Clinical trial · Interventional
Effect of Virtual Reality on Pain and Anxiety During Chemotherapy Session in Breast Cancer Patients
NCT07292727CI-TRIAL-00099233not yet recruitingN/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)
This study will be conducted to determine the effect of virtual reality exercise on pain and anxiety in breast cancer patients during chemotherapy treatment
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 Cancer | Malignant Breast Neoplasm | CURATED_EXACT | 0.92 |
Interventions
Interventions (2)
| Intervention | Type | Mapped drug | Match |
|---|---|---|---|
| traditional care | Other | — | UNRESOLVED |
| Virtual reality | Other | — | UNRESOLVED |
Design
Arms and outcomes
Arms (2)
- type
- ACTIVE_COMPARATOR
- label
- Traditional care group
- description
- This group includes patients suffering from pain and anxiety. Patients will receive their traditional care at every chemotherapy session
- interventionNames
- Other: traditional care
- type
- EXPERIMENTAL
- label
- Virtual reality group
- description
- This group includes patients suffered from pain and anxiety. The patients received their traditional care in addition to a fully immersive Head-Mounted Display virtual reality.
- interventionNames
- Other: traditional care
- Other: Virtual reality
Primary outcomes (2)
- measure
- Assessment of pain intensity
Eligibility
Eligibility (as posted)
- Sex
- Female
- Minimum age
- 30 Years
- Maximum age
- 55 Years
Show eligibility criteria text
Inclusion Criteria: * Patients who are diagnosed with breast cancer. * Patients who suffered from pain. * Patient who suffered from anxiety. * Patients who received chemo since 1cycle (session). * Patients who received the same type of chemotherapy. * Patients who are not suffer from anxiety disorders before chemotherapy. * Patient who received chemotherapy for the first time in their treatment. Exclusion Criteria: The potential participants will be excluded if they have one of the following criteria: * injuries to the face or head * Hand Injuries. * Cognitive impairment * A history of severe motion sickness * Mental health problems. * Visual and auditory problems. * Radiotherapy * A history of skull structure or cervical spine abnormalities that may complicate the use of VR devices. * A history of epilepsy, seizures, vertigo.
References
Publications (0)
Data not yet available
No reference posted for this study.