- ICH GCP
- US Clinical Trials Registry
- Clinical Trial NCT02483390
Use of Online Communications to Support Patients and Their Families in the Hospice Unit
June 25, 2015 updated by: Pesach Shvartzman
The increasing awareness of the importance of palliative care has led, in Israel, to the 2005 Law for the Rights of Persons with Terminal Illness.
Still, problems of accessibility to palliative care remain unresolved.
The use of e-health services is likely to expand the ability of the medical, psychosocial and nursing staff to reach patients who are either living in the periphery, are unable to make clinic visits or whose family members are housebound in order to be caregivers.
This exploratory research is designed to explore the issues, barriers and advantages of e-health care through the perspective of the palliative care staff members, the patients themselves and their caregiving family members.
Study Overview
Detailed Description
This study is designed to test the applicability and suitability of e-health services (e.g. by use of SKYPE) to the psychosocial needs of patients and their families who are getting services through home hospice care.
In addition, the attitudes of the hospice staff will be investigated to the use of e-health methods.
The study will clarify selection criteria, referral pathways and barriers and/or supporting elements that will allow e-health services to be provided in a highly professional fashion.
Up to 20 dyads of a patient and their primary caregiver will be recruited from those who are receiving services from the home hospice unit of the Kupat Holim Clalit (General Sick Fund) in the South of Israel.
Study Type
Interventional
Enrollment (Anticipated)
20
Phase
- Not Applicable
Contacts and Locations
This section provides the contact details for those conducting the study, and information on where this study is being conducted.
Participation Criteria
Researchers look for people who fit a certain description, called eligibility criteria. Some examples of these criteria are a person's general health condition or prior treatments.
Eligibility Criteria
Ages Eligible for Study
18 years and older (Adult, Older Adult)
Accepts Healthy Volunteers
No
Genders Eligible for Study
All
Description
Inclusion Criteria:
- Patient currently receiving care from the home hospice unit,
- over the age of 18,
- able to give informed consent,
- with a computer that can use SKYPE or a smartphone,
- speaking a language of the psychosocial staff person (Hebrew, English, Russian, Arabic).
Exclusion Criteria:
- Brain tumors,
- dementia,
- speech disturbance,
- refusal to participate,
- language other than the four spoken by psychosocial staff members,
- inability to use technology or lack of computer in the home.
Study Plan
This section provides details of the study plan, including how the study is designed and what the study is measuring.
How is the study designed?
Design Details
- Primary Purpose: Supportive Care
- Allocation: Non-Randomized
- Interventional Model: Single Group Assignment
- Masking: None (Open Label)
Arms and Interventions
Participant Group / Arm |
Intervention / Treatment |
|---|---|
|
Experimental: Intervention group: All dyads are in the intervention arm.
|
e-health services (e.g. by use of SKYPE) to the psychosocial needs of patients and their families who are getting services through home hospice care.
In addition, the attitudes of the hospice staff will be investigated to the use of e-health methods.
|
What is the study measuring?
Primary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
|---|---|---|
|
SWAT - The social work assessment tool
Time Frame: One year
|
Tool to assess the quality of social work psychosocial services
|
One year
|
Secondary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
|---|---|---|
|
EIS (Emotional Intimacy Scale)
Time Frame: 6 month
|
assess the emotional intimacy component a close relationship
|
6 month
|
|
SLDS (Satisfaction with cancer scale)
Time Frame: 6 month
|
assess cancer patient quality of life
|
6 month
|
|
the will to live question
Time Frame: 6 month
|
assess the will to live in a specific time point
|
6 month
|
|
ZBI (Zarit burden scale),
Time Frame: 6 month
|
assess primary care burden
|
6 month
|
|
attitudes toward use of e-therapy questionnaire.
Time Frame: 6 month
|
estimate attitudes of professional care giver
|
6 month
|
Collaborators and Investigators
This is where you will find people and organizations involved with this study.
Sponsor
Study record dates
These dates track the progress of study record and summary results submissions to ClinicalTrials.gov. Study records and reported results are reviewed by the National Library of Medicine (NLM) to make sure they meet specific quality control standards before being posted on the public website.
Study Major Dates
Study Start
June 1, 2015
Primary Completion (Anticipated)
May 1, 2016
Study Completion (Anticipated)
May 1, 2017
Study Registration Dates
First Submitted
June 10, 2015
First Submitted That Met QC Criteria
June 25, 2015
First Posted (Estimate)
June 26, 2015
Study Record Updates
Last Update Posted (Estimate)
June 26, 2015
Last Update Submitted That Met QC Criteria
June 25, 2015
Last Verified
June 1, 2015
More Information
Terms related to this study
Other Study ID Numbers
- ק007/2015
This information was retrieved directly from the website clinicaltrials.gov without any changes. If you have any requests to change, remove or update your study details, please contact register@clinicaltrials.gov. As soon as a change is implemented on clinicaltrials.gov, this will be updated automatically on our website as well.