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

Status

Unknown

Conditions

Intervention / Treatment

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.

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.

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