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HopeNCT07113899

HOPE AND ACCEPTANCE AT THE END OF LIFE - IMPACT OF SPIRITUALITY ON PALLIATIVE CARE PATIENTS

A study testing Approach to spirituality through hope and acceptance in people with Hope and Acceptance, run by Unidade Local de Saúde de Coimbra, EPE at 1 site in Portugal.

Completed

Finished. The study has ended and is not enrolling. Results may be posted on the official record.

Official record

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Trial summary

This study aims to evaluate the hope and acceptance among patients visited by the Equipa Comunitária de Suporte em Cuidados Paliativos do Baixo Mondego. This study is a prospective longitudinal research study. Read more about this study

Who is it for?
Ages 18 years and older
Conditions the study is for
Hope, Acceptance, Spirituality
What is being tested?
Approach to spirituality through hope and acceptance
Could I receive a placebo?
No, everyone receives an active treatment
How many people
20 participants
Where
1 sitePortugal
Study dates
1 Jan 2025to 31 May 2025
Phase
Interventional

Key requirements

Who can take part, as listed by the sponsor. Only the study team can confirm whether you are eligible, so take this list to your doctor.

  • Ages 18 years and older
  • All sexes
  • No healthy volunteers
  • Adult, Older adult

Who may be able to join

  • new referrals made by the family doctor to the community palliative care support team (which integrated the patient into the palliative care team network for the first time) - for the intervention group
  • patients registered at the Nautilus Family Health Unit or Coimbra Centro Family Health Unit with serious pathology, comorbidities and reserved prognosis - for the control group

Who cannot join

  • age under 18
  • pregnancy
  • altered state of consciousness or dementia
  • low level of education

Trial locations and contacts

1 site in 1 country.

Portugal1 site
  • Lutenio Soares Faria Junior

    Coimbra, Coimbra District, 3000-317

Other trials in Portugal

About this study

This study aims to evaluate the hope and acceptance among patients visited by the Equipa Comunitária de Suporte em Cuidados Paliativos do Baixo Mondego. This study is a prospective longitudinal research study. The sample consisted of two groups: the Intervention Group, which included patients from the network of the Equipa Comunitária de Suporte em Cuidados Paliativos do Baixo Mondego (ECSCP-BM), and the Control Group, with selected patients from Unidade de Saúde Familiar Nautilus e Unidade de Saúde Familiar Coimbra Centro, with serious illness, comorbidities, and a poor prognosis. The patients chosen from ECSCP-BM were made up only of new patients referred to the team without any prior home consultations. The first questionnaire application took place during the first visit, and the second one was administered fourteen days later. The Primary Health Care patients were selected by invitation, and the questionnaire was administered. It included sociodemographic data, clinical data, the Herth Hope Index - PT and open questions.

Being tested
Approach to spirituality through hope and acceptance
Keywords
hope, acceptance, spirituality, end of life, palliative care
Medical subject headings
Death

What participants receive

What participants receive. In a randomised study each person is assigned to one group by chance.

  • Approach to spirituality through hope and acceptanceOther

    This study is a prospective longitudinal research study. The sample consisted of two groups: the Intervention Group, which included patients from the community palliative care support team (ECSCP-BM), and the Control Group, with primary health care selected patients from the family health units Nautilus and Coimbra Centro (CSP), with serious illness, comorbidities, and a poor prognosis. The patients chosen from ECSCP-BM were made up only of new patients referred to the team without any prior home consultations. The first questionnaire application took place during the first visit, and the second one was administered fourteen days later. The Primary Health Care patients were selected by invitation, and the questionnaire was administered. It included sociodemographic data, clinical data, the Herth Hope Index and open questions.

    During the palliative care team's home visit, spirituality was addressed in in the clinical history through the assessment of hope and acceptance.

Study groups in NCT07113899
Study groupRoleWhat they receive
ECSCPExperimentalPatients visited at home by the community palliative care support team
Receives: Other: Approach to spirituality through hope and acceptance
CSPNo interventionPatients with follow-up consultations by primary health care

What is being measured

The primary outcome is the main question the study is designed to answer.

  1. Hope

    Participants answered questions on the Hope Scale. There were 9 questions with 4 possible answers. Each answer was scored from 1 to 4. The maximum score on the scale was 36.

    Measured: 5 months

  2. Acceptance

    Participants answered three open-ended questions to assess their acceptance. These questions were asked to the control group and at the first assessment of the intervention group. At the second assessment of the intervention group, after 14 days, a fourth question was also asked, assessing the team's intervention during those 14 days.

    Measured: 5 months

Timeline

From the start of the study to its completion; the mark is today. Estimated dates are the sponsor’s plan.

  1. First posted11 Aug 2025
  2. Study start1 Jan 2025
  3. Primary completion31 May 2025
  4. Study completion31 May 2025

Resources

More details

For doctors and researchers: how the study is designed, who runs it, and its registry IDs.

Study design
Study type
Interventional
Phase
Phase N/A
Primary purpose
Health services research
Allocation
Non-randomised
Intervention model
Parallel groups
Masking
Single blind
Who is masked
Participant
Enrolment
20 participants (actual)
IDs, dates and publications
ClinicalTrials.gov ID
NCT07113899
Sponsor's protocol ID
CE-190/2024
Status last verified
Dec 2024
First submitted
3 Aug 2025
Last updated
11 Aug 2025
Results posted
No
Data monitoring committee
No
FDA-regulated drug
No
FDA-regulated device
No

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