Hospice Volunteer Community,Dying Patient Prepare Spirtal Care (volunteer)

June 10, 2024 updated by: National Taiwan University Hospital

Pathways to Hospice Volunteering: a Grounded Theory Study

Due to the aging population, the cases of elderly disability and death caused by chronic diseases and cancer are also increasing; thus increasing the demand and trend of community palliative care. Anning volunteers are members of the Anning team and play an integral role in the care of the "whole community". Partners who can provide psychosocial support in fear, grief, informal care, and "individualized care" can focus on patient and family needs and give their time and presence. And make up for the shortage of medical manpower. Assist nurses to take care of patients together, which is an important support for nursing care. In the community, An Ning volunteers are an important help to closely care for patients and support family members to take care of them at home and fulfill their wish of dying at home. In view of the community's peaceful home care, the trend and importance of hospice at home, it is necessary to cooperate with the "volunteers" of the tranquility team. Inquiry Only a few papers mentioned Anning volunteers' service history and research on the meaning of life, but there was a lack of in-depth and systematic discussions on Anning volunteers, including their motivation, training, process, care effectiveness, impact on training volunteer organization management, and volunteer retention. Therefore, the motivation of the research was aroused, and it was hoped to use grounded theory to explore the motivation and process of becoming an Anning volunteer, and to identify related concepts, and finally establish a theoretical framework to describe the relevant decision-making mentality. Also serves as a reference for volunteer organization management training and retention of palliative care volunteers.

Study Overview

Status

Active, not recruiting

Detailed Description

The purpose of this study is to use grounded theory to explore the motivation and process of becoming a tranquility volunteer, identify relevant concepts, and finally establish a theoretical framework to describe the relevant decision-making process.

This study adopts semi-structured in-depth interviews and semi-structured one-on-one interviews to collect data. During the interview process, according to the actual situation, the interview questions will be flexibly fine-tuned according to the data analysis results.

The data coding of grounded theory is divided into three levels: open decoding, axial decoding and selective decoding; through these three levels of coding, the data are decomposed, compared, conceptualized and integrated, and finally a theory is formed.

Study Type

Observational

Enrollment (Estimated)

30

Contacts and Locations

This section provides the contact details for those conducting the study, and information on where this study is being conducted.

Study Locations

      • Taipei county, Taiwan, 100
        • Nation Taiwan university hospictal

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

  • Adult
  • Older Adult

Accepts Healthy Volunteers

Yes

Sampling Method

Probability Sample

Study Population

Community hospice volunteers

Description

Inclusion Criteria:

  1. Adults aged 18 or above (2) Community hospice volunteers, who have served for more than one year (including one year), are currently serving volunteers or have stopped serving volunteers (3) Can speak Mandarin or Taiwanese communicate.

Exclusion Criteria:

  • Those who could not understand or conduct the interview due to any physical or psychological or cognitive factors were excluded.
  • no Dmentia stroke

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

Cohorts and Interventions

Group / Cohort
hospice volunteer
Pathways to hospice volunteering: a grounded theory study

What is the study measuring?

Primary Outcome Measures

Outcome Measure
Measure Description
Time Frame
Pathways to hospice volunteering: a grounded theory study bason interview interview The 60-minute in week 24
Time Frame: base on week 24
Using qualitative research to interview volunteers' motivations, journeys and training processes as volunteers
base on week 24

Collaborators and Investigators

This is where you will find people and organizations involved with this study.

Investigators

  • Principal Investigator: Chia-Chun Tang, PHD, professer

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 (Actual)

April 29, 2023

Primary Completion (Actual)

June 15, 2023

Study Completion (Estimated)

December 31, 2024

Study Registration Dates

First Submitted

May 1, 2023

First Submitted That Met QC Criteria

May 21, 2024

First Posted (Actual)

May 29, 2024

Study Record Updates

Last Update Posted (Actual)

June 12, 2024

Last Update Submitted That Met QC Criteria

June 10, 2024

Last Verified

April 1, 2024

More Information

Terms related to this study

Other Study ID Numbers

  • 202303083RINC

Plan for Individual participant data (IPD)

Plan to Share Individual Participant Data (IPD)?

UNDECIDED

IPD Plan Description

Possibility to give back to training institution results

Drug and device information, study documents

Studies a U.S. FDA-regulated drug product

No

Studies a U.S. FDA-regulated device product

No

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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