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临床试验/NCT07823218
NCT07823218尚未招募不适用

Longitudinal Effects of Brain Stimulation Techniques (ECT, TMS, VNS, taVNS) on Decision-Making and Reward Learning

Dr. Nils B. Kroemer1 个研究点 分布在 1 个国家目标入组 100 人开始时间: 2026年9月1日最近更新:
适应症

试验速览

阶段
不适用
状态
尚未招募
发起方
入组人数
100
试验地点
1
主要终点
Punishment learning rates

研究概览

简要总结

This study investigates the longitudinal effects of brain stimulation treatments on decision-making and reward learning. Here, we use daily assessments of reinforcement learning behavior in patients with depression who receive neuromodulation treatment to study potential associations between changes in decision-making and reward learning and changes in clinical symptoms.

详细描述

Brain stimulation techniques are increasingly applied to treat mental disorders, especially when psychotherapy and psychopharmacotherapy fail (Conroy & Holtzheimer, 2021). The efficacy of treating treatment-resistant depression has been demonstrated using electroconvulsive therapy (ECT; Espinoza & Kellern, 2022; Subramanian et al., 2022), transcranial magnetic stimulation (TMS, Trapp et al., 2025), and vagus nerve stimulation (VNS, Kamel et al., 2022). With regard to transcutaneous auricular vagus nerve stimulation (taVNS), a motivation-enhancing effect has been demonstrated in individuals with depression (Ferstl et al., 2024).

It is unclear to what extent these stimulation techniques also affect cognitive processes, such as learning and decision-making behavior, and whether such changes can explain treatment success. Temporary cognitive side effects, such as memory impairments, are known to occur with ECT treatments (Landry et al., 2021). Initial evidence regarding learning and decision-making behavior is available for taVNS, in which the vagal auricular branch is noninvasively stimulated at the ear. Acute taVNS stimulation at the left ear showed a reduced learning rate particularly during punishment (Kühnel et al., 2020), as well as increased reward sensitivity (Weber et al., 2021). Additionally, TMS over the left dorsolateral prefrontal cortex was shown to alter the ratio of reward-to-punishment learning rates (Biernacki et al., 2023). However, these initial findings on learning and decision-making behavior and the underlying computational parameters relate to acute stimulation. Long-term effects of brain stimulation techniques on theses processes, as used in routine clinical practice (e.g., eight TMS sessions or daily stimulation of the vagus nerve) remain unclear to date. Likewise, the influence of fluctuations in mental state, such as mood, on learning and decision-making behavior over the course of a treatment, as well as potential changes in this influence after successful treatment, remain mostly unexplored. However, a recent study found, that fluctuations in metabolic state affected reward sensitivity and punishment learning rates in obesity (Kühnel et al., 2025). In the context of effort-based decision-making, it has been shown that fluctuations in motivation influence reward sensitivity (Hewitt et al., 2025).

It is also not yet possible to say to what extent stimulation-induced changes in clinical symptoms are reflected in possible changes in decision-making and reward learning. However, increasing evidence of altered computational mechanisms in patients points towards this potential connection. For example, higher punishment learning rates were observed in individuals with depression (Pike & Robinson, 2022) and anhedonia was linked to reduced reward sensitivity (Huys & Browning, 2025). Also, greater temporal discounting of future rewards was observed in individuals with depression compared to those without a diagnosis (Amlung et al., 2019). An open question remains, that is whether, as symptoms improve, changes in cognitive processes also diminish.

Based on the above, the following objectives have been established: First, the acute and mid-term effects of the mentioned neurostimulation therapies on computational processes of decision-making and reward learning will be investigated over the course of a clinical application. We expect, that brain stimulation lowers punishment learning rates (Hypothesis 1). Subsequently, the effects of the various stimulation methods on punishment learning rates will be compared (acutely after stimulation as well as over the course of the treatment). In addition, the influence of state fluctuations, such as mood, on computational parameters of decision-making and reward learning, such as learning rates, will be modeled. We expect, that fluctuations in mood, motivation, and metabolic state are associated with changes in punishment learning rates (Hypothesis 2). Next, we investigate the effect of brain stimulation on working memory. We expect, that ECT impairs working memory compared to the other treatments (Hypothesis 3). Finally, we expect that changes in punishment learning rates predict changes in symptoms of depression, general well-being, and somatic symptoms (Hypothesis 4), as well as cognitive side effects on working memory (Hypothesis 5).

Here, we use daily assessments of reinforcement learning with a gamified online task (Neuser et al., 2023) over the course of 8 weeks to track longitudinal effects of brain stimulation on decision-making and reward learning in patients with depression who receive neuromodulation treatment (N = 100). Daily assessments are accompanied by an ecological momentary assessment (EMA) of mood and metabolic states. At least five runs of the reinforcement learning task should be played before the first stimulation as a baseline. Additionally, working memory (backward digit span task), depressive symptoms (BDI-II), well-being (WHO-5), and somatic symptoms (PHQ-15) are measured online at the start of the study before the first treatment, after 4 weeks, and after 8 weeks at the end of the study. Patients will be recruited directly from the clinic after brain stimulation treatment is indicated for them..

研究设计

研究类型
Observational
观察模型
Case Only
时间视角
Prospective

入排标准

年龄范围
18 Years 至 —(Adult, Older Adult)
性别
All
接受健康志愿者

入选标准

  • Indication for a brain stimulation treatment (ECT, TMS, VNS, taVNS) in the Department of Psychiatry and Psychotherapy at the University Hospital Bonn
  • Be able and willing to provide informed consent.

排除标准

  • Non-German speakers
  • Unclear ability to give consent to the study participation

研究组 & 干预措施

Electroconvulsive therapy (ECT)

Participants receive ECT as a treatment within the clinic. ECT intentionally causes a generalized seizure by passing electrical currents through the brain under anesthesia. The treatment protocol (e.g., number of treatments) is independent of study participation and follows the doctor's orders. Participants are enrolled after the treatment indication is confirmed.

Transcranial magnetic stimulation (TMS)

Participants receive TMS as a treatment within the clinic. TMS is a non-invasive procedure in which a magnetic coil is used to induce electrical currents in the brain and thus influence cortex activity. The treatment protocol (e.g., number of treatments, type of TMS) is independent of study participation and follows the doctor's orders. Participants are enrolled after the treatment indication is confirmed.

invasive vagus nerve stimulation (VNS)

Participants receive VNS as a treatment within the clinic. VNS is a surgical treatment in which a stimulation device is implanted that sends electrical impulses to the vagus nerve. The treatment protocol (e.g., stimulation settings) is independent of study participation and follows the doctor's orders. Participants are enrolled after the treatment indication is confirmed.

transcutaneous vagus nerve stimulation (tVNS)

Participants receive tVNS as a treatment from the clinic for at home stimulation. To stimulate vagal afferents, the electrode will be placed at the cymba conchae of the right ear using a previously established conventional stimulation protocol (30s ON, 30s OFF; tVNS E device, tVNS Technologies GmbH, Erlangen, Germany). The stimulation can be applied for up to 4h per day and participants self-select stimulation time and duration based on the doctor's orders. Participants are enrolled after the treatment indication is confirmed.

Control

Participants receive an indication for a stimulation treatment within the clinic, but do not make use of it. Participants are included after treatment indication.

结局指标

主要结局

Punishment learning rates

时间窗: Assessed online up to 5 times before the first stimulation treatment and daily throughout the study (8 weeks).

The primary outcome are punishment learning rate estimates from a computational reinforcement learning model. Learning rates will be compared within and between stimulation conditions. Reinforcement learning is repeatedly measured with a bandit task with fluctuating reward probabilities (reward learning task). Reward learning behavior will be collected online over up to 60 runs, each including 150 trials.

次要结局

  • Stimulation-induced mid-term changes in the backward digit span(Assessed before the first stimulation treatment and after 4 and 8 weeks (10 minutes).)
  • Correct choices in the reward learning task(Assessed online at least 5 times before the first stimulation treatment and daily throughout the study (8 weeks).)
  • Reward sensitivity(Assessed online at least 5 times before the first stimulation treatment and daily throughout the study (8 weeks).)
  • Weighting of learned values and rewards at stake (lambda)(Assessed online at least 5 times before the first stimulation treatment and daily throughout the study (8 weeks).)
  • Stimulation-induced mid-term changes in reward learning rates(Assessed online at least 5 times before the first stimulation treatment and daily throughout the study (8 weeks).)
  • Association between mood state and punishment learning rates(Assessed online at least 5 times before the first stimulation treatment and daily throughout the study (8 weeks).)
  • Association between metabolic state and punishment learning rates(Assessed online at least 5 times before the first stimulation treatment and daily throughout the study (8 weeks).)
  • Association between changes in punishment learning rates and changes in depressive symptoms(Depressive symptoms are assessed before the first stimulation treatment and after 4 and 8 weeks. Reward learning is assessed online at least 5 times before the first stimulation treatment and daily throughout the study (8 weeks).)
  • Association between motivational state and punishment learning rates(Assessed online at least 5 times before the first stimulation treatment and daily throughout the study (8 weeks).)
  • Association between changes in punishment learning rates and changes in mental well-being(Mental well being is assessed before the first stimulation treatment and after 4 and 8 weeks. Reward learning is assessed online at least 5 times before the first stimulation treatment and daily throughout the study (8 weeks).)
  • Association between changes in punishment learning rates and changes in somatic symptoms(Somatic symptoms are assessed before the first stimulation treatment and after 4 and 8 weeks. Reward learning is assessed online at least 5 times before the first stimulation treatment and daily throughout the study (8 weeks).)
  • Association between changes in the backward digit span and changes in punishment learning rates(Assessed online at least 5 times before the first stimulation treatment and daily throughout the study (8 weeks).)
  • Response times in the reward learning task(Assessed online at least 5 times before the first stimulation treatment and daily throughout the study (8 weeks).)
  • Backward digit span(Assessed before the first stimulation treatment and after 4 and 8 weeks (10 minutes).)
  • BDI-II (Beck Depression Inventory-II)(Assessed before the first stimulation treatment and after 4 and 8 weeks (10 minutes).)
  • WHO-5 (World Health Organization-Five Well-Being Index)(Assessed before the first stimulation treatment and after 4 and 8 weeks (3 minutes).)
  • PHQ-15 (Patient Health Questionnaire-15)(Assessed before the first stimulation treatment and after 4 and 8 weeks (5 minutes).)

研究者

发起方
Dr. Nils B. Kroemer
申办方类型
Other
责任方
Sponsor Investigator
主要研究者

Dr. Nils B. Kroemer

Prof. Dr. rer. nat.

University of Bonn

研究点 (1)

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