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| Name | Class |
|---|---|
| Sociedad Española de Cuidados Paliativos SECPAL | UNKNOWN |
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This work aims to study the benefits that the therapeutic interview Kibo in palliative care patients can have for spirituality.
A parallel randomized controlled trial of two groups was performed. Information was collected on 60 palliative care patients during the moments before and after the intervention.
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| Label | Type | Description | Intervention Names |
|---|---|---|---|
| Control group | No Intervention | Group of participants that received usual psychological attention. | |
| Experimental group | Experimental | Group of participants that received usual psychological attention plus attention of spiritual needs following the Kibo protocol (intervention). |
|
| Name | Type | Description | Arm Group Labels | Other Names |
|---|---|---|---|---|
| Therapeutic interview: kibo protocol | Other | The kibo protocol is a therapeutic interview designed to address the spiritual needs of patients at the end of life. |
|
| Measure | Description | Time Frame |
|---|---|---|
| Change in the dimension of spirituality (PRE and POST measures) | This variable was assessed with the Spirituality questionnaire from the Spanish Society of Palliative Care (SECPAL). This questionnaire contains 8 items, and it provides scores from 0 to 32, where higher values represent a better outcome. In order to observe the change in the dimension of spirituality, it was measured at in two time points: First measurement: PRE. Once the participant had signed the informed consent, the initial score for this outcome was assessed. Second measurement: POST. Up to 4 weeks after the first measurement, the second measurement of the same variable was carried out. Between first and second measurement, the control group received the usual psychological attention, whereas the intervention group received usual psychological attention plus attention of spiritual needs following the Kibo protocol (intervention). | Baseline up to 4 weeks |
| Measure | Description | Time Frame |
|---|---|---|
| Change in resilience (PRE and POST measures) | This variable was assessed with the Brief Resilient Coping Scale (BRCS). This scale contains 4 items, and it provides scores from 4 to 20, where higher values represent a better outcome. In order to observe the change in the dimension of resilience, it was measured at in two time points: First measurement: PRE. Once the participant had signed the informed consent, the initial score for this outcome was assessed. Second measurement: POST. Up to 4 weeks after the first measurement, the second measurement of the same variable was carried out. Between first and second measurement, the control group received the usual psychological attention, whereas the intervention group received usual psychological attention plus attention of spiritual needs following the Kibo protocol (intervention). |
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Inclusion Criteria:
Exclusion Criteria:
a) Estimated time of survival: Patients with a life expectancy of two weeks or less will not be intervened.
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| Name | Affiliation | Role |
|---|---|---|
| Pilar Barreto Martin, PhD | Universitat de València | Principal Investigator |
| Facility | Status | City | State | ZIP | Country | Contacts |
|---|---|---|---|---|---|---|
| Universitat de València | Valencia | 46010 | Spain |
| PubMed Identifier | Type | Citation | Retractions |
|---|---|---|---|
| 32973614 | Derived | Soto-Rubio A, Perez-Marin M, Rudilla D, Galiana L, Oliver A, Fombuena M, Barreto P. Responding to the Spiritual Needs of Palliative Care Patients: A Randomized Controlled Trial to Test the Effectiveness of the Kibo Therapeutic Interview. Front Psychol. 2020 Aug 21;11:1979. doi: 10.3389/fpsyg.2020.01979. eCollection 2020. |
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| Baseline up to 4 weeks |
| Change in demoralization (PRE and POST measures) | This variable was assessed with the Short Demoralization Scale (SDS). This scale contains 5 items, and it provides scores from 0 to 20, where lower values represent a better outcome. In order to observe the change in the dimension of demoralization, it was measured at in two time points: First measurement: PRE. Once the participant had signed the informed consent, the initial score for this outcome was assessed. Second measurement: POST. Up to 4 weeks after the first measurement, the second measurement of the same variable was carried out. Between first and second measurement, the control group received the usual psychological attention, whereas the intervention group received usual psychological attention plus attention of spiritual needs following the Kibo protocol (intervention). | Baseline up to 4 weeks |