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Recruiting NCT05785000

NCT05785000 Rehabilitation in Post Concussion Syndrome

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Clinical Trial Summary
NCT ID NCT05785000
Status Recruiting
Phase
Sponsor Rigshospitalet, Denmark
Condition Post-Concussion Syndrome
Study Type INTERVENTIONAL
Enrollment 70 participants
Start Date 2023-02-01
Primary Completion 2025-08-01

Eligibility & Interventions

Sex All sexes
Min Age 18 Years
Max Age 70 Years
Study Type INTERVENTIONAL
Interventions
Physical exercise programme as an add-onControl patients receiving usual care

Eligibility Fast-Check

Enter your details for a quick preliminary check. This does not replace medical advice.

What to Expect as a Participant

You will actively receive the study intervention — which may be a drug, biologic, device, or procedure.

This trial targets 70 participants in total. It began in 2023-02-01 with a primary completion date of 2025-08-01.

⚠ This information is for research awareness only. Always consult your physician before joining any clinical trial. Participation is voluntary and you may withdraw at any time.

Brief Summary

This project evaluates and quantifies the effects of an individually tailored exercise program applied to patients with long-lasting symptoms after concussion, minor traumatic brain injury, so-called Post-Concussion Syndrome (PCS). The project investigates the phenomenon Post Concussion Syndrome in four dimensions with a focus on both patient perspectives of PCS, an interventional physical program, a neurobiological basis for PCS through Magnetic Resonance Imaging (MRI) and finally through a 360-degree evaluation of the entire project involving patients and scientists in a reflective process.

Eligibility Criteria

Inclusion Criteria: * Post concussion syndrome (PCS) diagnose according to WHO ICD-10 classification and documented by written statement from physician veritying a mild traumatic brain injury * Longer lasting symptoms for at least 4 weeks after initial trauma * If allocated to add-on exercise protocol participant must feel able to prioritize the intervention structure * Communication language must be Danish Exclusion Criteria: * Other diseases blurring the diagnose PCS * Other serious brain diseases * Severe cardiovascular diseases precluding physical activity according to protocol

Contact & Investigator

Central Contact

Henrik BW Larsson, Professor

✉ henrik.bo.wiberg.larsson@regionh.dk

📞 (+45) 24824294

Principal Investigator

Henrik BW Larsson, Professor

PRINCIPAL INVESTIGATOR

Faculty of Health and Medical Science, University of Copenhagen, Denmark

Frequently Asked Questions

Who can join the NCT05785000 clinical trial?

This trial is open to participants of all sexes, aged 18 Years or older, up to 70 Years, studying Post-Concussion Syndrome. Full inclusion and exclusion criteria are listed in the Eligibility Criteria section. Always confirm your eligibility with the research team before applying.

Is NCT05785000 currently recruiting?

Yes, NCT05785000 is actively recruiting participants. Contact the research team at henrik.bo.wiberg.larsson@regionh.dk for enrollment information.

Where is the NCT05785000 trial being conducted?

This trial is being conducted at Copenhagen, Denmark.

Who is sponsoring the NCT05785000 clinical trial?

NCT05785000 is sponsored by Rigshospitalet, Denmark. The principal investigator is Henrik BW Larsson, Professor at Faculty of Health and Medical Science, University of Copenhagen, Denmark. The trial plans to enroll 70 participants.

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