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Opiate Dependency RelapseNCT01955902

Using mHealth to Aid Opioid Addicts

An observational study of Opiate Dependency Relapse, run by Care Team Solutions at 1 site in United States.

Completed

Finished. The study has ended and is not enrolling. Results may be posted on the official record.

Official record
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Trial summary

The purpose of the proposed study is perform focus groups to identify and prioritize features of the SubAID application (APP). The SubAID APP is smartphone APP being created to support patients self-managing buprenorphine/naloxone (bup/nal) medication. Read more about this study

Who is it for?
Ages 21 years and older
Conditions the study is for
Opiate Dependency Relapse
How many people
11 participants
Where
1 siteUnited States
Study dates
Aug 2013to Oct 2013
Phase
Observational
Are there results?
None posted in the registry

Key requirements

Who can take part, as listed by the sponsor. Only the study team can confirm whether you are eligible, so take this list to your doctor.

  • Ages 21 years and older
  • All sexes
  • No healthy volunteers
  • Adult, Older adult

Study population: Community Sample

Who may be able to join

  • At least 21 years of age
  • Physician diagnosis of opioid dependence (OD)
  • Prescribed buprenorphine/naloxone (bup/nal) and acclimated to the medication
  • Able to speak and read English
  • Willing to provide written informed consent prior to study entry
  • Able to understand the study
  • Ownership of an Android or iPhone smartphone

Who cannot join

  • Having any concurrent medical or psychiatric condition that, in the investigator's opinion, may preclude participation in this study; or
  • Cognitive or other impairment (e.g., visual) that would interfere with completing a self-administered questionnaire and with participating in a group discussion.

Trial locations and contacts

1 site in 1 country.

United States1 site
  • Care Team Solutions

    Lexington, Kentucky, 40507

Other trials in United States

About this study

Official title: Using mHealth to Aid Opioid Medication Adherence Focus Groups

The purpose of the proposed study is perform focus groups to identify and prioritize features of the SubAID application (APP). The SubAID APP is smartphone APP being created to support patients self-managing buprenorphine/naloxone (bup/nal) medication. Many people have difficulty in managing bup/nal in the prescribed manner. Not taking medicines in their prescribed manner can cause negative health outcomes.

Focus group participants will be asked to elaborate on medication-taking patterns that work best for them, pitfalls associated with poor adherence and offer opinions upon what features/functions the SubAID APP should perform to be most helpful to them. The focus group is designed to remain open-ended and allow free discussion regarding each particular topic that the moderator will bring up.

Read the detailed description

Opioid dependence (OD) is a serious medical and social quandary impacting the lives of millions, including disparate demographic populations in the United States. Economic and societal costs of prescription opioid abuse in the United States alone are estimated at $56 billion while the number of drug poisoning deaths attributed to opioid analgesics has more than tripled since 1999. In 2008, opioid analgesics were involved in greater than 40% of all drug poisoning fatalities. Opiate-agonist pharmacotherapy utilizing buprenorphine/naloxone (bup/nal) is known to decrease illicit opiate use. However, poor medication management and misuse during self-managed opioid substitution therapy (OST) constrains efficacy, while aggrandizing relapse, hospitalizations and mortality. In an adherence study, OST patients that mismanaged their medication were >10 times more likely to relapse than compliant patients. [5] Thus, one of the most inescapable challenges confronted by health care professionals treating OD is assuring medications are taken as prescribed to inhibit relapse. Yet, the threats to successful medication mismanagement for substance use disorders are unique from those of traditional chronic diseases.

While the ultimate goal of substance abuse treatment is abstinence, opioid addiction is a chronic, relapsing medical condition. Opioid substitution therapy, incorporating methadone or bup/nal, represents conventional treatment options for opioid dependence. Methadone maintenance in adequate doses reduces cravings, prevents the onset of withdrawal, is not intoxicating or sedating, and does not interfere with normal activities of daily living. However, significant pitfalls denote methadone maintenance treatment. Methadone is a long-acting, full opioid agonist with known abuse and diversion potential and no upper boundary to the level of respiratory depression -- overdose can therefore be fatal. In addition, relapse rates for methadone maintenance range between 55-90% following treatment. Although an effective therapy, the high rates of relapse and diversion render methadone a less than ideal solution for many patients. Recently, the bup/nal formulation, commonly sold as Suboxone®, was designed to minimize abuse and diversion while retaining all positive aspects of methadone treatment. Bup/nal has proven correspondingly effective in treating OD as methadone, and more efficient in certain populations. Clinical studies have shown the beneficial effect of bup/nal treatment in reducing subsequent opioid use. Administered sublingually, naloxone undergoes extensive first-pass metabolism and has negligible bioavailability; thus, when used as prescribed, the combination drug (bup/nal) produces effects of buprenorphine alone. However, if injected, the naloxone will precipitate withdrawal in opioid dependent patients. Thus, bup/nal is intended to reduce the risk of illicit use by injection. An additional benefit of bup/nal OST is unsupervised use. Unlike methadone maintenance, which generally entails a daily clinic visit, bup/nal allows the patient increased freedom, typically requiring only one physician and pharmacy visit per month after a stabilization period. Given its lower abuse appeal, strong effectiveness, and clear ability to lower relapse rates, bup/nal represents a more suitable treatment option for OD, especially in still working individuals.

In spite of moves toward more unsupervised and self-managed OST with bup/nal, monitoring and promoting effective medication adherence is challenging for a number of reasons including diversion, lack of motivational support to avoid opioids, and low health literacy. Affording patients and their caregivers an interactive toolset to effectively monitor and promote medication management during OST therefore represents a major unmet need that this project will address. This research project will develop an interactive smartphone/tablet application (APP), named SubAID, designed to engage and support patients receiving bup/nal to promote and monitor adherence. In order to develop the most appropriate and effective adherence support content for the SubAID APP, we will solicit opinions in Focus Groups from OD subjects prescribed bup/nal to better understand the adherence complications and problems they encounter on a daily basis.

Keywords
Opioid dependence, Buprenorphine, Adherence, Substance use, Suboxone
Medical subject headings
Opioid-Related Disorders, Substance-Related Disorders

What participants receive

What participants receive. In a randomised study each person is assigned to one group by chance.

Study groups in NCT01955902
Study groupRoleWhat they receive
Opioid addictsOpioid addicts undergoing bup/nal maintenance therapy

What is being measured

The primary outcome is the main question the study is designed to answer.

  1. Attitudes, beliefs and perceptions

    Content analysis will be used to evaluate the information gathered during the focus groups. The analysis will be based on recall, notes taken by the co-facilitator, and transcripts from session recordings. The evaluation process will include the following: 1) generation of key words, phrases, and quotes concerning symptoms, concerns or fears about their ability to effectively manage maintenance medications, and 2) identification of additional, emergent themes in each of the SubAID features that would be helpful and relevant to the impact of managing maintenance therapy medications. To be considered credible, themes included in the final analysis will be features or concerns that were raised by more than one participant in a single group, and, ideally, by participants in more than one group.

    Measured: Up to 8 weeks

Timeline

From the start of the study to its completion; the mark is today. Estimated dates are the sponsor’s plan.

  1. First posted8 Oct 2013 (estimated)
  2. Study startAug 2013
  3. Primary completionOct 2013
  4. Study completionOct 2013

Resources

More details

For doctors and researchers: how the study is designed, who runs it, and its registry IDs.

Study design
Study type
Observational
Observational model
Cohort
Time perspective
Prospective
Enrolment
11 participants (actual)
IDs, dates and publications
ClinicalTrials.gov ID
NCT01955902
Sponsor's protocol ID
271201300015C
Status last verified
Nov 2013
First submitted
26 Sep 2013
Last updated
11 Nov 2013
Results posted
No
Data monitoring committee
No

Questions about this trial

What is this clinical trial studying?

An observational study of Opiate Dependency Relapse, run by Care Team Solutions at 1 site in United States.

The full registered description is in the About this study section and the official record.

Who may be eligible to take part?

The sponsor lists 7 inclusion and 2 exclusion criteria. Eligibility is decided by the study team after screening, so read the full criteria and contact a listed site.

Is this clinical trial currently recruiting?

The record says: finished, as of the sponsor's last update on 11 Nov 2013. Status can change between updates, so confirm with the study contact before making plans.

Where is the study taking place?

The record lists 1 site in United States. Whether a site is taking part right now should be confirmed with that site. See every site.

What are the possible benefits and risks?

They depend on the study and the treatment, and no study can promise a benefit. The study team explains the known risks during informed consent, before anyone joins; the record itself does not list them.

Are results available for this study?

The study is completed, but results are not available in the source record. That does not mean the treatment did or did not work.

How can a doctor refer a patient or contact the research team?

The record lists no contact. The official record names the sponsor, who can be asked directly. AzTrials does not enrol participants or take referrals.

What does the primary outcome measure?

Attitudes, beliefs and perceptions (time frame: Up to 8 weeks). It is what the study was designed to measure, not a finding.

Where can I read the original study information?
Does a listing mean the treatment is approved or proven to work?

No. A listing means the study is registered. It does not show that the treatment is safe, works, or is approved by a regulator.

How often is this information updated?

AzTrials copies changed records from ClinicalTrials.gov every night and reloads the whole registry every week. The sponsor last updated this record on 11 Nov 2013.

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