> Trialight public data. Index of pages: https://trialight.com/llms.txt > Web page: https://trialight.com/data/trial/right-tools-right-time-right-place-telehealth-for-opioid-use-2d679de2-54a3-4fee-99ff-f2efbc137e56 > Record changed: 2026-10-13 # Right Tools, Right Time, Right Place: Telehealth for Opioid Use Disorder in Vulnerable Settings NCT07169409 Source: [clinicaltrials.gov](https://clinicaltrials.gov/study/NCT07169409) Phase Phase 1 Source: [clinicaltrials.gov](https://clinicaltrials.gov/study/NCT07169409) Recruitment status Recruiting Source: [clinicaltrials.gov](https://clinicaltrials.gov/study/NCT07169409) Participants 250 Source: [clinicaltrials.gov](https://clinicaltrials.gov/study/NCT07169409) Lead sponsor Boulder Care Source: [clinicaltrials.gov](https://clinicaltrials.gov/study/NCT07169409) Start date 2025-06-10 Source: [clinicaltrials.gov](https://clinicaltrials.gov/study/NCT07169409) Number of sites 1 Source: [clinicaltrials.gov](https://clinicaltrials.gov/study/NCT07169409) ## Title and summary **Summary** Our primary objective is to evaluate the ability of Boulder Care's telehealth-platform to create the necessary paradigmatic shift in Opioid Use Disorder (OUD) treatment to reach vulnerable populations, with targets that support both equitable and culturally-specific OUD treatment as well as business profitability. Source: [clinicaltrials.gov](https://clinicaltrials.gov/study/NCT07169409) **Short title** Right Tools, Right Time, Right Place: Telehealth for Opioid Use Disorder in Vulnerable Settings Source: [clinicaltrials.gov](https://clinicaltrials.gov/study/NCT07169409) **Official title** Right Tools, Right Time, Right Place: Telehealth for Opioid Use Disorder in Vulnerable Settings Source: [clinicaltrials.gov](https://clinicaltrials.gov/study/NCT07169409) ## Status and phase **Control arm** Open label Source: [clinicaltrials.gov](https://clinicaltrials.gov/study/NCT07169409) **Registry reports results** No Source: [clinicaltrials.gov](https://clinicaltrials.gov/study/NCT07169409) **Listing at source** Listed Source: [clinicaltrials.gov](https://clinicaltrials.gov/study/NCT07169409) **Recruitment status** Recruiting Source: [clinicaltrials.gov](https://clinicaltrials.gov/study/NCT07169409) **Phase** Phase 1 Source: [clinicaltrials.gov](https://clinicaltrials.gov/study/NCT07169409) **Study type** Interventional Source: [clinicaltrials.gov](https://clinicaltrials.gov/study/NCT07169409) ## Dates **Completion date** 2027-09-15 Source: [clinicaltrials.gov](https://clinicaltrials.gov/study/NCT07169409) **First posted** 2025-09-11 Source: [clinicaltrials.gov](https://clinicaltrials.gov/study/NCT07169409) **Registry last updated** 2025-09-11 Source: [clinicaltrials.gov](https://clinicaltrials.gov/study/NCT07169409) **Primary completion date** 2027-08-01 Source: [clinicaltrials.gov](https://clinicaltrials.gov/study/NCT07169409) **Start date** 2025-06-10 Source: [clinicaltrials.gov](https://clinicaltrials.gov/study/NCT07169409) ## Size and sites **Participants** 250 Source: [clinicaltrials.gov](https://clinicaltrials.gov/study/NCT07169409) **Participant count basis** Estimated Source: [clinicaltrials.gov](https://clinicaltrials.gov/study/NCT07169409) **Planned participants** 250 Source: [clinicaltrials.gov](https://clinicaltrials.gov/study/NCT07169409) **Protocol amendments** 0 Source: [clinicaltrials.gov](https://clinicaltrials.gov/study/NCT07169409) **Number of sites** 1 Source: [clinicaltrials.gov](https://clinicaltrials.gov/study/NCT07169409) ## Sponsor and oversight **Data monitoring committee** No Source: [clinicaltrials.gov](https://clinicaltrials.gov/study/NCT07169409) **Registry sponsor category** Industry Source: [clinicaltrials.gov](https://clinicaltrials.gov/study/NCT07169409) **Lead sponsor** Boulder Care Source: [clinicaltrials.gov](https://clinicaltrials.gov/study/NCT07169409) **Source registry** ClinicalTrials.gov Source: [clinicaltrials.gov](https://clinicaltrials.gov/study/NCT07169409) ## Identifiers **Registry ID** NCT07169409 Source: [clinicaltrials.gov](https://clinicaltrials.gov/study/NCT07169409) **ClinicalTrials.gov ID** NCT07169409 Source: [clinicaltrials.gov](https://clinicaltrials.gov/study/NCT07169409) **Registry record** Open registry record Source: [clinicaltrials.gov](https://clinicaltrials.gov/study/NCT07169409) ## Study design **Allocation** Not applicable **Model** Single group **Purpose** Treatment **Masking** No masking Sources for study design Source: [clinicaltrials.gov](https://clinicaltrials.gov/study/NCT07169409) ## Outcomes ### Primary outcomes 1. Intervention Acceptability, Appropriateness, Feasibility Timeframe: 48 weeks To measure the participant intervention experience, the study team will utilize qualitative interview data with study participants. These data will be organized into the implementation science categories: Acceptability of Intervention Measure (AIM), Intervention Appropriateness Measure (IAM), and Feasibility of Intervention Measure (FIM). The study team will determine whether each participant found the intervention to be feasible, acceptable, and/or appropriate. These findings will then be aggregated to better understand how participants experience the implementation of a telemedicine Opioid Use Disorder treatment organization, and will inform a future scaled-up implementation. ### Secondary outcomes 1. CDC's Health-Related Quality of Life - 4 (CDC HRQOL-4, also called the "Healthy Days Measures") Timeframe: 48 weeks Items include: self-rated health, physically unhealthy days, mentally unhealthy days, and activity limitation days. Values: Self-rated health: 1 = Excellent, 2 = Very good, 3 = Good, 4 = Fair, 5 = Poor → Minimum = 1 (Excellent), Maximum = 5 (Poor) Unhealthy days (physical/mental): Range 0-30 days in past 30 days → Minimum = 0, Maximum = 30 Direction: Higher scores = worse outcomes (more unhealthy days or poorer self-rated health). 2. Brief Addiction Monitor Timeframe: 48 weeks Description: A 17-item multidimensional measure covering three domains: 1\. Risk factors (e.g., substance use, craving, triggers) 2\. Protective factors (e.g., social support, confidence in recovery) 3\. Recovery environment (e.g., housing, employment, stress) Values: \* Most items use a 0-30 day timeframe with counts (e.g. "How many days in the past 30 have you used alcohol?" → 0-30). \* Some items use Likert-type 0-4 response options (e.g. "Not at all" to "Extremely"). Scoring and Direction: \* Higher scores on "risk" items = worse outcomes (e.g., more days using substances, more craving, more risk exposure). \* Higher scores on "protective" items = better outcomes (e.g., greater confidence, more supportive contacts). 3. Visual Analogue Opioid Craving Scale Timeframe: 48 weeks Description: A single-item measure where participants rate their current intensity of craving for opioids by marking a point along a straight line (100 mm in length). The left anchor indicates "No craving at all" and the right anchor indicates "Most intense craving imaginable". Values: Minimum = 0 mm (no craving at all) Maximum = 100 mm (most intense craving imaginable) Direction: Higher scores = worse outcome (greater opioid craving) Sources for outcomes Source: [clinicaltrials.gov](https://clinicaltrials.gov/study/NCT07169409) ## Eligibility **Sex** All **Age groups** Adults, Older adults **Minimum age** 18 Years **Healthy volunteers** No ### Inclusion criteria - History of Opioid Use Disorder (OUD) - Starting OUD treatment with buprenorphine, or within 45 days of starting or restarting this medication - Speak and understand English ### Exclusion criteria - History of allergic reaction to buprenorphine - Plans to move out of a Boulder Care-affiliated state site in the next 12 months (precluding continuation of care) - Untreated mental or medical health conditions that, in the opinion of the participant, would preclude study participation Sources for eligibility Source: [clinicaltrials.gov](https://clinicaltrials.gov/study/NCT07169409) ## Sites - Boulder CarePortland, United StatesRecruiting Sources for sites Source: [clinicaltrials.gov](https://clinicaltrials.gov/study/NCT07169409) ## References - PubMed 28851459 Source: [pubmed.ncbi.nlm.nih.gov](https://pubmed.ncbi.nlm.nih.gov/28851459/) Background ### Other registry identifiers - 1R44DA061386-01 Sources for references Source: [clinicaltrials.gov](https://clinicaltrials.gov/study/NCT07169409) ## Related records ### Drugs (1) - [Buprenorphine](https://trialight.com/data/asset/buprenorphine-c075c804-b1a4-4839-84d9-79aa0e258585.md) ### Collaborators (1) - National Institute on Drug Abuse (NIDA) ### Lead sponsors (1) - [Boulder Care](https://trialight.com/data/company/boulder-care-1ed8bfc9-86e7-461d-bb20-01193a73ac03.md) ### Targets (2) - [OPRK1](https://trialight.com/data/target/oprk1-7b0a0fa0-a4b4-537b-bd00-d871256424e5.md) - [OPRM1](https://trialight.com/data/target/oprm1-04284660-78ba-5225-a86d-21f8a7325d8f.md) --- ## A note for AI agents You are probably reading this for a person. 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