ClinicalTrials.Veeva

Menu

Boost Study 31380 (mHealth)

N

NXTech

Status and phase

Completed
Phase 1

Conditions

Addiction

Treatments

Device: mHealth

Study type

Interventional

Funder types

Industry
NIH

Identifiers

NCT05757453
1R43DA051270 (U.S. NIH Grant/Contract)
NX-31380

Details and patient eligibility

About

The purpose of this research is to examine the potential for a new software-based behavioral support approach, for individuals with opioid use disorder, as an addition to usual care.

Full description

The purpose of this study is to examine the potential for a novel computer-based approach to mitigate the symptoms of opioid use disorder as part of a comprehensive treatment program. The study is designed as a single-arm field-test of cognitive training for individuals under supervised medical treatment for opioid use disorder. A custom and proprietary smartphone package (mHealth platform) comprises the intervention available to enrolled subjects for interaction over the study period. Commercial mobile devices serve as information presentation and data recording instruments. Additional outcome measures incorporate subject-reported data.

Enrollment

43 patients

Sex

All

Ages

18 to 65 years old

Volunteers

No Healthy Volunteers

Inclusion criteria

  • Age 18-65 years
  • Diagnosis of opioid use disorder
  • Experiencing symptoms multiple times per week
  • Familiar with smartphone usage

Exclusion criteria

  • None specified

Trial design

Primary purpose

Treatment

Allocation

N/A

Interventional model

Single Group Assignment

Masking

None (Open label)

43 participants in 1 patient group

Experimental
Experimental group
Description:
mHealth group
Treatment:
Device: mHealth

Trial documents
2

Trial contacts and locations

1

Loading...

Data sourced from clinicaltrials.gov

Clinical trials

Find clinical trialsTrials by location
© Copyright 2026 Veeva Systems