Submitted:
16 October 2025
Posted:
22 October 2025
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Abstract
Background: The opioid epidemic remains a prominent public health issue across the United States, with growing incidence rates of Opioid Use Disorder (OUD) and overdose fatalities. Medication-Assisted Treatment (MAT), which involves FDA-authorized medications, along with counseling and behavioral therapies, is a high standard for OUD treatment. Stigma, shortage of available providers, and regulatory complications, however, hold back its availability. Telehealth, which enables remote treatment delivery, offers a scalable solution to address these limitations, particularly in underserved rural areas. Objective: This systematic review and meta-analysis analyzed the effectiveness, practice, and patient outcomes of telehealth-delivered MAT for OUD compared with traditional in-person treatment modes. Methods: Following the PRISMA guidance and Cochrane Handbook recommendations, electronic literature searches were conducted in PubMed, Scopus, Web of Science, and Cochrane Library for publications up to April 2024. Qualified studies assessed telehealth-delivered MAT and provided data on patient retention, overdose, or other relevant endpoints. Design-specific risk of bias tools were used for the risk of bias assessment, while a random-effects DerSimonian–Laird model was used to pool the data. Results: Thirty-three studies were included. Telehealth MAT improved patient retention compared with in-person MAT (log OR=0.32, 95% CI: [-1.09, 1.73]), was associated with a moderate reduction in overdose risk (pooled effect size 0.66, 95% CI: [0.19, 1.13]), and showed beneficial effects for co-occurring substance use disorders (log OR=0.28, 95% CI: [0.04, 0.52]) and mental health conditions such as major Depression (log OR=0.44, 95% CI: [0.03, 0.84]) and bipolar disorder (log OR=0.44, 95% CI: [0.05, 0.84]). Conclusion: Telehealth-enabled MAT is more effective for treatment retention, less likely to lead to overdose, and combines mental health care with OUD management. These results justify the perseverance in policy efforts to maintain telehealth prescription flexibility and enhance broadband infrastructure, both of which serve to reduce treatment disparities. Research needs assessments alone are insufficient to evaluate long-term effectiveness, cost-effectiveness, and patient experience.
Keywords:
Plain Language Summary
Introduction
Rationale
Objectives
- Assess treatment retention rates among patients receiving telehealth MAT compared with in-person MAT.
- Evaluate overdose outcomes associated with telehealth-delivered MAT.
- Examine additional clinical and behavioral outcomes, including comorbid substance use disorders, major Depression, and bipolar disorder.
- Characterize the implementation modalities of telehealth MAT (e.g., video, phone, and mobile platforms) and associated barriers or facilitators.
- Synthesizing evidence on equity and access emphasizes the role of broadband connectivity, digital literacy, and regulatory frameworks.
- Inform policy and practice by identifying evidence-based recommendations for sustaining telehealth by prescribing flexibilities and promoting equitable access to OUD treatment.
Methods
Eligibility Criteria
- Population (P): Individuals diagnosed with Opioid Use Disorder (OUD), including adults and adolescents, receiving clinical Treatment for opioid dependence or misuse.
- Intervention (I): Telehealth-delivered Medication-Assisted Treatment (MAT), including remote initiation, monitoring, and maintenance using audio, video, or digital communication platforms (e.g., telemedicine, telepsychiatry, mobile health applications).
- Comparison (C): Conventional in-person MAT delivery or pre-intervention baseline (for single-arm or before–and–after designs).
- Outcomes (O): The primary outcomes included treatment retention and overdose. The secondary outcomes included other substance use disorders, major Depression, and bipolar disorder. Studies that reported patient satisfaction, program engagement, and access disparities were also considered in the qualitative synthesis.
- Study designs: Randomized controlled trials, quasi-experimental studies, cohort, cross-sectional, qualitative, mixed-methods, and implementation research designs.
- Setting: Outpatient, community, correctional, or primary care settings where MAT was provided.
- Language: English only.
- Timeframe: All studies published up to April 2024.
- A rapid search update was conducted on September 30, 2025, using PubMed
Exclusion Criteria
- Studies did not focus on OUD or MAT (e.g., alcohol and tobacco-only studies).
- Interventions without a telehealth component (e.g., mobile app without provider contact).
- Conference abstracts, commentaries, and non-peer-reviewed reports.
- Non-English publications.
Information Sources
- PubMed (MEDLINE)
- Scopus
- Web of Science (WOS)
- Cochrane Library
- Opioid Use Disorder (e.g., “opioid crisis,” “OUD,” “narcotic addiction”)
- Medication-Assisted Treatment (e.g., “buprenorphine,methadone,naltrexone”) and
- Telehealth modalities (e.g., “telemedicine,digital health,virtual care,” and e-health”).
Search Strategy
Study Selection
Data Extraction Process
Effect Measures
Synthesis Methods
Statistical Analysis
- Primary outcome: Treatment retention was analyzed using both double-arm comparisons (telehealth vs. in-person; log odds ratio as an effect measure) and single-arm retention rates summarized as weighted proportions.
- Secondary outcomes: Drug overdose, other substance use disorders, major Depression, and bipolar disorder were analyzed using relative risks (RR) or log odds ratios (log OR), depending on data availability.
Risk of Bias Assessment
Reporting Bias Assessment
Certainty Assessment
- Risk of bias,
- Inconsistency,
- Indirectness,
- Imprecision, and
- Publication bias,
| Outcome | No. of Studies (n) | Study Design | Risk of Bias | Inconsistency | Indirectness | Imprecision | Publication Bias | Overall Certainty (GRADE) | Summary of Findings |
|---|---|---|---|---|---|---|---|---|---|
| Treatment Retention | 20 | RCTs, Cohort, Cross-sectional | Not serious | Moderate (I² = 71%) | Not serious | Moderate (wide CI) | None detected | Moderate | Telehealth MAT showed similar or higher retention than in-person MAT (log OR = 0.32, 95% CI [–1.09, 1.73]); consistent direction of effect across study types. |
| Overdose Risk | 14 | Cohort, Cross-sectional | Some concerns | High (I² = 87.8%) | Not serious | Serious (wide CI, few events) | None detected | Low–Moderate | Telehealth MAT associated with moderate reduction in overdose (ES = 0.66, 95% CI [0.19, 1.13]); heterogeneity likely due to population and contextual variability. |
| Other Substance Use Disorders (SUDs) | 6 | Observational | Serious | High (I² = 99.6%) | Not serious | Serious | Possible | Low | Telehealth MAT associated with improved management of other SUDs (log OR = 0.28, 95% CI [0.04, 0.52]); evidence limited by extreme heterogeneity and few studies. |
| Major Depression | 5 | Observational | Some concerns | High (I² = 99.9%) | Not serious | Serious | Possible | Low | Telehealth MAT associated with reduction in depressive symptoms (log OR = 0.44, 95% CI [0.03, 0.84]); findings influenced by one large study (Frost 2022). |
| Bipolar Disorder | 4 | Observational | Serious | High (I² = 99.7%) | Not serious | Serious | Possible | Low | Telehealth MAT may improve bipolar symptoms (log OR = 0.44, 95% CI [0.05, 0.84]); effect consistent in direction but based on few studies. |
- Certainty ratings followed the GRADE approach (High, Moderate, Low, Very Low).
- Evidence for retention and overdose outcomes is more robust because of higher study counts and mixed RCT inclusion.
- Downgrades were applied for inconsistency (high heterogeneity) and imprecision (wide confidence intervals).
- Publication bias appears to be minimal, based on visual inspection of funnel plots and Egger’s regression.
- Further RCTs with standardized telehealth models and longer follow-up periods are needed to strengthen the certainty, particularly for psychiatric comorbidities.
Results
- Study Selection
| Outcome Domain | Studies Reporting Effect (n/33) | Direction of Effect | Pooled Effect (95% CI) | Interpretation |
| Retention rate | 20 / 33 (61%) | ↑ Improved | log OR = 0.32 [–1.09, 1.73] | Comparable or superior to in-person MAT |
| Overdose risk | 14 / 33 (42%) | ↓ Reduced | ES = 0.66 [0.19, 1.13] | Moderate risk reduction |
| Other substance use disorders | 6 / 33 (18%) | ↓ Reduced | log OR = 0.28 [0.04, 0.52] | Additional benefit beyond OUD |
| Major Depression | 5 / 33 (15%) | ↓ Reduced | log OR = 0.44 [0.03, 0.84] | Improved depressive symptoms |
| Bipolar disorder | 4 / 33 (12%) | ↓ Reduced | log OR = 0.44 [0.05, 0.84] | Potential benefit, high heterogeneity |
Study Characteristics
Risk of Bias in Included Studies
Types of Telehealth and MAT
Geographic and Demographic Scope
Population Characteristics
Outcomes Assessed
- Primary Outcome
- Retention Rate
- Cohort Subgroup: This subgroup was moderately heterogeneous (I² = 20.54%), with a non-significant test for heterogeneity (p = 0.24). The effect sizes were homogeneous across studies, reflecting the steady retention rates for this subgroup.
- Cross-sectional Subgroup: This subgroup showed no heterogeneity (I² = 0.00%) and a non-significant test for heterogeneity (p = 0.54). The effect sizes were highly homogeneous, indicating similar retention rates between the studies included in this subgroup.
- Overall, the analysis revealed moderate heterogeneity (I² = 53.86%), which was not statistically significant (P = 0.07). The considerable test of group differences (p = 0.02) indicates that the effect sizes differ between the subgroups "Cohort" and "Cross-sectional.”
Secondary Outcomes
Effectiveness of Telehealth MAT
Adoption of Telehealth for MAT
Comparative Analysis
Quality Assessment
Certainty of the Evidence (GRADE)
Discussions
Principal Findings
Synthesis with Previous Research
Drivers and Barriers to Adoption
Policy and Practice Implications
Digital Equity Considerations
Strengths and Limitations
Future Research Directions
Conclusions
Supplementary Materials
Author Contributions
Funding
Data Availability, Protocol and Supplementary Materials
Ethics and Transparency Statement
Conflicts of Interest
Abbreviations
- A.A. – Akorede Adekoya
- K.A. – Kola Adegoke
- N.D. – Nneka Duru
- Ag. – Abimbola Adegoke
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