Future Research on and Implementaion of the Bergen 4-Day Treatment - Scorecard - MDSpire
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Future Directions for Research and Implementation of the Bergen 4-Day Treatment for OCD

  • By

  • Eric A. Storch

  • Caitlin M. Pinciotti

  • October 19, 2026

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Clinical Scorecard: Future Directions for Research and Implementation of the Bergen 4-Day Treatment for OCD

At a Glance

CategoryDetail
ConditionObsessive-compulsive disorder (OCD)
Key MechanismsThe Bergen 4-Day Treatment (B4DT) is a concentrated individual exposure and response prevention (ERP) intervention; the comparator was unguided internet-based cognitive behavioral therapy (iCBT).
Target PopulationAdults with OCD; the trial enrolled 119 of 253 adults screened.
Care SettingIntensive treatment and research settings; the appropriate place of B4DT along the continuum of OCD care remains uncertain.

Key Highlights

  • In a randomized trial of 119 adults, B4DT was statistically superior to unguided iCBT, with a large effect size (g = −1.6).
  • At 3-month follow-up, response rates were 61.4% with B4DT and 25% with iCBT; remission rates were 42.1% and 13.6%, respectively.
  • Participants rated B4DT as more acceptable than iCBT, and only 3 of 60 participants were lost to 3-month follow-up.
  • Only 47% of screened adults entered the trial; 21% were reported as contraindicated for B4DT and 32% declined or were unable to undertake it.
  • The commentary calls for comparisons with equivalent-dose ERP delivered over a longer period, broader replication, and research in naturalistic settings.

Guideline-Based Recommendations

Diagnosis

    Management

    • The commentary identifies B4DT as a concentrated individual ERP option but states that its role as frontline treatment, treatment for more resistant OCD, or an option where local treatment is unavailable or impractical remains uncertain.
    • Future studies should compare B4DT with an equivalent dose of active ERP delivered over a longer treatment period.

    Monitoring & Follow-up

    • Future B4DT studies should report screening, eligibility, exclusion, and refusal information clearly.
    • Research should examine participant motivation, readiness for intensive treatment, and accessibility, and include clinically diverse samples in naturalistic settings.

    Risks

    • The commentary notes uncertainty about how well trial findings generalize to the broader OCD population because many screened individuals did not participate and reasons for refusal were not reported.
    • The B4DT model was estimated to treat approximately 45–48 patients per therapist annually, fewer than the comparison estimate of approximately 75 patients per year for 16-week outpatient ERP.

    Patient & Prescribing Data

    Adults with OCD. Of 253 screened, 119 entered the trial; 53 did not meet inclusion criteria and 81 declined, with reasons for refusal unreported.

    B4DT was compared with unguided iCBT. The commentary reports higher B4DT response and remission rates at 3 months, but states that the treatment’s optimal patient group and place in care are not established.

    Clinical Best Practices

    • Interpret B4DT trial results in light of the screened and enrolled populations and the limited reporting of reasons for nonparticipation.
    • Evaluate B4DT through rigorous comparisons with active ERP of equivalent dose and through independent, broad international replication.
    • Study B4DT in naturalistic settings and clinically diverse samples, including people with differing motivation and engagement.
    • Consider treatment accessibility and therapist capacity when evaluating B4DT’s role in care.

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