Hope Promotion Program: Effectiveness in Palliative Patients (HPP)
Primary Purpose
Chronically Ill
Status
Completed
Phase
Not Applicable
Locations
Study Type
Interventional
Intervention
Hope Promotion Program (HPP)
Standard Treatment Protocol
Sponsored by
About this trial
This is an interventional supportive care trial for Chronically Ill focused on measuring Hope, Quality of Life, Comfort
Eligibility Criteria
Inclusion Criteria:
- Portuguese speaking
- Have a chronic advanced disease non-responding to treatment, metastatic disease, episodes of non-controlled symptoms
- Have health care assistance by a health care team in an outpatient setting
- Cognitive ability to answer the questionnaires (MMSE>15 for illiterate participants, >22 for participants with 11 years of schooling, >27 for participants with more than 11 years of schooling)
- Consenting to voluntarily participate in the study.
Exclusion Criteria:
- Patients with high suffering from uncontrolled and recurrent presence of symptoms (nausea, vomiting, pain),
- Patients with performance status under 30, due to their particularly vulnerability, intervention would need energy required to vital functions.
Sites / Locations
Arms of the Study
Arm 1
Arm 2
Arm Type
Experimental
Other
Arm Label
Hope Promotion Program (HPP)
Standard Treatment Protocol
Arm Description
Plus to the standard treatment protocol, all the participants in this group attend the HPP, consisting of a three individual session's carried out by the nurse in patients' homes. It includes viewing the film Hopeful Living, enrolling in a hope activity from the Hope activity book, a relaxation activity and a negotiated plan to exercise hope in a regular basis.
Participants in this group has not access to a hope intervention. Data collection for outcome variables is the same as the participants in the other arms.
Outcomes
Primary Outcome Measures
Hope measured by the Portuguese version of Herth Hope Index
Hope is measured by the Portuguese version of Herth Hope Index for chronic conditions (HHI-PT-DC). The HHI-PT-DC is a 10 item (1-4 point) Likert scale that delineates two sub-scales of hope: a) temporality, trust and interconnection, b) positive readiness and expectancy. The HHI-PT-DC takes approximately 5 minutes to complete. Summative scores range from 10-40, with a higher score denoting greater hope.
Secondary Outcome Measures
Comfort measured by Portuguese version of Hospice Comfort Questionnaire
Comfort is measured by Portuguese version of Hospice Comfort Questionnaire, based on holistic comfort questionnaire, developed by Kolcaba (HCQ-PT-DC). This instrument is composed by 26 items (1-6 points) Likert-scale that addresses the three states of comfort: relief, ease and transcendence. The higher the score, the higher the subjects' reported comfort.
Quality of Life measured by the Portuguese version of McGill Quality of Life Questionnaire (MQOL-PT-DC)
Quality of Life is measured by the Portuguese version of McGill Quality of Life Questionnaire (MQOL-PT-DC). The MQOL-PT-DC is a quality of life assessment measure reflecting 4 domains of quality of life: physical health, psychological symptoms, existential well-being, and support. The MQOL-PT-DC is comprised of 16 items, assessed in a self-rating numerical scale (0-10) and Single Item Scale (0-10) to assess subjective quality of life. Higher scores indicates better QOL.
Full Information
NCT ID
NCT02723799
First Posted
March 14, 2016
Last Updated
January 5, 2023
Sponsor
Instituto Politécnico de Leiria
Collaborators
Universidade Católica Portuguesa
1. Study Identification
Unique Protocol Identification Number
NCT02723799
Brief Title
Hope Promotion Program: Effectiveness in Palliative Patients
Acronym
HPP
Official Title
Promoting Hope at the End of Life: Effectiveness of a Hope Intervention Program in Palliative Patients
Study Type
Interventional
2. Study Status
Record Verification Date
January 2023
Overall Recruitment Status
Completed
Study Start Date
January 2012 (undefined)
Primary Completion Date
July 2012 (Actual)
Study Completion Date
October 2013 (Actual)
3. Sponsor/Collaborators
Responsible Party, by Official Title
Principal Investigator
Name of the Sponsor
Instituto Politécnico de Leiria
Collaborators
Universidade Católica Portuguesa
4. Oversight
Data Monitoring Committee
No
5. Study Description
Brief Summary
This study aims to:
I. Develop and pilot test the effectiveness of a Hope Promotion Program compared with the standard treatment protocol, in hope, comfort and quality of life, based on a population of palliative patients followed at Oncology day care unit.
II. Evaluate perceptions and acceptability of Hope Promotion Program among palliative patients submitted to the intervention program.
Detailed Description
Background: Hope is essential in the experience of living with advanced chronic disease. Maintaining hope in situations of physical, psychological, spiritual and social suffering requires expertise and can be very difficult to achieve without the help of professionals, leading to hopelessness, despair and desire to hasten death (Rodin et al., 2007;Breitbart, 2000; Monforte-Royo, et al., 2012) The research team has designed an intervention program - Hope Promotion Program (HPP) to increase hope, comfort and quality of life in palliative patients. HPP consists of a three session's individual interventions carried out by the researcher in patients homes. The first session includes viewing the film Hopeful Living, produced by the research team, inspired by Duggleby et al, (2007) which features palliative patients, caregivers and health professionals describing their experiences of hope. The second session consists of patients' expression of feelings and emotions related with experience of living with a chronic advanced disease and the choice of a hope activity from the Hope activity book - a collection of hope activities specially designed for people living with an advanced chronic disease. The third session includes a relaxation activity and a plan to include hope exercise in patients' activities of daily living.
This project was designed according to the literature review of hope interventions and have the potential to become part of palliative care interventions evidenced based.
Aims: The purpose of this study is to evaluate the acceptability and feasibility and collect preliminary data on the effectiveness of the Hope Promotion Program for persons in palliative situation residing at home.
Moreover this project will allow to a) Obtain relevant information about hope, comfort and quality of life of palliative patients; b) Tailor therapeutic strategies to individual needs; c) increase hope, comfort and quality of life in patients at the end of life.
Sample: Patients with a chronic advanced disease in palliative situation, recruited from Oncology day care units of two district hospital in the centre of Portugal. Inclusion criterion for participants are: a) 18 years of age and older, b) Portuguese speaking, c) have cognitive capacity to participate in the study (MMSE>15) and d) have agreed to participate in the study. An interview with a nurse precede the inclusion in the study to explain the study and obtain written informed consent.
Design: This study is designed as a mix-methods randomized clinical trial (Quantitative +Qualitative) design. Patients eligible, are randomly assigned to one of two groups: 1) treatment (Hope Promotion Program delivered by a nurse in three sessions during one week), 2) usual care group.
In all groups, demographic information and measures of hope (Herth Hope Index), quality of life (McGillQOL), Comfort (Hospice Comfort Questionnaire) will be collected by a trained research nurse at baseline, day 15 and one month. Participants in group 1 (treatment group) will be asked to describe what they were thinking about when doing the hope activities on day 15 and one month using qualitative interviews. At one month all participants will be interviewed using open ended audiotaped questions to help evaluate the program and study procedures.
6. Conditions and Keywords
Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Chronically Ill
Keywords
Hope, Quality of Life, Comfort
7. Study Design
Primary Purpose
Supportive Care
Study Phase
Not Applicable
Interventional Study Model
Parallel Assignment
Masking
Participant
Allocation
Randomized
Enrollment
26 (Actual)
8. Arms, Groups, and Interventions
Arm Title
Hope Promotion Program (HPP)
Arm Type
Experimental
Arm Description
Plus to the standard treatment protocol, all the participants in this group attend the HPP, consisting of a three individual session's carried out by the nurse in patients' homes. It includes viewing the film Hopeful Living, enrolling in a hope activity from the Hope activity book, a relaxation activity and a negotiated plan to exercise hope in a regular basis.
Arm Title
Standard Treatment Protocol
Arm Type
Other
Arm Description
Participants in this group has not access to a hope intervention. Data collection for outcome variables is the same as the participants in the other arms.
Intervention Type
Behavioral
Intervention Name(s)
Hope Promotion Program (HPP)
Intervention Description
HPP is based on literature review and qualitative research in hope at the end-of-life. The film "Hopeful living" reflects the findings of the grounded theory study. Hope activity book is the final product of the literature review on hope interventions and its activities were tested in their feasibility and suitability in our previous research with persons with advanced cancer and their families.
Intervention Type
Other
Intervention Name(s)
Standard Treatment Protocol
Intervention Description
Regular assessment and care by the hospital outpatient health care team.
Primary Outcome Measure Information:
Title
Hope measured by the Portuguese version of Herth Hope Index
Description
Hope is measured by the Portuguese version of Herth Hope Index for chronic conditions (HHI-PT-DC). The HHI-PT-DC is a 10 item (1-4 point) Likert scale that delineates two sub-scales of hope: a) temporality, trust and interconnection, b) positive readiness and expectancy. The HHI-PT-DC takes approximately 5 minutes to complete. Summative scores range from 10-40, with a higher score denoting greater hope.
Time Frame
Change from baseline at day 15 and 30
Secondary Outcome Measure Information:
Title
Comfort measured by Portuguese version of Hospice Comfort Questionnaire
Description
Comfort is measured by Portuguese version of Hospice Comfort Questionnaire, based on holistic comfort questionnaire, developed by Kolcaba (HCQ-PT-DC). This instrument is composed by 26 items (1-6 points) Likert-scale that addresses the three states of comfort: relief, ease and transcendence. The higher the score, the higher the subjects' reported comfort.
Time Frame
Change from baseline at day 15 and 30
Title
Quality of Life measured by the Portuguese version of McGill Quality of Life Questionnaire (MQOL-PT-DC)
Description
Quality of Life is measured by the Portuguese version of McGill Quality of Life Questionnaire (MQOL-PT-DC). The MQOL-PT-DC is a quality of life assessment measure reflecting 4 domains of quality of life: physical health, psychological symptoms, existential well-being, and support. The MQOL-PT-DC is comprised of 16 items, assessed in a self-rating numerical scale (0-10) and Single Item Scale (0-10) to assess subjective quality of life. Higher scores indicates better QOL.
Time Frame
Change from baseline at day 15 and 30
10. Eligibility
Sex
All
Minimum Age & Unit of Time
18 Years
Accepts Healthy Volunteers
No
Eligibility Criteria
Inclusion Criteria:
Portuguese speaking
Have a chronic advanced disease non-responding to treatment, metastatic disease, episodes of non-controlled symptoms
Have health care assistance by a health care team in an outpatient setting
Cognitive ability to answer the questionnaires (MMSE>15 for illiterate participants, >22 for participants with 11 years of schooling, >27 for participants with more than 11 years of schooling)
Consenting to voluntarily participate in the study.
Exclusion Criteria:
Patients with high suffering from uncontrolled and recurrent presence of symptoms (nausea, vomiting, pain),
Patients with performance status under 30, due to their particularly vulnerability, intervention would need energy required to vital functions.
12. IPD Sharing Statement
Plan to Share IPD
No
Citations:
PubMed Identifier
35802350
Citation
Ryan RE, Connolly M, Bradford NK, Henderson S, Herbert A, Schonfeld L, Young J, Bothroyd JI, Henderson A. Interventions for interpersonal communication about end of life care between health practitioners and affected people. Cochrane Database Syst Rev. 2022 Jul 8;7(7):CD013116. doi: 10.1002/14651858.CD013116.pub2.
Results Reference
derived
Learn more about this trial
Hope Promotion Program: Effectiveness in Palliative Patients
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