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Flexible Attention Sensory Training for Youth with Chronic Pain

Stanford University logo

Stanford University

Status

Completed

Conditions

Persistent Pain

Treatments

Behavioral: Sensory Training

Study type

Interventional

Funder types

Other

Identifiers

Details and patient eligibility

About

The purpose of this study is to determine the feasibility and acceptability of gamified sensory rehabilitation training technology for children with chronic musculoskeletal pain.

Full description

The TrainPain devices allows patients with chronic pain to perform sensory rehabilitation training at home, in a gamified format. The system uses a temporary tactile discrimination task, which directly engages inhibitory functions of the somatosensory cortex. In this way, the game trains the brain's sensory system to be more precise. The technology's dual-probe system allows sensory stimuli to be delivered to multiple body locations, which trains patients to flexibly shift their attention towards and away from pain according to dynamic game-directed goals. The sensory training reduces hypervigilance towards painful body regions and enables flexible attention shifting to engage with daily goals. Last, the TrainPain system captures and quantifies performance over time, providing a breadth of intricate and precise data, thus allowing the research team to assess outcomes and mechanisms of training effects. In preliminary studies with adults, TrainPain is shown to be highly engaging, and effective at reducing pain in adults with widespread musculoskeletal (MSK) pain. The current pilot study intends to establish, for the first time, the feasibility and acceptability of using the TrainPain system among youth with chronic MSK pain.

Enrollment

27 patients

Sex

All

Ages

10 to 17 years old

Volunteers

No Healthy Volunteers

Inclusion criteria

  • Diagnosis of musculoskeletal pain including chronic regional pain syndrome
  • English speaking

Exclusion criteria

  • Diagnosis of neurological conditions such as seizures, cerebral palsy, developmental delay
  • Severe affect disorders (e.g. severe depression/anxiety) from medical record review
  • Chronic skin disease or topical allergies that would be worsened by the use of sensor tape

Trial design

Primary purpose

Treatment

Allocation

N/A

Interventional model

Single Group Assignment

Masking

None (Open label)

27 participants in 1 patient group

Sensory Training
Experimental group
Description:
Daily protocol - gamified sensory training
Treatment:
Behavioral: Sensory Training

Trial contacts and locations

1

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Central trial contact

Laura Simons, PhD; Nicole Jehl, BS

Data sourced from clinicaltrials.gov

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