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Distraction Techniques for Blood Cancers

N/A
Waitlist Available
Research Sponsored by Thomas Jefferson University
Eligibility Criteria Checklist
Specific guidelines that determine who can or cannot participate in a clinical trial
Must have
Over 18 years of age
Be older than 18 years old
Timeline
Screening 3 weeks
Treatment Varies
Follow Up within 10 minutes post-procedure
Awards & highlights

Study Summary

This trial is testing if distraction techniques during a bone marrow biopsy/aspiration can reduce distress, pain and improve satisfaction. Interventions include VR and nature-themed decals/music.

Who is the study for?
This trial is for adults over 18 who've had a bone marrow biopsy/aspiration at Jefferson's outpatient oncology office in the last two years and are due for another during the study. They must understand and agree to all study procedures.Check my eligibility
What is being tested?
The study tests if distraction techniques like virtual reality meditation or room changes with music can reduce distress, pain, and improve satisfaction compared to standard care during BMBA procedures.See study design
What are the potential side effects?
Since this trial involves non-invasive interventions such as VR meditation and environmental adjustments, side effects may include discomfort from wearing a VR headset or personal reactions to environmental changes.

Eligibility Criteria

Inclusion Criteria

You may be eligible if you check “Yes” for the criteria below
Select...
I am over 18 years old.

Timeline

Screening ~ 3 weeks
Treatment ~ Varies
Follow Up ~within 10 minutes post-procedure
This trial's timeline: 3 weeks for screening, Varies for treatment, and within 10 minutes post-procedure for reporting.

Treatment Details

Study Objectives

Outcome measures can provide a clearer picture of what you can expect from a treatment.
Primary outcome measures
Distress score
Secondary outcome measures
Pain intensity
Patient satisfaction

Trial Design

4Treatment groups
Experimental Treatment
Active Control
Group I: Intervention 2: Environmental changesExperimental Treatment1 Intervention
Group II: Intervention 1: Virtual realityExperimental Treatment1 Intervention
Group III: Control 1Active Control1 Intervention
Standard of care without change, in parallel with intervention 1: Virtual reality.
Group IV: Control 2Active Control1 Intervention
Standard of care without change, in parallel with intervention 2: Environmental changes.

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Who is running the clinical trial?

Thomas Jefferson UniversityLead Sponsor
445 Previous Clinical Trials
145,654 Total Patients Enrolled
3 Trials studying Lymphoma
179 Patients Enrolled for Lymphoma
Daisy FoundationOTHER
3 Previous Clinical Trials
212 Total Patients Enrolled

Frequently Asked Questions

These questions and answers are submitted by anonymous patients, and have not been verified by our internal team.

Is there still availability for volunteers in this research project?

"According to clinicaltrials.gov, this specific trial is no longer recruiting patients - the last update was made on January 9th 2023. Despite that, there are an abundance of other trials actively searching for volunteers right now; 3610 in total."

Answered by AI
~26 spots leftby Apr 2025