Opioid Use DisorderRESTOREbNCT05591703
Clinical Outcomes Following Transcutaneous Auricular Neurostimulation to Improve Relapse Prevention: A Long-term Follow-up Study
An observational study of Opioid Use Disorder and Relapse, run by Spark Biomedical, Inc. at 3 sites in United States.
Trial summary
This is a prospective, observational, longitudinal study to assess clinical outcomes in the 12-months following participants' exit from protocol SBM-OWP-03, Delivering Transcutaneous Auricular Neurostimulation to Improve Relapse Prevention in Opioid Use Disorder (RESTORE; ClinicalTrials.gov Identifier: NCT05053503). Read more about this study
- Who is it for?
- Ages 18 to 65 years
- Conditions the study is for
- Opioid Use Disorder, Relapse
- What is being tested?
- Clinical Outcomes and Questionnaires
- Type of treatment
- Lifestyle or therapy programme
- How many people
- 32 participants
- Where
- 3 sitesUnited States
- Study dates
- 21 Nov 2022to 31 Jan 2025
- 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 18 to 65 years
- All sexes
- No healthy volunteers
- Adult, Older adult
Study population: Participants with a history of dependence on prescription or non-prescription opioids
Who may be able to join
- Consented participant for protocol SBM-OWP-03, Delivering Transcutaneous Auricular Neurostimulation to Improve Relapse Prevention in Opioid Use Disorder (RESTORE)
- Participant is English proficient
- Participant is able to provide informed consent and function at an intellectual level sufficient for study requirements
Who cannot join
- Participant is unable to reliably receive and respond to assessments via email or telephone
- Participant has any other significant disease or disorder which, in the opinion of the Investigator, may either put the participants at risk because of participation in the trial, or may influence the result of the trial, or the participant's ability to participate in the trial
Trial locations and contacts
3 sites in 1 country.
United States3 sites
Hazelden Betty Ford Foundation
Center City, Minnesota, 55012
Hazelden Betty Ford Foundation
Plymouth, Minnesota, 55441
Betty Ford Foundation
Rancho Mirage, California, 92270
About this study
This is a prospective, observational, longitudinal study to assess clinical outcomes in the 12-months following participants' exit from protocol SBM-OWP-03, Delivering Transcutaneous Auricular Neurostimulation to Improve Relapse Prevention in Opioid Use Disorder (RESTORE; ClinicalTrials.gov Identifier: NCT05053503). Clinical outcome scores will be collected at study exit from protocol SBM-OWP-03, 1 month, 3 months, 6 months, 9 months, and 12 months after study exit from protocol SBM-OWP-03.
- Conditions
- Opioid Use Disorder, Relapse
- Being tested
- Clinical Outcomes and Questionnaires
- Keywords
- relapse prevention
- Medical subject headings
- Opioid-Related Disorders, Recurrence
What participants receive
What participants receive. In a randomised study each person is assigned to one group by chance.
Clinical Outcomes and QuestionnairesBehavioural
Clinical patient-reported outcomes will be administered remotely at specified timepoints. No treatment or intervention will be administered in this protocol.
| Study group | Role | What they receive |
|---|---|---|
| Participants randomized to receive tAN therapy in SBM-OWP-03 Phase II | Not described Receives: Behavioral: Clinical Outcomes and Questionnaires | |
| Participants not randomized to receive tAN therapy in SBM-OWP-03 Phase II | Not described Receives: Behavioral: Clinical Outcomes and Questionnaires |
What is being measured
The primary outcome is the main question the study is designed to answer.
Proportion of participants in Phase II with a relapse event
Measured: 12 months (total duration of trial)
Secondary outcomes (9)
Proportion of participants in either Phase I or Phase II with a relapse event
Comparison of the proportion of participants in either Phase I or Phase II with a relapse event over the 12-month follow-up period
Measured: 12 months (total duration of trial)
Mean change in recovery capital measured by Brief Assessment of Recovery Capital (BARC-10)
The BARC-10 is a short,10-item measure that examines recovery capital globally. Items were selected from the ARC for the BARC-10 using item response theory. The BARC-10 measures a unidimensional (i.e., global) construct of recovery capital across all the original 10 domains of the ARC. On average, it takes 2-5 minutes to complete. Scores range from 6-60. Individuals who have a recovery capital score of 47 or higher are likely to reach or sustain a year or longer of recovery from substance use disorder.
Measured: Baseline to Study Completion (12 months)
Mean change in opioid craving measured by the Opioid Craving Scale (OCS)
Participants are asked to answer the following three questions with responses ranging from 0-10, where 0=Not at all and 10=Extremely. Total possible score ranges from 0-30 with greater scores indicating higher opioid craving: (1) How much do you currently crave opiates? (2) In the past week, please rate how strong your desire to use opiates has been when something in the environment has reminded you of opiates (example: seeing a medication bottle, using the Internet, visiting a doctor's office, going to a place where you used to buy drugs)? (3) Please imagine yourself in the environment in which you previously used opiates (examples: a party, a hangout, a particular room where you live). If you were in this environment today and if it were the time of day that you typically used opiates, what is the likelihood that you would use opiates today?
Measured: Baseline to Study Completion (12 months)
Mean change in protracted withdrawal symptoms measured by the Short Opiate Withdrawal Scale-Gossop (SOWS-Gossop)
The SOWS-Gossop is an appropriate, precise, and sensitive measure to evaluate the symptoms of acute opioid withdrawal in research or clinical settings. The scale was derived from the original 32-item Opiate Withdrawal Scale to reduce redundancy while providing an equally sensitive measure of opioid withdrawal symptom severity appropriate for research and clinical practice. The assessment is a self-administered test used for the assessment of opiate withdrawal symptoms. The scale contains ten items: yawning, muscular tension, runny eyes, muscle twitching, pains, and aches, feeling of coldness, stomach cramps, insomnia, heart pounding, and feeling sick, making it easy and rapid to administer. The tool has a 4-point rating scale: 0 for 'none,' 1 for 'mild,' 2 for 'moderate,' and 3 for 'severe', with scores ranging from 0 to 30.
Measured: Baseline to Study Completion (12 months)
Mean change in depression symptoms across time measured by Patient Health Questionnaire (PHQ-9)
The PHQ-9 is a validated tool in mental health and considered a powerful tool to assist clinicians with diagnosing depression and monitoring treatment response. The relationship between opioid use and depression is bidirectional. The PHQ-9 is a nine-item depression scale and is based directly on the nine diagnostic criteria for major depressive disorder in the DSM-IV. Each of the nine items is rated on a 0 (not at all) to 3 (nearly every day) scale. A total score is calculated by summing the nine items. Scores range from 0 to 27 and higher scores indicate a higher degree of depression.
Measured: Baseline to Study Completion (12 months)
Mean change in anxiety across time measured by Generalized Anxiety Disorder (GAD-7)
The GAD-7 is a valid and efficient tool for screening for GAD and assessing its severity in clinical practice and research. The questionnaire consists of 7 questions in which participants are asked to rate each item on a 0 (not at all) to 3 (nearly every day). GAD-7 total score for the seven items ranges from 0 to 21 where 0-4 represents minimal anxiety, 5-9 represents mild anxiety, 10-14 represents moderate anxiety and 15-21 represent severe anxiety.
Measured: Baseline to Study Completion (12 months)
Mean change in PTSD symptoms across time measured by the PTSD Checklist for DSM-5 (PCL-5)
Symptoms of post-traumatic stress disorder (PTSD) and opiate dependency may overlap, to which, opioid withdrawal symptoms may emulate PTSD hyperactive startle response. This is indicative a common physiological mechanism. The PCL-5 scale is the gold standard in PTSD assessment. It consisted of a 20-item self-report measurement that is capable of measuring symptom change during and after treatment. Additionally, the scale can provide a provisional PTSD diagnosis. Each of the 20 items is rated on a 0 (not at all) to 4 (extremely) scale. A total symptom severity score is calculated by summing the 20 items. Scores range from 0 and 80 and higher scores indicating a higher degree of PTSD symptomology. Evidence suggests that a10 to 20-point reduction in score represents a clinically significant change in PTSD symptoms.
Measured: Baseline to Study Completion (12 months)
Mean change in Quality of Life across time measured by World Health Organization Quality of Life(WHOQOL-BREF) domain scores
The WHOQOL-BREF is a shorter version of the original assessment tool and is commonly used in clinical trials with participants undergoing substance use disorder intervention. The WHOQOL-BREF is comprised of 26-items and assesses the participant's quality of life across specific domains: physical health, psychological health, social relationships, and environment.24 In addition, there are 2 items that measure overall quality of life and general health. Participants rate how much they have experienced each item in the preceding two weeks on a 5-point Likert scale ranging from 1 (not at all) to 5 (completely). Domain scores are scaled in a positive direction with higher scores denoting higher quality of life. The mean score of items within each domain is used to calculate the domain score. Raw domain scores will be converted to a 0 to 100 scale.
Measured: Baseline to Study Completion (12 months)
Mean change in Commitment to Sobriety Scale (CSS-5)
Ratings of participant-perceived level of motivation and dedication to achieving initial and maintaining on-going sobriety for substance use will be measured using the 5-item Commitment to Sobriety Scale (CSS-5). Each statement is rated on a 6-point Likert scale, ranging from 1 (strongly disagree) to 6 (strongly agree). Example items include: "Staying sober is the most important thing in my life" and "I will do whatever it takes to recover from my addiction." Following the completion of the CSS-5, participants will be asked to reflect and rate level of confidence on their commitment to abstinence for the next 30 days using a 10-point scale, from 1 (not at all confident) to 10, (very confident).
Measured: Baseline to Study Completion (12 months)
Timeline
From the start of the study to its completion; the mark is today. Estimated dates are the sponsor’s plan.
- First posted24 Oct 2022
- Study start21 Nov 2022
- Primary completion31 Jan 2025
- Study completion31 Jan 2025
Resources
- Official record on ClinicalTrials.govThe registry entry this page is built from, with its full change history.
- Other trials for Opioid Use DisorderStudies of the same condition, open and under way.
- What the trial phases meanHow a treatment moves from first tests in people to approval.
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
- Case only
- Time perspective
- Prospective
- Enrolment
- 32 participants (actual)
Sponsor and investigators
- Lead sponsor
- Spark Biomedical, Inc.
- Sponsor type
- Industry (pharma, biotech, devices)
- Collaborators
- Hazelden Betty Ford Foundation
- Responsible party
- Sponsor
IDs, dates and publications
- ClinicalTrials.gov ID
- NCT05591703
- Sponsor's protocol ID
- SBM-OWP-03b
- Acronym
- RESTOREb
- Status last verified
- Apr 2025
- First submitted
- 19 Oct 2022
- Last updated
- 9 Apr 2025
- Results posted
- No
- Data monitoring committee
- No
- FDA-regulated drug
- No
- FDA-regulated device
- No
- Individual data sharing
- No
Study at a glance
From the registry record, last updated by the sponsor on 9 Apr 2025. Recruitment status is as the sponsor reported it: confirm with the study team.
- Official title
- Clinical Outcomes Following Transcutaneous Auricular Neurostimulation to Improve Relapse Prevention: A Long-term Follow-up Study
- ClinicalTrials.gov ID
- NCT05591703
- Acronym / sponsor ID
- RESTOREb / SBM-OWP-03b
- Conditions
- Opioid Use Disorder, Relapse
- Keywords
- relapse prevention
- Study type
- Observational
- Recruitment status
- Completed
- Enrolment
- 32 participants (actual)
- Lead sponsor
- Spark Biomedical, Inc.Industry (pharma, biotech, devices)
- Collaborators
- Hazelden Betty Ford Foundation
- Study start
- 21 Nov 2022 (actual)
- Primary completion
- 31 Jan 2025 (actual)
- Study completion
- 31 Jan 2025 (actual)
- First posted
- 24 Oct 2022 (actual)
- Results
- Not posted in the source record
Clinical summary
The research question as the sponsor registered it. This describes what the study plans to test, not what it found.
This is a prospective, observational, longitudinal study to assess clinical outcomes in the 12-months following participants' exit from protocol SBM-OWP-03, Delivering Transcutaneous Auricular Neurostimulation to Improve Relapse Prevention in Opioid Use Disorder (RESTORE; ClinicalTrials.gov Identifier: NCT05053503). Clinical outcome scores will be collected at study exit from protocol SBM-OWP-03, 1 month, 3 months, 6 months, 9 months, and 12 months after study exit from protocol SBM-OWP-03.
Study design
- Observational model
- Case only
- Time perspective
- Prospective
- Number of arms
- 2
| Arm | Type | Receives |
|---|---|---|
| Participants randomized to receive tAN therapy in SBM-OWP-03 Phase II | – | Behavioral: Clinical Outcomes and Questionnaires |
| Participants not randomized to receive tAN therapy in SBM-OWP-03 Phase II | – | Behavioral: Clinical Outcomes and Questionnaires |
Who may qualify
- Ages
- 18 to 65 years
- Sex
- All
- Healthy volunteers
- Not accepted
- Age groups
- Adult, Older adult
- Study population
- Participants with a history of dependence on prescription or non-prescription opioids
Key inclusion criteria (3 listed)
- Consented participant for protocol SBM-OWP-03, Delivering Transcutaneous Auricular Neurostimulation to Improve Relapse Prevention in Opioid Use Disorder (RESTORE)
- Participant is English proficient
- Participant is able to provide informed consent and function at an intellectual level sufficient for study requirements
Key exclusion criteria (2 listed)
- Participant is unable to reliably receive and respond to assessments via email or telephone
- Participant has any other significant disease or disorder which, in the opinion of the Investigator, may either put the participants at risk because of participation in the trial, or may influence the result of the trial, or the participant's ability to participate in the trial
Eligibility is decided by the study team after screening; this overview does not establish that a patient qualifies. Full inclusion and exclusion criteria.
Interventions
| Intervention | Type | Arms |
|---|---|---|
| Clinical Outcomes and QuestionnairesClinical patient-reported outcomes will be administered remotely at specified timepoints. No treatment or intervention will be administered in this protocol. | Behavioural | Participants not randomized to receive tAN therapy in SBM-OWP-03 Phase II, Participants randomized to receive tAN therapy in SBM-OWP-03 Phase II |
Primary outcome
Proportion of participants in Phase II with a relapse event
Time frame: 12 months (total duration of trial)
9 secondary outcomes
Proportion of participants in either Phase I or Phase II with a relapse event
Time frame: 12 months (total duration of trial)
Mean change in recovery capital measured by Brief Assessment of Recovery Capital (BARC-10)
Time frame: Baseline to Study Completion (12 months)
Mean change in opioid craving measured by the Opioid Craving Scale (OCS)
Time frame: Baseline to Study Completion (12 months)
Mean change in protracted withdrawal symptoms measured by the Short Opiate Withdrawal Scale-Gossop (SOWS-Gossop)
Time frame: Baseline to Study Completion (12 months)
Mean change in depression symptoms across time measured by Patient Health Questionnaire (PHQ-9)
Time frame: Baseline to Study Completion (12 months)
Mean change in anxiety across time measured by Generalized Anxiety Disorder (GAD-7)
Time frame: Baseline to Study Completion (12 months)
Mean change in PTSD symptoms across time measured by the PTSD Checklist for DSM-5 (PCL-5)
Time frame: Baseline to Study Completion (12 months)
Mean change in Quality of Life across time measured by World Health Organization Quality of Life(WHOQOL-BREF) domain scores
Time frame: Baseline to Study Completion (12 months)
Mean change in Commitment to Sobriety Scale (CSS-5)
Time frame: Baseline to Study Completion (12 months)
Results and safety
The study is completed, but results are not available in the source record. That does not mean the treatment did or did not work.
Research links
- Official record on ClinicalTrials.govLast updated by the sponsor 9 Apr 2025.
- Individual participant dataSharing planned: No
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Referral and contact
AzTrials does not enrol participants or take referrals. Contact the study team or a site listed below; they decide who can take part. This study is not recruiting at the moment.
The record lists no contact. Use the official record to reach the sponsor.
3 sites in 1 country: see every site and its status.
Questions about this trial
What is this clinical trial studying?
An observational study of Opioid Use Disorder and Relapse, run by Spark Biomedical, Inc. at 3 sites 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 3 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 9 Apr 2025. Status can change between updates, so confirm with the study contact before making plans.
Where is the study taking place?
The record lists 3 sites 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?
Proportion of participants in Phase II with a relapse event (time frame: 12 months (total duration of trial)). 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 9 Apr 2025.