Effects of Transcranial Direct Current Stimulation on Cognitive Rehabilitation in Schizophrenia
A legfontosabb adatok
- Ki végzi
- Medical University of Lodz
- Hol
- Lodz (Lengyelország)A helyszín megnézése
- Azonosító
- Állapot
- Csak meghívásos
- Résztvevők
- 120 fő, tervezett
- Kezdés
- 2023. okt. 1.
- Várható befejezés
- 2027. dec. 3.
- A vizsgálat típusa
- Beavatkozással járó, 2 csoportAz egyik csoport egy már használt kezelést kap, összehasonlításként.
- A vizsgált kezelések
- active tDCS
- sham tDCS
- A regiszteradat frissítve
- 2026. január 13.
Ki vehet részt
MI-összefoglaló
A vizsgálat saját részvételi feltételeiből. Gép olvasta ki az oldalon álló regiszterszövegből, ezért tévedhet. Hogy ki vehet részt, azt a lenti regiszterszöveg és a vizsgálat csapata dönti el.
A vizsgálat stabil mentális állapotú, skizofréniával élő felnőtteket keres. Azt vizsgálja, hogy a számítógépes memória- és figyelemtréning előtti enyhe agyi stimuláció javítja-e a gondolkodási képességeket.
- Életkor
- 18-65 év
- Nem
- Minden nem
- A betegség stádiuma
- DSM-5 szerint diagnosztizált skizofrénia; mentálisan stabil állapot. A gyógyszeres kezelés megengedett.
- Korábbi kezelés
- Jelenleg nem kap elektrokonvulzív kezelést (ECT). A skizofrénia elleni gyógyszer szedése folytatható.
A részvétel fő kizáró okai
- Beültetett elektronikus eszköz vagy fém implantátum a fejben
- Korábbi rohamok
- Terhesség
- Eszméletvesztéssel járó fejsérülés vagy agyműtét az elmúlt hat hónapban
- Korábbi szélütés, értágulat, agydaganat, migrén vagy szerhasználat
A regiszter feltételei, szó szerint
Mind a 10 feltétel megnézéseKevesebb
Ki vehet részt
- Adults aged 18-65 years with schizophrenia diagnosed according to DSM-5 criteria (Diagnostic and Statistical Manual of Mental Disorders, Fifth Edition)
- Ability to provide informed consent for tDCS treatment and use of collected data for research purposes
- Mentally stable, may receive pharmacological treatment
Ki nem vehet részt
- Head injury with loss of consciousness or neurosurgery performed within the previous six months
- Currently receiving electroconvulsive therapy (ECT); Withdrawal criteria: participation will be discontinued if any of the following occur:; Urgent medical issues Serious adverse events or side effects Participant unwillingness to continue in the trial
- Contraindications to tDCS, including:; Implanted electronic devices Metal implants in the head History of seizures Contact allergy to materials used for tDCS stimulation (electrodes)
- History of stroke, aneurysm, brain tumor, or other conditions causing increased intracranial pressure
- Pregnancy
- Migraines
- Substance abuse
Nézd meg, megfelelhetsz-e
Magadról válaszolj. Ez nem döntés: hogy részt vehetsz-e, azt csak a vizsgálat csapata mondhatja meg.
- 18 és 65 év között vagy?
Helyszínek itt: Lengyelország
- Department of Old Age Psychiatry and Psychotic DisordersLodz, LengyelországNo longer taking part
A vizsgálatról
Mit akar kideríteni a vizsgálat
The aim of this prospective, randomized, double-blind, placebo-controlled study is to assess whether transcranial direct current stimulation (tDCS) applied prior to RehaCom cognitive training can improve cognitive functioning in individuals diagnosed with schizophrenia.
A teljes eredeti leírásKevesebb
The study is designed to answer the following main questions:
* Does the combination of active tDCS and RehaCom cognitive training lead to better performance on CANTAB tests compared to training preceded by sham stimulation? * Does tDCS enhance the effectiveness of cognitive rehabilitation by strengthening neuroplasticity mechanisms? Researchers will compare the group receiving active tDCS + RehaCom with the group undergoing sham stimulation + RehaCom to determine whether active stimulation produces greater improvements in cognitive functioning.
Participants will receive tDCS targeting the DLPFC, which was selected due to its key involvement in executive cognitive functions. These include working memory, planning, decision-making, inhibitory control, and the regulation of attention, all of which are relevant for modulating cognitive dysfunction in schizophrenia.
The tDCS will be administered using a battery-powered direct current stimulator (DC-Stimulator PLUS, neuroCare, Germany) through two saline-soaked sponge electrodes (5 cm × 7 cm). According to the International 10-20 system, the anodal electrodes will be positioned over the left DLPFC on the sites corresponding to F3, whereas the cathodal electrode will be placed above the right DLPFC, corresponding to F4. The electrode locations were verified using a computational brain model. All sessions will be conducted over five consecutive days (from Monday to Friday), with a 24-hour interval between sessions. Each participant will complete a total of 15 treatment sessions within a three-week period. Stimulation will be administered using the fixed parameters according to the established literature. For the active tDCS condition, a direct current of 2.0 mA will be applied (corresponding to a total charge of 2.4 C, a current density of 0.57 A/m2, and a charge density of 685.7 C/m2), for 20 minutes with ramp-up and ramp-down periods of 20 seconds each. For sham tDCS, the stimulation will utilize the same active tDCS arrangement, with an intensity of 2.0 mA. However, the current will be applied only for the 20 s ramp-up phase at the beginning and the 20 s ramp-down phase at the end of the stimulation. This protocol preserves blinding by mimicking the initial somatosensory sensations typically associated with active tDCS.
The selection of these parameters is grounded in prior evidence which demonstrates their functional specificity and efficacy in modulating cognitive processes in individuals diagnosed with schizophrenia.
All sessions will be conducted by trained personnel, and adverse events will be regularly monitored throughout the study.
Immediately after each tDCS stimulation, patients will undergo a 30-minute cognitive rehabilitation training session using the RehaCom computer system (HASOMED GmbH, Germany). Previous studies show that the time for which changes in neuronal excitability remain are proportional to the duration of stimulation and current used (Nitsche and Paulus, 2000). Based on these data, the authors assume that following a 20-minute tDCS session, the after-effects should last for at least 30 min (and hence the duration of neurocognitive training will be set at 30 min per session). The following programs will be used each week: day 1 (Monday), 3 (Wednesday) and 5 (Friday): EINK - shopping (different memory functions and selective attention), SUSA - selection of items (sustained attention), WOME - card games (working memory); day 2 (Tuesday) and 4 (Thursday): GEAU - maintaining the set vehicle speed (divided attention), LODE - creating logical sequences (logical reasoning); WOME - card games (working memory). During every session, each program will be applied for ten minutes, using a 17-inch laptop and a dedicated control panel. The following parameters will be set for SUSA: level up 85% and level down 70%; for LODE: upper threshold 90%, bottom threshold 60%, number of tasks per level 10; for WOME: number of tasks 10, repetitions 1, card display time 2000 ms; for GEAU: upper threshold 95%, bottom threshold 80%; for EINK: upper threshold 90%, bottom threshold 80%, repetitions 1, max time 90/300 s.
Participants will:
* Undergo assessments at three time points (V1 - baseline, V2 - after 3 weeks of intervention, V3 - after 8 weeks). * Be evaluated using CANTAB tests, the PANSS and CGI-S scales, and resting-state EEG.
The goal of the study is to determine whether applying tDCS before cognitive training improves executive function rehabilitation outcomes and supports the maintenance of these effects over time compared to cognitive training alone.
A vizsgálat 2 csoportja
- real tDCSMár használt kezelés, összehasonlításként
For the active tDCS condition, a direct current of 2.0 mA will be applied (corresponding to a total charge of 2.4 C, a current density of 0.57 A/m2, and a charge density of 685.7 C/m2), for 20 minutes with ramp-up and ramp-down periods of 20 seconds each.
Kezelés: active tDCS
- sham tDCSSzínlelt kezelés, összehasonlításként
For sham tDCS, the stimulation will utilize the same active tDCS arrangement, with an intensity of 2.0 mA. However, the current will be applied only for the 20 s ramp-up phase at the beginning and the 20 s ramp-down phase at the end of the stimulation. This protocol preserves blinding by mimicking the initial somatosensory sensations typically associated with active tDCS.
Kérdések a vizsgálat csapatának
- Milyen gyakran kell bejárnom, és egy-egy alkalom mennyi ideig tart?
- Megtérítik az utazási költséget?
- Megtarthatom a saját orvosomat?
- Mi történik, ha ki akarok lépni?
Contact the study team: see the registry record → Contacts and Locations
Oldal nyomtatása az orvosomnakAdatok és források
- Regiszteradat
- Szerepel a ClinicalTrials.gov-on.
- Hivatalos cím
- Evaluation of the Effects of Transcranial Direct Current Stimulation on the Effectiveness of Cognitive Function Rehabilitation Using the RehaCom System in Patients With Schizophrenia (Study Protocol)
- MI-összefoglaló
- A vizsgálat saját részvételi feltételeiből. Gépi kiolvasás: 2026. november 12.
- Illeszkedési kérdések
- Forrás: NCT07273175: ki vehet részt
- A regiszteradat frissítve
- 2026. január 13.