Immersive Technology Headsets to Reduce Procedural Pain and Anxiety: Feasibility and Effects in Cutaneous Leishmaniasis Patients in Pakistan

Trial statusNot yet recruiting
Trial phaseNot applicable
Trial typeInterventional
Biological sexAll
Age5-99
SponsorStanford University

About this trial

The goal of this clinical trial is to learn whether immersive technology (virtual reality) headsets can reduce procedural pain and anxiety during diagnosis, intralesional and intramuscular injections, and wound/dressing care in pediatric patients 5 years of age and older and adult patients with cutaneous leishmaniasis receiving treatment at the MSF clinic in Peshawar, Khyber Pakhtunkhwa, Pakistan.

Eligibility criteria

This trial does not accept healthy volunteers

Qualifiers

Pediatric cutaneous leishmaniasis patients

Receiving cutaneous leishmaniasis care (diagnosis, treatment, and/or wound/lesion management) at the MSF cutaneous leishmaniasis facility in Peshawar

Disqualifiers

Legal guardian not present to obtain consent

Child with a significant neurological condition, or major developmental disability

A history of severe motion sickness

A history of seizures cause by flashing light

Trial design

Design model

Single group

Treatments tested in this trial

  • Virtual Reality

    Behavioral

    Participants interact with virtual reality games designed for procedural distraction while receiving medical treatment. Following treatment completion, participants undergo brief surveys and a semi-structured interview.

Treatment groups

15 Participants
are divided into 1 treatment group
Group A: Cutaneous leishmaniasis (CL) patientExperimental treatment 1 intervention

Trial outcomes

Primary outcomes

1

Participant feasibility and acceptability regarding immersive technology

Qualitative evaluation of participant attitudes, perceptions, and user experience with immersive technology headsets collected via semi-structured focus group interviews. Feedback will be categorized into core thematic domains including ease of use, comfort, and willingness to use in future care.

Time frame
Immediately after intervention

Secondary outcomes

Other outcomes

Locations

This trial has no locations.

Sponsors and contacts

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This trial is not recruiting at the moment. You can still explore other options: