant Data (IPD) Sharing Statement:
No
Plan to Share IPD:
No
Studies a U.S. FDA-regulated Drug Product:
No
Studies a U.S. FDA-regulated Device Product:
No
Additional relevant MeSH terms:

Study Results

No Results Posted as of Dec 5, 2022