Last reviewed · How we verify
NCT04371211: BICS-T I
Telemedicine Brain Injury Coping Skills (BICS-T) Support Group for Brain Injury Survivors and Their Caregivers
NA trial testing Telemedicine Brain Injury Coping Skills in Traumatic Brain Injury in 13 participants. Completed in 1 January 2020.
1 December 2019
Quick facts
| Lead sponsor | Rehabilitation Hospital of Indiana |
|---|---|
| Phase | NA |
| Status | Completed |
| Study type | INTERVENTIONAL |
| Allocation | na |
| Design | single group |
| Masking | none |
| Primary purpose | treatment |
| Enrollment | 13 |
| Start date | 20 September 2018 |
| Primary completion | 1 December 2019 |
| Estimated completion | 1 January 2020 |
| Sites | 1 location across United States |
Drugs / interventions tested
- Telemedicine Brain Injury Coping Skills
Conditions studied
- Traumatic Brain Injury — all drugs for Traumatic Brain Injury →
- Coping Skills — all drugs for Coping Skills →
Sponsor
Rehabilitation Hospital of Indiana
Who can join
18 and older, any sex, with Traumatic Brain Injury or Coping Skills. Patients with the condition only — healthy volunteers not accepted.
Sponsor's own description
Brain Injury can be devastating for both patients and family members and can result in chronic difficulties in vocational, social, financial, as well as physical functioning. The occurrence of emotional and neurobehavioral challenges in individuals with brain injury is also common with research consistently showing links between these challenges and a person's overall rehabilitation outcome. In order to provide patients and caregivers greater support and teach adaptive coping strategies, the authors of this grant designed and studied a coping skills group specifically for brain injury survivors and their caregivers at the Rehabilitation Hospital of Indiana (RHI) called the Brain Injury Coping Skills group (BICS). BICS is a 12 session (one session per week), manualized, cognitive-behavioral treatment group designed to provide support, coping skills, and psychoeducation aimed to improve perceived self-efficacy (PSE) and emotional functioning.
Publications & conference data
No peer-reviewed publications indexed yet for this trial. Completed trials usually publish results within 12-18 months.
Verify or expand the search:
- PubMed search for NCT04371211
- Europe PMC full search
- ASCO Meeting Library
- ESMO Meeting Library
- bioRxiv preprints
- medRxiv preprints
- Google Scholar
Related trials
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Other Rehabilitation Hospital of Indiana trials
Trials by the same sponsor.
- NCT05185635 — Validating Neuropsych Tests in Spanish-speakers · NA · unknown
- NCT04386681 — Re-entry Continuum for Brain Injury · NA · active not recruiting
- NCT04371120 — Brain Injury Self-Efficacy Scale Validation · terminated
- NCT04462549 — Improving Health Outcomes With Resource Facilitation · NA · completed
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 NCT04371211 (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 Rehabilitation Hospital of Indiana
- Last refreshed: 25 November 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/NCT04371211.
Primary sources · FDA · ClinicalTrials.gov · EMA · SEC EDGAR · ChEMBL · Wikidata · full sourcing