Cancer Clinical Trial
Official title:
Well-being Biomarkers and Psychological Functioning of Adult Patients During Chemotherapy Treatment: the Effects of Hospital Clowns and Hosting Conditions
Verified date | November 2023 |
Source | University of Coimbra |
Contact | n/a |
Is FDA regulated | No |
Health authority | |
Study type | Interventional |
The goal of this interventional study is to evaluate the impact of Hospital Clowns (HCs) intervention, besides to hospital hosting conditions, in the well-being of adult female patients during ambulatory chemotherapy. The main question[s] it aims to answer are: - Do the short-term HCs interventions during ambulatory chemotherapy may increase well-being of adult cancer patients in comparison to the hospital hosting conditions? - Do the short-term HCs interventions, besides the hospital hosting conditions, have effects on well-being biomarkers in association with psychological outcomes? Participants self-collect a sample of saliva followed by psychological assessment, at a first time-point (basal) and at a final time-point (~after 90 minutes of basal) (pre- and post-test), during the chemotherapy treatment session. Researchers have compared an HCs intervention plus hosting conditions - experimental group, EG, and hosting conditions only - control group, CG, by the repeated measures of pre- and post-test of biomarkers in saliva and the psychological functioning evaluations, to see the degree of the impact of HCs intervention in the well-being of the patients in comparison with normal hosting conditions. Each HCs intervention lasts around 15 minutes, and it is performed in the middle of the procedure between pre- and post-test.
Status | Completed |
Enrollment | 64 |
Est. completion date | August 28, 2020 |
Est. primary completion date | August 28, 2020 |
Accepts healthy volunteers | No |
Gender | Female |
Age group | 18 Years and older |
Eligibility | Inclusion Criteria: - Adult women with cancer undergoing chemotherapy in the ambulatory hospital Exclusion Criteria: - Patients with head and neck cancer - Having their first or last chemotherapy session - Receiving chemotherapy orally or via lumbar puncture - Presenting with any cognitive or language impairment that would prevent their understanding of the study and assessment or that could predictably interfere the levels of biomarkers evaluated |
Country | Name | City | State |
---|---|---|---|
Portugal | Instituto Português de Oncologia de Coimbra Francisco Gentil, E.P.E. | Coimbra | |
Portugal | University of Coimbra - Faculty of Psichology | Coimbra | |
Portugal | University of Coimbra - Laboratory of Mitochondrial Biomedicine and Theranostics | Coimbra |
Lead Sponsor | Collaborator |
---|---|
University of Coimbra | Portuguese Oncology Institute, Coimbra |
Portugal,
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* Note: There are 15 references in all — Click here to view all references
Type | Measure | Description | Time frame | Safety issue |
---|---|---|---|---|
Primary | Oxytocin levels (saliva) | Saliva collection for the biomarkers analysis was followed by psychological assessment, both at baseline (pre-test) and after ~90 minutes (post-test).
The procedure was similar for all participants, considering the HCs intervention duration of 15 minutes performed between the baseline (pre-test) and after ~90 minutes (post-test) in the EG. Saliva collections were performed by the participants themselves, following instructions and using Saliva Collection Aid Salimetrics (5016.02-SAL), and stored at 4°C. The evaluation of oxytocin levels was performed by using the colorimetric competitive enzyme immunoassay ELISA kit ADI-900-153A (Enzo Life Sciences). Oxytocin extraction was required prior to ELISA, using SPE columns, acetonitrile and trifluoroacetic acid, according to manufacturers' instructions. All the samples were analyzed in duplicate, the saliva oxytocin content was expressed in pg/mL, determined by plotting the optical density of each sample against the standard curve. |
Basal and after ~ 90 minutes, during the chemotherapy treatment session | |
Primary | Cortisol levels (saliva) | Saliva collection for the biomarkers analysis was followed by psychological assessment, both at baseline (pre-test) and after ~90 minutes (post-test).
The procedure was similar for all participants, considering the HCs intervention duration of 15 minutes performed between the baseline (pre-test) and after ~90 minutes (post-test) in the EG. Saliva collections were performed by the participants themselves, following instructions and using Saliva Collection Aid Salimetrics (5016.02-SAL). The samples were collected according to the schedule as described above and stored at 4°C. The evaluation of cortisol levels was performed by using the colorimetric competitive enzyme immunoassay ELISA kit ADI-900-071 (Enzo Life Sciences). The samples were thawed and centrifuged for immediate immunoassay processing in duplicate. A standard curve was used to estimate the cortisol content (pg/mL). |
Basal and after ~ 90 minutes, during the chemotherapy treatment session | |
Primary | Serotonin levels (saliva) | Saliva collection for the biomarkers analysis was followed by psychological assessment, both at baseline (pre-test) and after ~90 minutes (post-test).
The procedure was similar for all participants, considering the HCs intervention duration of 15 minutes performed between the baseline (pre-test) and after ~90 minutes (post-test) in the EG. Saliva collections were performed by the participants themselves, following instructions and using Saliva Collection Aid Salimetrics (5016.02-SAL) and stored at 4°C. In the serotonin determination, samples were concentrated by lyophilization. The samples were frozen in liquid nitrogen and then processed in a freeze dryer. The serotonin ELISA assay was performed using a colorimetric competitive enzyme immunoassay (ADI-900-175 (Enzo Life Sciences)) kit, following to manufacturers' directions. The optical density (OD) was red at ?=405nm and the serotonin content (ng/mL) was determined by plotting OD of each sample against the standard curve. |
Basal and after ~ 90 minutes, during the chemotherapy treatment session | |
Primary | ATP levels (saliva) | Saliva collection for the biomarkers analysis was followed by psychological assessment, both at baseline (pre-test) and after ~90 minutes (post-test).
The procedure was similar for all participants, considering the HCs intervention duration of 15 minutes made between the baseline (pre-test) and after ~90 minutes (post-test) in the EG. Saliva collections were performed by the participants themselves, following instructions and using Saliva Collection Aid Salimetrics (5016.02-SAL), according to the schedule described and stored at 4°C. The assessment of the saliva ATP levels was performed using a bioluminescent assay (ATP Bioluminescence Assay Kit HS II, Roche Diagnostics). This technique uses the ATP dependence on oxidation catalyzed by luciferase and allows the measurement of extremely low concentrations of ATP (up to 10-15 mol) in the saliva samples. The protein concentration was assayed by the Bradford method, and ATP levels were expressed normalized to that concentration. |
Basal and after ~ 90 minutes, during the chemotherapy treatment session | |
Secondary | Positive Affect (PA) | Psychological assessment was performed after saliva collection, both at baseline (pre-test) and after ~90 minutes (post-test).
The procedure was similar for all participants, considering the HCs intervention duration of 15 minutes performed between the baseline (pre-test) and after ~90 minutes (post-test) in the EG. Affectivity was assessed by the Positive and Negative Affect Schedule (PANAS). The PANAS has two independent subscales with five items each. Responses are in a Likert scale and can vary from 1 ("Nothing or very slightly") to 5 ("Extremely"). The PANAS can measure affective and mood states in the moment. Higher values in positive affect (PA) and lower values in negative affect (NA) correspond, respectively, to a better affectivity. The Portuguese adaptation showed good psychometric properties, internal consistency (Cronbach's alpha =0.86 for PA) and 0.89 for NA) and structural validity through Confirmatory Factor Analysis. |
Basal and after ~ 90 minutes, during the chemotherapy treatment session | |
Secondary | Negative Affect (NA) | Psychological assessment was performed after saliva collection, both at baseline (pre-test) and after ~90 minutes (post-test).
The procedure was similar for all participants, considering the HCs intervention duration of 15 minutes performed between the baseline (pre-test) and after ~90 minutes (post-test) in the EG. Affectivity was assessed by the Positive and Negative Affect Schedule (PANAS). The PANAS has two independent subscales with five items each. Responses are in a Likert scale and can vary from 1 ("Nothing or very slightly") to 5 ("Extremely"). The PANAS can measure affective and mood states in the moment. Higher values in positive affect (PA) and lower values in negative affect (NA) correspond, respectively, to a better affectivity. The Portuguese adaptation showed good psychometric properties, internal consistency (Cronbach's alpha =0.86 for PA) and 0.89 for NA) and structural validity through Confirmatory Factor Analysis. |
Basal and after ~ 90 minutes, during the chemotherapy treatment session | |
Secondary | Emotional States (PESS) | Psychological assessment was performed after saliva collection, both at baseline (pre-test) and after ~90 minutes (post-test).
The procedure was similar for all participants, considering the HCs intervention duration of 15 minutes performed between the baseline (pre-test) and after ~90 minutes (post-test) in the EG. Emotional States were assessed by the Perception of Emotional States Scale (PESS), based on semantic differential scales and consisting of 8 pairs of opposite adjectives separated by 7 positions (e.g., calm/nervous; happy/sad). These pairs were selected because they represent emotional states, different from the affective states assessed by PANAS. Lower ratings correspond to a better emotional state. |
Basal and after ~ 90 minutes, during the chemotherapy treatment session | |
Secondary | Cognitive and Affective Mindfulness (CAMS-R) | Psychological assessment was performed after saliva collection, both at baseline (pre-test) and after ~90 minutes (post-test).
The procedure was similar for all participants, considering the HCs intervention duration of 15 minutes performed between the baseline (pre-test) and after ~90 minutes (post-test) in the EG. Cognitive and Affective Mindfulness was measured by the Cognitive and Affective Mindfulness Scale-Revised (CAMS-R), having 9 items rated to a 4-point Likert scale, ranging from 1 (Not at all) to 4 (A lot) and measures mindfulness qualities of attention, tolerance and acceptance of the present moment, with higher values corresponding to better results. For the present study, only 6 items were considered, because of the need to make the psychological assessment as brief as possible so that a minimum interference with ambulatory sessions functioning would occur and respecting the patient's availability could be ensured. |
Basal and after ~ 90 minutes, during the chemotherapy treatment session | |
Secondary | Cognitive functioning (CDT) | Psychological assessment was performed after saliva collection, both at baseline (pre-test) and after ~90 minutes (post-test).
The procedure was similar for all participants, considering the HCs intervention duration of 15 minutes performed between the baseline (pre-test) and after ~90 minutes (post-test) in the EG. Cognitive functioning was assessed by the Clock-Drawing Test (CDT, with higher values corresponding to better cognitive functioning). The CDT measures visuospatial, visuoconstructive and visuomotor capabilities. This test also evaluates other cognitive functions, including language/understanding, memory, attention and executive functions (planning, organization, simultaneous processing, self-monitoring). It is commonly used as a brief cognitive screening test. The Portuguese version of the 18-point quantitative scoring system was used. |
Basal and after ~ 90 minutes, during the chemotherapy treatment session | |
Secondary | Satisfaction with HCs' intervention | Satisfaction with HCs' intervention was evaluated in EG through two single items: (1) "Do you think this type of interventions in the hospital is important?", answered on a 4-point Likert scale (ranging between "Very important" and "Nothing important"); and (2) "How satisfied are you with the intervention of the HCs that you just saw?" answered in a 5-point Likert scale (ranging between "Very Satisfied" and "Very Unsatisfied"). | After ~ 90 minutes from basal, during the chemotherapy treatment session |
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