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Mindfulness-based Virtual Reality Intervention

Efficacy of Mindfulness-based Virtual Reality Intervention on the Symptoms Associated With Hematologic Neoplasms Patients During Chemotherapy

Status
UNKNOWN
Phases
NA
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT05602051
Enrollment
110
Registered
2022-11-01
Start date
2021-11-01
Completion date
2022-12-01
Last updated
2022-11-01

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Hematologic Neoplasms

Brief summary

Through virtual reality technology and mindfulness therapy, we can intervene the patients with Hematologic Neoplasms during chemotherapy, hoping to improve their symptoms and self-efficacy.

Detailed description

In recent years, the intervention method of giving mindfulness has achieved good results in the management of symptoms related to cancer patients, but the compliance of patients with conventional mindfulness intervention is low. The virtual reality intervention based on mindfulness can effectively mobilize the enthusiasm of patients to participate in research and the compliance of mindfulness training. We aim to combine virtual reality with mindfulness intervention to intervene patients with hematologic neoplasms during chemotherapy, To improve their symptoms.

Interventions

mindfulness combined with virtual reality

Sponsors

Nanjing University of Traditional Chinese Medicine
Lead SponsorOTHER

Study design

Allocation
RANDOMIZED
Intervention model
PARALLEL
Primary purpose
SUPPORTIVE_CARE
Masking
SINGLE (Outcomes Assessor)

Eligibility

Sex/Gender
ALL
Age
18 Years to 85 Years
Healthy volunteers
No

Inclusion criteria

* Clinical diagnosis of Hematologic Neoplasms(leukemia, lymphoma or multiple myeloma) and receiving chemotherapy * Hospitalized for more than 4 weeks * Have normal communication ability, clear consciousness, and willing to participate in this study

Exclusion criteria

* People are cognitive dysfunction and audio-visual dysfunction * Have mental problems or have reported mental disorders

Design outcomes

Primary

MeasureTime frameDescription
MDASI-Cup to 7 weeksSymptom burden was assessed using the Chinese version of the M. D. Anderson Symptom Inventory (MDASI-C),39 which is a self-report scale consisting of two domains. The first domain is named core symptom severity items and has 13 symptoms. Each symptom is rated on an 11-point scale (0-10) to indicate the presence and severity of the symptom, with 0 indicating not present and 10 indicating as bad as you can imagine. Each symptom is rated based on the severity of the symptom, at its worst, in the last 24 h. The second domain is named six symptoms interference items and includes ratings of how much symptoms interfered with different aspects of the survivor's life in the last 24 h. The interference items are also rated on a scale of 0-10, with 0 indicating did not interfere and 10 indicating interfered completely. A score of 0-3 indicated a mild level, 4-6 indicated a moderate level, and 7-10 indicated a severe level of symptom severity or interference.
Hospital Anxiety and Depression Scale (HADS)up to 7 weeksThe hospital anxiety and depression scale The HADS was compiled by Zigmond AS Which was used to detect states of depression and anxiety in the setting of an hospital medical outpatient clinic . It is a 14-question instrument, with each question being scored between 0 (no impairment) and 3 (severe impairment), with a maximum score of 21 for anxiety or depression.

Secondary

MeasureTime frameDescription
the self-management efficacy scale (C-SUPPH)up to 7 weeksthe self-management efficacy scale (C-SUPPH),The C-SUPPH scale consisted of 28 items in three dimensions: self-decompression, self-decision-making, and positive attitude, with each item scoring 1-5 points and a total score of 28-140 points. The higher the total score is, the higher the self-efficacy is.

Countries

China

Contacts

Primary ContactYuan Wu
1528046998@qq.com18895611517

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 4, 2026