Tobias Jung

Dr. Tobias Jung


Research Focus & Metrics

Academic Career Length

19Years (2008-Present)

(Calculated once Scilit publication data is synced: current year − year of first publication + 1)

Representative Publications

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CGClemens Gwinner
Clemens Gwinner
Sven MaerdianSven Maerdian
Sven Maerdian
PSPhilipp Schwabe
Philipp Schwabe
KSKlaus-D. Schaser
Klaus-D. Schaser
BKBjörn Dirk Krapohl
Björn Dirk Krapohl
TJTobias Jung
Tobias Jung

Verified
Journal Article
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SFStephen Fahy
Stephen Fahy
SOStephan Oehme
Stephan Oehme
DMDanko Dan Milinkovic
Danko Dan Milinkovic
TJTobias Jung
Tobias Jung
BBBenjamin Bartek
Benjamin Bartek
The aim of our study was to evaluate the potential role of Artificial Intelligence tools like ChatGPT in patient education. To do this, we assessed both the quality and readability of information provided by ChatGPT 3.5 and 4 in relation to Anterior Cruciate Ligament (ACL) injury and treatment. ChatGPT 3.5 and 4 were used to answer common patient queries relating to ACL injuries and treatment. The quality of the information was assessed using the DISCERN criteria. Readability was assessed with the use of seven readability formulae: the Flesch–Kincaid Reading Grade Level, the Flesch Reading Ease Score, the Raygor Estimate, the SMOG, the Fry, the FORCAST, and the Gunning Fog. The mean reading grade level (RGL) was compared with the recommended 8th-grade reading level, the mean RGL among adults in America. The perceived quality and mean RGL of answers given by both ChatGPT 3.5 and 4 was also compared. Both ChatGPT 3.5 and 4 yielded DISCERN scores suggesting “good” quality of information, with ChatGPT 4 slightly outperforming 3.5. However, readability levels for both versions significantly exceeded the average 8th-grade reading level for American patients. ChatGPT 3.5 had a mean RGL of 18.08, while the mean RGL of ChatGPT 4 was 17.9, exceeding the average American reading grade level by 10.08 grade levels and 9.09 grade levels, respectively. While ChatGPT can provide both reliable and good quality information on ACL injuries and treatment options, the readability of the content may limit its utility. Additionally, the consistent lack of source citation represents a significant area of concern for patients and clinicians alike. If AI is to play a role in patient education, it must reliably produce information which is accurate, easily comprehensible, and clearly sourced.

9 June 2014 in Arthroscopy Techniques
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Journal Article
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CGClemens Gwinner
Clemens Gwinner
SKSebastian Kopf
Sebastian Kopf
AHArnd Hoburg
Arnd Hoburg
NHNorbert P. Haas
Norbert P. Haas
TJTobias Jung
Tobias Jung
Avulsion fracture of the posterior cruciate ligament from its tibial insertion is a rare condition. Early surgical treatment has been regarded as necessary, but the optimal surgical technique remains unclear. The purpose of this technical note is to present a novel all‐inside arthroscopic reconstruction technique for bony tibial avulsion fractures of the posterior cruciate ligament using the TightRope device (Arthrex, Naples, FL). Technique Video: video See video under supplementary data.

20 December 2010 in Arthroscopy
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TJTobias Jung
Tobias Jung
ALAnne Lubowicki
Anne Lubowicki
AWAnna Wienand
Anna Wienand
MWMichael Wagner
Michael Wagner
AWAndreas Weiler
Andreas Weiler

13 August 2019 in Trials
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DNDaniel Niederer
Daniel Niederer
MKMatthias Keller
Matthias Keller
AAAndrea Achtnich
Andrea Achtnich
RARalph Akoto
Ralph Akoto
AAAtesch Ateschrang
Atesch Ateschrang
TSThomas Stein
Thomas Stein
Although anterior cruciate ligament (ACL) tear-prevention programs may be effective in the (secondary) prevention of a subsequent ACL injury, little is known, yet, on their effectiveness and feasibility. This study assesses the effects and implementation capacity of a secondary preventive motor-control training (the Stop-X program) after ACL reconstruction. A multicenter, single-blind, randomized controlled, prospective, superiority, two-arm design is adopted. Subsequent patients (18–35 years) with primary arthroscopic unilateral ACL reconstruction with autologous hamstring graft are enrolled. Postoperative guideline rehabilitation plus Classic follow-up treatment and guideline rehabilitation plus the Stop-X intervention will be compared. The onset of the Stop-X program as part of the postoperative follow-up treatment is individualized and function based. The participants must be released for the training components. The endpoint is the unrestricted return to sport (RTS) decision. Before (where applicable) reconstruction and after the clearance for the intervention (aimed at 4–8 months post surgery) until the unrestricted RTS decision (but at least until 12 months post surgery), all outcomes will be assessed once a month. Each participant is consequently measured at least five times to a maximum of 12 times. Twelve, 18 and 24 months after the surgery, follow-up-measurements and recurrence monitoring will follow. The primary outcome assessement (normalized knee-separation distance at the Drop Jump Screening Test (DJST)) is followed by the functional secondary outcomes assessements. The latter consist of quality assessments during simple (combined) balance side, balance front and single-leg hops for distance. All hop/jump tests are self-administered and filmed from the frontal view (3-m distance). All videos are transferred using safe big content transfer and subsequently (and blinded) expertly video-rated. Secondary outcomes are questionnaires on patient-reported knee function, kinesiophobia, RTS after ACL injury and training/therapy volume (frequency – intensity – type and time). All questionnaires are completed online using the participants’ pseudonym only. Group allocation is executed randomly. The training intervention (Stop-X arm) consists of self-administered home-based exercises. The exercises are step-wise graduated and follow wound healing and functional restoration criteria. The training frequency for both arms is scheduled to be three times per week, each time for a 30 min duration. The program follows current (secondary) prevention guidelines. Repeated measurements gain-score analyses using analyses of (co-)variance are performed for all outcomes. German Clinical Trials Register, identification number DRKS00015313 . Registered on 1 October 2018.

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CGClemens Gwinner
Clemens Gwinner
AHArnd Hoburg
Arnd Hoburg
SWSophie Wilde
Sophie Wilde
ISImke Schatka
Imke Schatka
BKBjörn Dirk Krapohl
Björn Dirk Krapohl
TJTobias Jung
Tobias Jung