Clinical trial · Interventional
e-Natureza Project - Affective Validation of Nature Images for Hospital Use
e-Natureza: Affective Validation of Nature Images as a Complementary Resource for Promoting Well-being in Hospital Environment
NCT03518255CI-TRIAL-00049969E-naturezacompletedN/AClinicalTrials.gov clinicaltrialsProvenance
- Source
- ClinicalTrials.gov
- Retrieved
- Sep 8, 2026
- Layer
- normalized (units and labels harmonized; values unchanged)
- Run
- ING-CLINICALTRIALS-20260908-000001
Summary
Brief summary (as posted)
Randomized clinical trial about the evaluation of the use of nature photographs in the positive and negative affects of oncological patients.
Conditions
Conditions (1)
Free-text conditions as registered, with the CancerIndex entity they were reconciled to and the match type.
| Condition (as posted) | Mapped entity | Match | Confidence |
|---|---|---|---|
| Cancer | Malignant Neoplasm | ALIAS | 0.90 |
Interventions
Interventions (1)
| Intervention | Type | Mapped drug | Match |
|---|---|---|---|
| Nature video | Other | — | UNRESOLVED |
Design
Arms and outcomes
Arms (2)
- type
- NO_INTERVENTION
- label
- Control group
- description
- This control group will not receive an intervention.
- type
- EXPERIMENTAL
- label
- Nature video
- description
- A pre-validated nature images video will be shown to the patient during their chemotherapy session. After thirty minutes of the start of the chemotherapy session, the patient you will receive a notebook (specific to the study and blocked for other functions) that he can watch a presentation of nature images. It will be four videos with fifteen minutes each one.
- interventionNames
- Other: Nature video
Primary outcomes (1)
- measure
- Positive and Negative Affect Schedule (PANAS)
- timeFrame
- Change from Baseline positive and negative affects at immediate post intervention, through study completion, an average of 1 year
Eligibility
Eligibility (as posted)
- Sex
- All
- Minimum age
- 18 Years
Show eligibility criteria text
Inclusion Criteria: * Voluntary participation; * Signed in the Informed Consent Form; * Who are undergoing chemotherapy treatment; * Patients need to be on the first chemotherapy session, independently of oncological disease; * Patients with clinical conditions and preserved communication function, in other words, lucid patients. Exclusion Criteria: * Blind patients; * Patients without the capacity for judgment, in other words, with dementia; * Patients who have their clinical condition aggravated during the chemotherapy session.
References
Publications (1)
- BACKGROUNDLeao ER, Dal Fabbro DR, Oliveira RB, Santos IR, Victor ED, Aquarone RL, Andrade CB, Ribeiro VF, Oliveira RC, Friedlander R, Ferreira DS. Stress, self-esteem and well-being among female health professionals: A randomized clinical trial on the impact of a self-care intervention mediated by the senses. PLoS One. 2017 Feb 27;12(2):e0172455. doi: 10.1371/journal.pone.0172455. eCollection 2017. PMID 28241070