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NCT06901128: Covideo
The Covideo Study - a Trial of Cognitive Therapy for Social Anxiety Disorder in Youth, Comparing Screen to Office Delivery
NA trial testing cognitive therapy in Social Anxiety Disorder (SAD) in 200 participants. Currently enrolling.
31 December 2028
Quick facts
| Lead sponsor | Sykehuset Innlandet HF |
|---|---|
| Phase | NA |
| Status | Recruiting now |
| Study type | INTERVENTIONAL |
| Allocation | randomized |
| Design | parallel |
| Masking | single |
| Primary purpose | treatment |
| Enrollment | 200 |
| Start date | 1 April 2025 |
| Primary completion | 31 December 2028 |
| Estimated completion | 31 December 2035 |
| Sites | 5 locations across Norway |
Drugs / interventions tested
- cognitive therapy
Conditions studied
- Social Anxiety Disorder (SAD) — all drugs for Social Anxiety Disorder (SAD) →
Sponsor
Sykehuset Innlandet HF — full company profile →
Who can join
Adults 14 to 18, any sex, with Social Anxiety Disorder (SAD). Patients with the condition only — healthy volunteers not accepted.
Sponsor's own description
The main goal of this clinical trial is to examine screen delivery as an alternative for offering cognitive therapy to youth with social anxiety. It will examine its effectiveness compared to office delivery, but also its acceptability and sustainability, and identify factors important for the outcome of this approach. The main questions it aims to answer are: Does screen delivery show comparable effectiveness to office delivery? Is screen delivery well accepted by youth and therapists? Does screen delivery show economic and climate sustainability? Do credibility and therapeutic alliance predict therapy outcome? In the study researchers will compare screen delivery to office delivery of cognitive therapy for social anxiety disorders in 200 youth aged 14-18 years. After an initial screening in schools, eligible youth are assessed with a diagnostic interview. Those meeting inclusion criteria will be offered either screen or office therapy. This is decided by random selection (a draw). Participants will: Complete an initial short screening questionnaire. Respond to a diagnostic interview online. Meet their therapist first time in person. Attend 14 weekly 90-minutes therapy session. Complete weekly questionnaires during the therapy. Answer interview and questionnaires after the therapy, and also 6 months, 2 years and 4 years later. Parents are also interviewed and informed of the study.
Publications & conference data
No peer-reviewed publications indexed yet for this trial.
Verify or expand the search:
- PubMed search for NCT06901128
- Europe PMC full search
- ASCO Meeting Library
- ESMO Meeting Library
- bioRxiv preprints
- medRxiv preprints
- Google Scholar
Related trials
Other trials of cognitive therapy
Trials testing the same drug.
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Other recruiting trials for Social Anxiety Disorder (SAD)
Currently open trials in the same condition.
- NCT07228143 — Stepped Care Treatment for Anxiety Resilience · NA · recruiting
- NCT07466277 — Intermittent Theta Burst Stimulation of the Prefrontal Cortex in Social Anxiety Disorder · NA · recruiting
- NCT07533812 — AI-Assisted 4-Week Psychodynamic Therapy and Cognitive Behavioral Therapy Via Smartphone for Social Anxiety: A Randomize · NA · active not recruiting
- NCT06805565 — A Study of ONO-1110 in Patients With Social Anxiety Disorder · Phase 2 · active not recruiting
- NCT07456631 — ACTsocially: The (Dis)Similarities of ACT for Changing Internalizing and Externalizing Symptomatology in Adolescence · NA · recruiting
Other Sykehuset Innlandet HF trials
Trials by the same sponsor.
- NCT06790186 — Improving Real-world Function for Persons with Schizophrenia: a Single-case Experimental Design · NA · not yet recruiting
- NCT06403423 — Screening for Aortic Aneurysms in Inland Norway · enrolling by invitation
- NCT05874791 — Executive Control Training for Adolescents With ADHD: A Randomized Controlled Effectiveness Trial · NA · active not recruiting
- NCT07375615 — Continous Glucose Monitoring in Neonates at Risk of Hypoglycaemia- a Feasibility Study · completed
- NCT05651659 — Preventing and Approaching Crises for Frail Community-dwelling Patients Through Through Innovative Care (PRACTIC) · NA · active not recruiting
Verify against primary sources
- ClinicalTrials.gov — authoritative US registry record
- WHO ICTRP — international registry index
- EU Clinical Trials Register
- Sponsor press releases (Google)
- Trial protocol + status: ClinicalTrials.gov NCT06901128 (US National Library of Medicine, public domain)
- Drug + disease cross-links: matched in real time against Drug Landscape's normalised drug + company + condition tables
- Sponsor: as reported to ClinicalTrials.gov by Sykehuset Innlandet HF
- Last refreshed: 28 March 2025
Drug Landscape aggregates and links these public records for informational use only. Always verify against the primary source before clinical or regulatory decisions. Canonical URL: https://druglandscape.com/trial/NCT06901128.
Primary sources · FDA · ClinicalTrials.gov · EMA · SEC EDGAR · ChEMBL · Wikidata · full sourcing