Clinical trial · Interventional
Effect of the Nursing Intervention "Spiritual Support"
Effect of the Nursing Intervention "Spiritual Support" in the Level of Spirituality and Clinical Parameters in Women With Breast Cancer: a Randomized Clinical Trial
- 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)
Condition: patients with breast cancer. Intervention: spiritual support (relaxation + image guided + meditation) or relaxation in three consecutive meetings (day 2, 3 and 4), three days of intervention in the same week. The first day the participants will be evaluated if she meets the needs of the research and will answer questions about their indentification and spirituality. Type of study: intervention Study design: randomized controlled trial Masking: blind study. Randomization: sequence generated by SPSS (Statistical Package for the Social Sciences) version 15, organized in sealed envelopes by another qualified professional. The research ends in 2014 jun.
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 |
|---|---|---|---|
| Breast Neoplasms | Breast Neoplasm | ONTOLOGY_EXACT | 0.98 |
Interventions
Interventions (2)
| Intervention | Type | Mapped drug | Match |
|---|---|---|---|
| relaxation therapy | Behavioral | — | UNRESOLVED |
| spiritual support | Behavioral | — | UNRESOLVED |
Design
Arms and outcomes
Arms (2)
- type
- EXPERIMENTAL
- label
- spiritual support
- description
- -Spiritual Support: deep breathing + guided image + meditation Each patient will participate individually in three sequential meetings (A1, A2 and A3). In the experimental group, it will be developed the support spiritual intervention in all three meetings. In all meetings, namely A1, A2 and A3 the physiological parameters will be recorded (PA, SpO2, HR) through the monitor BM5.
- interventionNames
- Behavioral: spiritual support
- type
- ACTIVE_COMPARATOR
- label
- relaxation therapy
- description
- Relaxation Therapy Each patient will participate individually in three sequential meetings (A1, A2 and A3). In the control group, it will be performed just relaxing in all three meetings. In all meetings, namely A1, A2 and A3 the physiological parameters will be recorded (PA, SpO2, HR) through the monitor BM5.
- interventionNames
- Behavioral: relaxation therapy
Primary outcomes (1)
Eligibility
Eligibility (as posted)
- Sex
- Female
- Minimum age
- 18 Years
Show eligibility criteria text
Inclusion Criteria: * Diagnosis of breast cancer (record of inclusion and monitoring); * Patients in follow up treatment for breast cancer (record of inclusion and monitoring); * Have more than 18 years (record of inclusion and monitoring); Exclusion Criteria: * Present history of psychiatric disorders involving hallucinations (record of inclusion and monitoring). * Present energy-reduction (Eastern Cooperative Oncology Group - ECOG/Zubrod Scale) - ECOG greater than 3 * Present decreased cognition (Mini-Mental State Examination MMSE/Brucki et al. 2003) - lower sum related to grade school.
References
Publications (0)
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