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Safely Disposing of Surplus Prescription Opioids (DISPOSE)

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Johns Hopkins University

Status

Completed

Conditions

Opioid Use

Treatments

Behavioral: Informational Sheet
Behavioral: DisposeRx Drug Disposal kit

Study type

Interventional

Funder types

Other

Identifiers

NCT03855241
IRB00205030

Details and patient eligibility

About

This study evaluates two interventions intended to increase the safe disposal of leftover prescription opioids, compared to no intervention. Participants will receive an informational sheet describing how to safely dispose of leftover prescription opioids, an informational sheet with a drug disposal kit, or no intervention. Participants will be randomized by day for pragmatic reasons.

Full description

Many persons who receive a prescription for opioids report having leftover opioids once the prescription is finished. Leftover prescription opioids serve as a reservoir of products for misuse, given 90% of people who misuse prescription opioids report obtaining the opioids from a friend, family member, or a legitimate prescription. The best way to increase the rate of safe disposal of leftover opioids is unclear. The present study will generate evidence comparing how well a drug disposal system compares with providing an informational handout on properly disposing of leftover prescription opioids. Participants will be randomized by day to one of two disposal interventions or no disposal intervention. Disposal interventions include a drug disposal kit or an informational sheet describing how to safely dispose of leftover prescription opioids. Storage and disposal characteristics for leftover prescription opioids will be measured using standardized telephone calls with participants at 3 weeks after filling the opioid prescription. If therapy is not concluded at 3 weeks or participants are not available, then a second standardized telephone call with participants will take place at 6 weeks after filling the opioid prescription.

Enrollment

499 patients

Sex

All

Ages

18+ years old

Volunteers

No Healthy Volunteers

Inclusion criteria

  • Adult participants (age ≥ 18 years) who pick up a prescription for themselves or a family member at a Johns Hopkins pharmacy
  • English speaking
  • Residential address and phone number in the United States
  • Filling a new prescription consisting of an immediate release opioid medication (i.e., immediate release morphine, oxycodone, hydromorphone, hydrocodone, tramadol; alone or in combination with acetaminophen) with ≤ 7 days' supply

Exclusion criteria

  • Age < 18 years
  • Non-English speaking
  • Residential address and/or phone number outside the United States
  • Opioid medication listed in participant's active medication list prior to prescription fill
  • Filling any prescription consisting of any opioid with 8 or more days' supply
  • Filling any prescription consisting of any extended-release / long-acting opioid medication (i.e., extended-release morphine, oxymorphone, oxycodone, hydromorphone, fentanyl, methadone, buprenorphine)
  • Filling an opioid prescription indicated for cough or shortness of breath

Trial design

Primary purpose

Other

Allocation

Randomized

Interventional model

Parallel Assignment

Masking

Single Blind

499 participants in 3 patient groups

Informational Sheet
Active Comparator group
Description:
Persons picking up an opioid prescription will receive an informational sheet that describes how to properly dispose of leftover opioid medications
Treatment:
Behavioral: Informational Sheet
Drug Disposal Kit
Active Comparator group
Description:
Persons picking up an opioid prescription will receive a drug disposal kit (DisposeRx Drug Disposal kit) and instructions on how to use it
Treatment:
Behavioral: DisposeRx Drug Disposal kit
Behavioral: Informational Sheet
No intervention
No Intervention group
Description:
Persons picking up an opioid prescription will receive no additional information or materials on disposal.

Trial documents
1

Trial contacts and locations

1

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Data sourced from clinicaltrials.gov

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