Pain Clinical Trial
Official title:
Virtual Reality for Symptoms Control in Palliative Care
The aim of this study is to evaluate how Virtual Reality (VR) can be used to control symptoms
and improve the quality of life in palliative care. The interventional prospective case
control study is planned to contain five phases including two control groups. The following
describes only phase one to three.
In the pilot phase patients get a one-time application of the VR-Technology. After that, two
control groups will be recruited from patients with 1. mamma carcinoma and the indication of
(neo-) adjuvant radiotherapy and 2. before a colonoscopy-treatment. Both groups receive the
VR application before treatment (radiotherapy/colonoscopy).
This first part proofs the application of Virtual Reality on patients in palliative care with
the aim to control symptoms and reduce pain and anxiety.
The clinical study hypothesis bases on the assumption that VR reduces pain and anxiety and
may have a positive influence on their quality of life.
Pilot phase:
After the enrolment and consent of participation the patient receives a questionnaire
consisting of different independent assessments. The visual analogue scale with values from 1
to 10 quantifies subjective pain. A functional pain questionnaire (Pain-Out) is developed to
assess the pain in between the last seven days, the associated limitations, the actions and
side effects of combined pain therapy.
To measure the generic health-related quality of life the patient is asked to answer the
EuroQoL Group 5-Dimension 5-Level Self Report Questionnaire (EQ-5D-5L).
A Virtual Reality application is offered immediately after the questionnaire has been
completed. Following the application of VR the patient will receive VAS and functional pain
questionnaires again to assess the change from baseline.
Control phase:
The following control phase is to review the effectiveness of VR application on the basis of
two different control groups. In a randomized setting 30 patients with mamma carcinoma
receive an application of VR before their radiotherapy. The second control group consists of
40 patients with an individual indication of a colonoscopy.
Instead of pain by VAS and QoL in the pilot phase each patient receives now the Hospital
Anxiety and Depression Scale (HADS) before and after the application. The Functional Pain
Questionnaire remains with the control group of patients with mamma carcinoma.
;
| Status | Clinical Trial | Phase | |
|---|---|---|---|
| Active, not recruiting |
NCT05559255 -
Changes in Pain, Spasticity, and Quality of Life After Use of Counterstrain Treatment in Individuals With SCI
|
N/A | |
| Completed |
NCT04748367 -
Leveraging on Immersive Virtual Reality to Reduce Pain and Anxiety in Children During Immunization in Primary Care
|
N/A | |
| Terminated |
NCT04356352 -
Lidocaine, Esmolol, or Placebo to Relieve IV Propofol Pain
|
Phase 2/Phase 3 | |
| Completed |
NCT05057988 -
Virtual Empowered Relief for Chronic Pain
|
N/A | |
| Completed |
NCT04466111 -
Observational, Post Market Study in Treating Chronic Upper Extremity Limb Pain
|
||
| Recruiting |
NCT06206252 -
Can Medical Cannabis Affect Opioid Use?
|
||
| Completed |
NCT05868122 -
A Study to Evaluate a Fixed Combination of Acetaminophen/Naproxen Sodium in Acute Postoperative Pain Following Bunionectomy
|
Phase 3 | |
| Active, not recruiting |
NCT05006976 -
A Naturalistic Trial of Nudging Clinicians in the Norwegian Sickness Absence Clinic. The NSAC Nudge Study
|
N/A | |
| Completed |
NCT03273114 -
Cognitive Functional Therapy (CFT) Compared With Core Training Exercise and Manual Therapy (CORE-MT) in Patients With Chronic Low Back Pain
|
N/A | |
| Enrolling by invitation |
NCT06087432 -
Is PNF Application Effective on Temporomandibular Dysfunction
|
N/A | |
| Completed |
NCT05508594 -
Efficacy and Pharmacokinetic-Pharmacodynamic Relationship of Intranasally Administered Sufentanil, Ketamine, and CT001
|
Phase 2/Phase 3 | |
| Recruiting |
NCT03646955 -
Partial Breast Versus no Irradiation for Women With Early Breast Cancer
|
N/A | |
| Active, not recruiting |
NCT03472300 -
Prevalence of Self-disclosed Knee Trouble and Use of Treatments Among Elderly Individuals
|
||
| Completed |
NCT03678168 -
A Comparison Between Conventional Throat Packs and Pharyngeal Placement of Tampons in Rhinology Surgeries
|
N/A | |
| Completed |
NCT03931772 -
Online Automated Self-Hypnosis Program
|
N/A | |
| Completed |
NCT03286543 -
Electrical Stimulation for the Treatment of Pain Following Total Knee Arthroplasty Using the SPRINT Beta System
|
N/A | |
| Completed |
NCT02913027 -
Can We Improve the Comfort of Pelvic Exams?
|
N/A | |
| Terminated |
NCT02181387 -
Acetaminophen Use in Labor - Does Use of Acetaminophen Reduce Neuraxial Analgesic Drug Requirement During Labor?
|
Phase 4 | |
| Recruiting |
NCT06032559 -
Implementation and Effectiveness of Mindfulness Oriented Recovery Enhancement as an Adjunct to Methadone Treatment
|
Phase 3 | |
| Active, not recruiting |
NCT03613155 -
Assessment of Anxiety in Patients Treated by SMUR Toulouse and Receiving MEOPA as Part of Their Care
|