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Funding Opportunity




  Not Verified

Advancing innovative interventions for mental, behavioural and neurodevelopmental disorders

European Commission

Expected Outcome:

This topic aims at supporting activities that are enabling or contributing to one or several expected impacts of destination “Tackling diseases and reducing disease burden”. To that end, proposals under this topic should aim to deliver results that are directed, tailored towards and contributing to all the following expected outcomes:

  • The scientific and clinical communities make effective use of state-of-the-art knowledge, data, technologies, tools, methods, best practices, and trainings to underpin and complement the development of innovative interventions[1] aimed at achieving a lasting benefit.
  • The scientific and clinical communities benefit from the exchange of data, knowledge and best practices, thereby strengthening their collaboration in the EU, the Associated Countries and beyond.
  • The scientific and clinical communities make wide use of relevant databases and/or integrate them with existing infrastructures for storage and sharing of collected data according to FAIR[2] principles, thereby encouraging further use of the data.
  • Policymakers, funders, scientific and clinical communities, patient organisations, regulators, and other relevant bodies are informed of the research advances made and the requirements for a widespread implementation of the innovative therapeutic interventions and complementary approaches.
  • Patients and caregivers are constructively engaged with the research, ensuring that their needs are catered for, with the aim of tangibly benefitting from the interventions.

Scope:

Mental, behavioural and neurodevelopmental disorders, that include for example severe depression, anxiety, schizophrenia, psychosis, post-traumatic stress disorder (PTSD), addictive behaviours (drugs[3], alcohol, gaming and others), obsessive-compulsive disorder, eating disorders and autism spectrum disorder are a high burden for patients, health systems and society, and remain unmet medical needs. More innovative, safer and more effective therapeutic and relapse-preventing solutions based on active substances are required, as for example for mental disorders many available treatments show modest efficacy, non-negligible side effects, discontinuation problems and high relapse rates. Additionally, other non-invasive multidisciplinary and/or transdiagnostic approaches (e.g. neurostimulation, neuroimaging, digital, non-pharmaceutical, psychotherapy, psychosocial) should be further developed to complement the therapeutic and relapse prevention solutions. These approaches aim to further improve health outcomes, self-determination, autonomy and quality of life in the long-term.

The disorders within the scope of this topic fall under Chapter 6 of the International Classification of Diseases[4]. Rare diseases are excluded[5].

Proposals should address most of the following aspects:

  • Perform rigorous clinical studies into the safety and efficacy of the innovative interventions and their mode of administration, ensuring adequate cohorts/sample sizes with adequate representation of the patient population, including in terms of age, sex and ethnicity.
  • Through the clinical studies, gain further insight into the mechanism(s) of action of the innovative therapies and complementary approaches. This could entail analyses of imaging (e.g. MRI, ultrasound, nuclear imaging), as well as physiological, molecular, biochemical or omics signatures revealing potential perturbations prior to the intervention and recovery thereafter, and it could lead to the development of surrogate endpoints. This insight should open the path to more personalised interventions and approaches.
  • Use and/or develop technologies, including digital ones (e.g., (generative) Artificial Intelligence - AI[6], wearable technologies) to help implement and monitor the long-term efficacy of the intervention(s), as well as manage the disorder and/or monitor their progression (e.g. with unobtrusive technologies suitable for patient monitoring at home and in real-world conditions), whilst also ensuring they are bias-free, inclusive, and ethically sound.
  • Exploit existing data, biobanks, registries and/or cohorts, together with the generation of new data that should be managed in line with the FAIR principles.
  • Engage all relevant stakeholders (especially patients and patients’ representatives for the disorder, caregivers, clinicians, counsellors, regulators, etc.) to design end-user optimised interventions, applying gender-sensitive and intersectional approaches.
  • Advance research by leveraging already existing and emerging state-of-the-art research infrastructures (e.g. ECRIN[7], EATRIS[8], EBRAINS[9], BBMRI[10], EuroBioImaging[11], European Genomic Data Infrastructure[12], etc.), as well as results stemming from EU-supported research projects, where applicable.
  • Engage with national public health authorities and regulators to ensure a robust development pathway and further uptake of the intervention.

The participation of start-ups, micro, small and medium-sized enterprises (SMEs)[13] is encouraged with the aim of strengthening their scientific and technological foundations, enhancing their innovation potential, and exploring possibilities for commercial exploitation.

Funded projects should liaise with the European Partnership for Brain Health (covered by topic HORIZON-HLTH-2025-02-DISEASE-01) once launched.

The topic requires the effective contribution of social sciences and humanities (SSH) disciplines and the involvement of SSH experts, institutions as well as the inclusion of relevant SSH expertise, in order to produce meaningful and significant effects enhancing the societal impact of the related research activities.

All projects funded under this topic are strongly encouraged to participate in networking and joint activities, as appropriate. Therefore, proposals should include a budget for the attendance to regular joint meetings and may consider covering the costs of any other potential joint activities without the prerequisite to detail concrete joint activities at this stage. The details of these joint activities will be defined during the grant agreement preparation phase.

Applicants invited to the second stage should provide details of their clinical studies[14] in the dedicated annex using the template provided in the submission system. As proposals under this topic are expected to include clinical studies, the use of the template is strongly encouraged.

AI Based Application Success Predictor

1️⃣ Strong, Mission-Aligned Impact (Most Important Across EC Calls)

The EC is impact-driven: proposals must show how the project will:

Solve a major European or global societal challenge

Deliver measurable, lasting benefits for EU citizens

Produce outputs that can be used by policymakers, industry, or society

Align with Horizon Europe missions, priorities, and strategic agendas

Predictor: Clear, quantifiable, EU-level impact → strongest scoring factor.

2️⃣ Clear, Ambitious, but Achievable Objectives

Successful proposals show:

2–4 well-defined objectives linked to the Work Programme call text

Clearly articulated research questions or innovation goals

Logical, realistic expected outcomes and deliverables

Feasible scientific and technical approaches

Predictor: Balanced ambition + feasibility.

3️⃣ Excellent, Cutting-Edge Science or Innovation

For RIA/IA/CSA or ERC-level grants, reviewers expect:

High novelty and innovation

Strong grounding in current state-of-the-art

Clear advancement beyond existing approaches

Solid theoretical or experimental foundations

Robust methodological design

Predictor: Scientific excellence is essential for competitive scoring.

4️⃣ Strong Consortium with Complementary Expertise

EC proposals are consortium-driven (except ERC/EIC Accelerator).

High-scoring consortia:

Cover all needed competencies (science, industry, policy, ethics, dissemination)

Include SMEs, industry partners, NGOs, and public bodies when relevant

Are geographically diverse across EU Member States and Associated Countries

Demonstrate strong leadership and communication structures

Predictor: Well-constructed consortium with clear roles.

5️⃣ Clear Pathway From Outputs → Outcomes → Impact

Evaluators look for a credible trajectory showing:

How research leads to specific outputs (data, tools, prototypes)

How outputs lead to uptake or use

How use produces societal, economic, scientific, or policy impact

Strong Key Performance Indicators (KPIs) and impact metrics

Predictor: Clearly mapped impact pathway.

6️⃣ Strong Implementation Plan (Work Packages, Deliverables, Gantt Chart)

Winning proposals have:

Well-designed Work Packages (WPs) with clear scope and responsibilities

Interdependencies identified and risk-mitigation strategies

Detailed milestones and deliverables

Feasible budget aligned with tasks

Strong project management plan

Predictor: High implementation quality boosts the “Excellence” and “Implementation” scores.

7️⃣ Policy Relevance and Contribution to EU Strategies

Especially critical for health, climate, digital, and social calls.

Proposals score higher when they link to:

EU Cancer Mission

EU Green Deal

Digital Europe strategy

EU Biodiversity Strategy

EU Health Union & One Health

Open Science & FAIR data mandates

Predictor: Clear alignment with EU policies.

8️⃣ Strong Stakeholder & Citizen Engagement (Especially in Social & Health Missions)

EC values inclusivity:

Patient groups

Civil society organizations

Public sector bodies

Regulatory agencies

Citizen science components

Stakeholder letters of intent or commitment strengthen credibility.

Predictor: Engagement adds impact and relevance.

9️⃣ Robust Data Management, Open Science, and Ethics

Mandatory components include:

FAIR Data Management Plan

Open access publications

Ethics self-assessment

GDPR compliance

Data security, governance, and ethical approvals

Animal-use reduction and justification (if applicable)

Predictor: Clear compliance with ethical and data obligations.

10️⃣ Well-Justified Budget and Resource Allocation

Budget must be:

Proportional to tasks

Transparent and reasonable

Efficiently distributed among partners

Free from padding or unjustified costs

Predictor: Realistic budgets improve Implementation scores.

🚫 COMMON PITFALLS THAT LEAD TO EC GRANT REJECTION

PitfallWhy It Fails
Weak connection to Work Programme textImmediate score reduction
Vague or generic impact statementsPoor Impact score
Overly ambitious, unrealistic scopeFeasibility concerns
Poorly structured consortiumLow Implementation score
No policy relevanceWeak strategic alignment
Lack of concrete KPIs or outcomesImpact unclear
Weak data or ethics planEligibility/score penalties
No exploitation or dissemination planInsufficient impact credibility
Budget misalignmentReviewer distrust

Eligible Countries

Eligible Countries are described in Annex B of the Work Programme General Annexes.

A number of non-EU/non-Associated Countries that are not automatically eligible for funding have made specific provisions for making funding available for their participants in Horizon Europe projects. See the information in the Horizon Europe Programme Guide.

Other Eligible Conditions

In recognition of the opening of the US National Institutes of Health’s programmes to European researchers, any legal entity established in the United States of America is eligible to receive Union funding.

If projects use satellite-based earth observation, positioning, navigation and/or related timing data and services, beneficiaries must make use of Copernicus and/or Galileo/EGNOS (other data and services may additionally be used).

The following exceptions apply: subject to restrictions for the protection of European communication networks.

Sponsor Institute/Organizations: European Commission

Sponsor Type: Corporate/Non-Profit

Address: Rue de la Loi 200 / Wetstraat 200, 1049 Brussels, Belgium.

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Grant

Letter Of Intent Deadline:

Apr 16, 2026

Final Deadline:

Apr 16, 2026

Funding Amount:

$9,440,000

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