Quality of Life Clinical Trial
Official title:
Study With Cancer Patients at the CECON Foundation's Pain Therapy and Palliative Care Service: Meditation With Immersive Virtual Reality for Pain Relief
Cancer is a disabling, challenging and growing global disease. Although early diagnosis and adequate treatment of oncological disease have been developing rapidly, a large part of the population remains without access to specialized services and routinely evolve to symptoms and sequelae with uncontrolled pain, worse quality of life and suffering. Complementary therapies to control pain and improve the well-being of cancer patients are fundamental tools of integrative oncology medicine. This study proposes to use immersive virtual reality to encourage cancer patients to carry out the regular practice of meditation, as an effective tool in pain management and in the search for a better quality of life, based on a structured intervention that encourages autonomy as important part of your treatment. Two studies will be carried out at the Pain Therapy and Palliative Care Service of the Amazonas State Oncology Control Center Foundation (FCECON). Study 1 will be a cross-sectional study to describe the variables associated with the diagnosis and treatment of patients' pain and Study 2 will be a Randomized Controlled Trial that will analyze the impact of an intervention performed with meditation through immersive virtual reality for pain relief. pain in these patients. It is expected that the regular practice of meditation through immersive virtual reality will promote pain relief and improve the quality of life of cancer pain patients.
Status | Not yet recruiting |
Enrollment | 129 |
Est. completion date | August 30, 2025 |
Est. primary completion date | June 30, 2025 |
Accepts healthy volunteers | No |
Gender | All |
Age group | 18 Years to 75 Years |
Eligibility | Inclusion Criteria: - Be followed up at the Pain Therapy and Palliative Care Service (STDCP) to control symptoms resulting from any type of cancer at any stage; - Have a diagnosis of chronic pain, recorded in the medical records. - Be between 18 and 75 years old on the date of the first collection; - Be able to understand Portuguese (read and write); - Have normal vision and hearing; - Have a cell phone with an Android system; - Be able to make head movements and have sufficient motor control to make body movements; - Agree to take part in the study and sign the Informed Consent Form (ICF). Exclusion Criteria: - Indigenous patients (due to cultural and linguistic peculiarities and special legislation); - Patients with records of serious psychiatric illnesses (DSM-5 - Diagnostic and Statistical Manual of Mental Disorders - schizophrenia, schizotypal disorders, delusional disorders, borderline and dementias); - Impairment of the ability to understand or communicate based on the researcher's assessment; - Report of discomfort with the use of Immersive Virtual Reality; - Progression of the disease with limitation in maintaining the proposed regular outpatient visits; - Patients with brain tumors, brain metastases or a previous history of seizures. |
Country | Name | City | State |
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n/a |
Lead Sponsor | Collaborator |
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Emily Santos Montarroyos | AC Camargo Cancer Center |
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* Note: There are 16 references in all — Click here to view all references
Type | Measure | Description | Time frame | Safety issue |
---|---|---|---|---|
Primary | Brief Pain Inventory (Reduced version) | It has a body schema, in which the patient can mark the location of the pain, as well as 8 questions relating to pain intensity, on a scale of 0 to 10, the higher the score on the inventory, the worse the pain intensity. | six months | |
Primary | McGill Quality of Life Questionnaire | Made up of 16 items, divided into domains: physical well-being, psychological well-being, existential well-being, support and physical symptoms. It has a single-item scale that measures overall quality of life, which is not included in the score, but is used to compare scores. It also has an open question for the patient to name the things that have had the greatest effect on their quality of life. The scale has eleven points from 0 to 10, and the higher the final score, the better the quality of life. | six months | |
Secondary | Hospital Anxiety and Depression Scale (HADS) | A 14-item instrument with two sub-scales, anxiety and depression, with seven items each to assess depression and anxiety. The score for each item can vary from zero to three, with a maximum score of 21 points for each sub-scale (anxiety and depression). Patients with no anxiety/depression are considered to score from 0 to 8, and = 9 have anxiety/depression. | six months | |
Secondary | The Edmonton Symptom Assessment Scale (ESAS) | The ESAS is a simple, self-reported questionnaire designed to indicate objective and subjective symptoms. On this scale, the patient or their caregiver/family member assigns a score from 0 to 10 for each symptom, with 0 being the absence and 10 the greatest intensity of the symptom. | six months | |
Secondary | The National Comprehensive Cancer Network® (NCCN) Distress Thermometer | The National Comprehensive Cancer Network® (NCCN) Distress Thermometer will be applied as a questionnaire during the 3 moments. It is a translated and validated NCCN tool used to measure the "temperature" of the mental health of people with cancer. The Brazilian version of the NCCN Distress Thermometer and Problem List. | six months |
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