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Enrolling by invitation NCT07357207

Video-immunotherapy: a New Approach in Breast Cancer Treatment

No phase Interventional Female Breast Cancer Patients

For patients and families

In plain language

An automatic summary of structured registry data. It is an orientation aid, not a substitute for the official protocol or a physician assessment.

What is being studied
The protocol lists: UMAY - Video-immunotherapy game, Control - Plasebo Game.
Who it may be relevant to
Registry conditions: Female Breast Cancer Patients. Basic parameters: from 18 years · Female.
What needs checking
Age, condition and sex are only basic indicators. Prior treatment, laboratory values and other mandatory requirements appear in the eligibility criteria below.
Where it takes place
Turkey (Türkiye)
Next step
Save the trial, show it to the treating physician, and confirm current recruitment with the study center. Costs, documents and travel →

Overview

Breast cancer is the most common type of cancer among women worldwide and in Türkiye and remains one of the leading causes of cancer-related mortality. The high mortality rate and the fact that the disease severely reduces patients' quality of life create an urgent need for the development of innovative therapeutic approaches. Cancer immunotherapy aims to inhibit tumor growth and spread by harnessing the immune system. The fact that the immune system interacts with the nervous system and the endocrine system reveals that the integrity of the body and mind is very important in strengthening the immune system against cancer. Within the scope of psychoneuroimmunology, studies such as meditation, breathing therapy, hypnosis, and yoga have an indirect effect on the immune system by reducing the stress level of the person and improving the psychology, while techniques such as guided imagery can play a direct role in regulating the immune system. It has been shown that guided imagery studies, which can create unexpected effects thanks to the inability of the human mind to distinguish between imagination and reality, can increase the activity of immune cells with anti-tumoral activity in cancer patients and even reduce patient mortality. In addition to the cytotoxic activities of immune system cells, imagery can also have an effect on the regulation of tissue migration. Therefore, guided imagery studies in breast cancer patients can contribute both to immune system regulation and to increase lymphocyte migration to the tumor tissue of patients if they are applied effectively and long-term enough. In guided imagery studies, it is thought that the effectiveness is limited by the stress experienced by the patients/subjects during the effort of practicing imagery. In addition, imagery vividness also plays a decisive role in the effectiveness. In this study, the investigators developed a video game in which immune cells fight breast cancer cells, and through this video game, patients will be able to easily, actively, and vividly visualize their immune cells destroying the cancer. In the meantime, instead of being stressed, the patients will be playing games and having fun with imagery. Thus, the investigators developed a unique guided imagery complementary therapy called video-immunotherapy in the treatment of breast cancer. It is predicted that the immune system of the person playing the video game would be stimulated to exert an anti-tumoral effect. In this study, breast cancer patients will play the video immunotherapy or a control placebo video game in addition to their current treatment (neoadjuvant chemotherapy). The effect of the video immunotherapy on the course of the disease, physiological symptoms, and psychological well-being of the patients will be measured, and the effect of the game on the immune cells of the patients will be analyzed in detail.

Interventions

  • Behavioral UMAY - Video-immunotherapy game
    "UMAY" video-immunotherapy about immune cells fighting breast cancer - participants will play the UMAY video game offered as a mobile phone app at home for at least 20 minutes at least 4 days a week.
  • Behavioral Control - Plasebo Game
    participants will play the placebo video game as a mobile phone app at home for at least 20 minutes at least 4 days a week.

Primary outcome measures

  • Change from baseline in Depression Anxiety Stress Scale (DASS-42) total score [Time frame: Experimental and control group patients will answer questionnaires to monitor their psychological status and physiological symptoms 3 times in total: baseline (month 0), during the treatment (month 3) and at the end of treatment (month 5-6).]
  • Change from baseline in Edmonton Symptom Assessment System-revised (ESAS-r) total symptom score [Time frame: Baseline (Month 0), during treatment (Month 3), and end of treatment (Month 5-6)]
  • Change from baseline in frequency of immune cell subsets in peripheral blood and tumor tissue [Time frame: Peripheral blood: Baseline (Month 0) and end of treatment (Month 5-6) Tumor tissue: End of treatment (Month 5-6)]
  • Change from baseline in activation marker expression on immune cell subsets [Time frame: Peripheral blood: Baseline (Month 0) and end of treatment (Month 5-6) Tumor tissue: End of treatment (Month 5-6)]
  • Change from baseline in tumor size measured by ultrasound and mammography for the assessment of the effects on disease progression [Time frame: Baseline (Month 0), mid-treatment (Month 3), and end of treatment (Month 5-6)]

Eligibility criteria

Inclusion criteria

  • having locally advanced breast cancer
  • To be over 18 years old
  • Volunteering to participate in the study
  • ECOG performance score of 0-1
  • To be able to communicate in Turkish
  • Obtaining written informed consent for participation in the study

Exclusion criteria

  • History of epilepsy and similar seizures
  • History of cognitive impairment such as dementia, Alzheimer's disease
  • Major depression or suicidal tendencies
  • Traumatic brain injury
  • Lack of sight, hearing or use of hands
  • Previous history of cancer other than breast cancer
  • Chronic use of immunosuppressive drugs (e.g. steroids)
  • Active immunodeficiency
  • Having any disability to play video games

Criteria are shown verbatim from the registry (in English). Final eligibility is always assessed by the study center.

Healthy volunteers: No

Study design

Allocation
Randomized
Model
Parallel assignment
Masking
Double blind
Primary purpose
Supportive care

Study locations

Turkey (Türkiye) · 3 centers
  • Dokuz Eylul University Hospital — Izmir
  • Akdeniz University Hospital — Antalya
  • Antalya Training and Research Hospital — Antalya

Identifiers

NCT: NCT07357207 · iBG-2022-017 · 121C245

Primary sources (government registries)

View this study on ClinicalTrials.gov ↗