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NCT Number: NCT07284238

Suicidal Ideation Framework: Grounded Theory Study, Catalonia

This doctoral project aims to develop a comprehensive theoretical model of the process through which the suicidal ideation framework is configured as a symbolic, narrative, and relational expression, adopting a multiperspective approach that spans the suicide attempt and the stages of care and recovery. Moving away from biomedical reductionisms, this investigation seeks to identify shared meaning-making nuclei and discursive fractures that reflect the inherent conflictuality of the suicidal act.

Grounded in the integration of the theoretical frameworks previously outlined, this study adopts an interpretive-constructivist approach. Phase 1 will include studies conducted in OECD countries, providing a broad and conceptually diverse interpretive foundation. Phase 2, conducted in Catalonia, will deepen situated configurations, assuming that local sociocultural frameworks act as interpretive prisms for globally relevant phenomena.

Overall, this theoretical-methodological architecture not only ensures conceptual robustness and coherence, but also articulates an ethical and epistemic commitment to understanding suicide through the complexity of its human textures. By centering suffering, listening to historically silenced voices, honoring the singularity of each life trajectory, and grounding the inquiry in an ethics of care, this study aims to transcend a merely technical-instrumental logic of knowledge.

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Key information

Age range

18 year and older

Sex eligibility

All sexes

Study type

Observational

Primary location

Hospital de la Santa Creu i Sant Pau

Barcelona, 08041, Spain

Location contact

David Giménez Díez, RN, MSc, PhD

SUB_INVESTIGATOR

Ismael Parrilla Ríos, RN, MSc

SUB_INVESTIGATOR

Juan-Manuel Leyva Moral, RN, MSc, PhD

SUB_INVESTIGATOR

Mónica Romero Pastor, RN, MSc, PhD

SUB_INVESTIGATOR

Sergio de la Hera Herrero RN, MSc, DS, Bachelor of Science in Nursing

CONTACT

[email protected]

+34935537661

About this study

Initial Analytical Premises:

It is posited that the suicidal ideation framework constitutes a symbolic, relational, dynamic, and multiperspective configuration whose emergence cannot be understood apart from the narrative, contextual, and structural arrangements mediating experiences of exclusion, hopelessness, affective disconnection, loss of vital meaning, and extreme suffering.

From this standpoint, a foundational premise is established: the suicidal ideation framework cannot be conceived as a static, universal, or univocal category. Rather, it is shaped as a constellation of meanings and signifiers in tension, woven through the interaction of ambivalences, silences, contradictions, and narrative ruptures. Such configuration emerges from complex subjective processes marked by structural inequalities, social stigma, institutional vulnerability, or care models that often render distress invisible or reduce it to pathologizing categories.

It is therefore assumed that an in-depth understanding of lived experiences attributed to the configuration process of the suicidal ideation framework-through the semiotic complexity of each perspective involved-will not only allow the identification of narrative structures and shared meaning nodes, but also help unravel discursive fractures that reflect the inherent conflictuality of the voluntary death process as a response to suffering experienced as intolerable.

Research Question:

From the perspective of individuals who have attempted suicide, members of their support networks, and healthcare professionals involved in their care-within the mental health services of the autonomous community of Catalonia, and informed by qualitative evidence from OECD countries-how is the suicidal ideation framework configured as a symbolic, narrative, and relational expression, based on the lived experiences attributed by these actors in the sociocultural and healthcare settings where they interact throughout the period encompassing the suicide attempt and the subsequent stages of care and recovery?

General Study Design:

The methodological design unfolds across two sequential and complementary phases:

  • Phase 1 will adopt a qualitative systematic review methodology, using an interpretive qualitative metasynthesis design (Sandelowski & Barroso). It will integrate findings from previous qualitative and mixed-methods studies through reflexive thematic analysis (Braun & Clarke), supported by ATLAS.ti CAQDAS software. The process will follow PRISMA 2020, ENTREQ, and COREQ guidelines, selecting literature with high methodological quality (≥9/10 criteria of the JBI tool). The bibliographic search will be conducted across five international databases (PubMed, CINAHL, PsycINFO, Scopus, WoS), and screening will be performed by pairs of reviewers seeking ≥95% agreement and a Cohen's Kappa ≥0.80 to ensure inter-rater reliability.
  • Phase 2 will follow an inductive qualitative methodology using a constructivist grounded theory design (Charmaz), framed within the interpretive paradigm under a relativist ontology and a subjectivist epistemology. The study population will be structured into three complementary analytical groups: (a) Individuals who have made one or more suicide attempts in the 6 months-3 years prior to the interview; (b) Members of support networks (family, friends, community); and (c) Healthcare professionals directly involved in the care of individuals who have attempted suicide. Participant recruitment will be coordinated with mental-health professionals following principles of autonomy, non-maleficence, and dignity protection. Institutional agreements will support safe referrals. Sample size will be determined by theoretical saturation. Theoretical-evolutionary sampling will be employed, and data generation techniques will include in-depth individual interviews (30-45 min) and discussion groups (4-6 participants, 60-90 min). Sessions will be conducted in authorised hospital or community settings, with an observer noting field data. Qualitative material, collected through audio recording, will undergo inductive-interpretive qualitative content analysis informed by constructivist grounded theory: initial coding, focused coding, and theoretical integration. An abductive logic will guide movement between data and conceptualisation. Constant comparison, analytic memos, conceptual diagrams, and conditional matrices will ensure rigour. Triangulation, participant-involvement workshops, and external audit will strengthen quality. ATLAS.ti will support systematic data management. Data handling will follow the Declaration of Helsinki and GDPR. The PI is responsible for database creation and integrity.

Phase 1 Biases and Limitations:

Publication bias: mitigated through inclusion of qualitative systematic reviews and critical heterogeneity analysis.

Language limitation: mitigated through inclusion of multicentric studies and triangulation with technical/institutional reports.

Phase 2 Biases and Limitations:

Researcher bias: mitigated through reflexivity, peer review, constant comparison, and participant validation.

Selection bias: mitigated through diverse theoretical sampling and safe inclusion of vulnerable profiles.

Participant response bias: mitigated through emotionally safe environments, rapport, neutral questioning, and professional accompaniment when needed.

Quality Control:

The PI will ensure accuracy and consistency in the Case Report Forms, maintain documentation for ≥10 years, and provide access to monitors, auditors, ethics committees, and regulatory authorities upon request.

Conclusion:

This innovative interpretive contribution represents an ethical commitment to restoring the agency of the actors involved. Ultimately, this research proposal acknowledges the role of the nursing profession as an operative agent of change and as a privileged epistemic subject in confronting one of the most complex and silenced phenomena of contemporary human experience.

Who can participate

Healthy volunteers accepted: No

Only the study team can determine whether someone qualifies for participation.

Inclusion criteria

  • Adults ≥18 years of age.
  • Usual residence in Catalonia (Spain).
  • Ability to understand, speak, read, and write in Catalan or Spanish.
  • Belonging to one of the three defined analytical groups:

(A) Individuals who have attempted suicide within the past 6 months to 3 years. (B) Members of their family, social, or community support networks. (C) Healthcare professionals directly involved in the care of individuals who have attempted suicide.

  • Demonstrated clinical/emotional stability ensuring safe participation, as confirmed by the referring clinician.
  • For individuals with lived experience (Group A): at least 6 months since the last suicide attempt or acute clinical crisis.
  • For support networks (Group B): having maintained meaningful proximity or involvement during or after the suicide attempt.
  • For healthcare professionals (Group C): minimum of 1 year of professional experience in mental health care.

Exclusion criteria

  • Presence of acute clinical decompensation preventing safe participation.
  • Active suicidal risk or acute crisis at the time of recruitment.
  • Acute vulnerability identified during screening.
  • Inability to provide informed consent.
  • Direct hierarchical dependence or conflict of interest with the research team (for Group C).

Treatment and study plan

In-Depth Qualitative Interview

Procedure

In-depth interviews aimed at exploring participants' lived experiences, meaning-making processes, and contextual factors related to the configuration of the suicidal ideation framework. Interviews will last approximately 30-45 minutes and will be conducted by the Principal Investigator in a confidential, safe, and clinically monitored setting. No clinical treatment or diagnostic procedure is administered.

Discussion Group

Procedure

Non-directive discussion groups composed of 4-6 participants from the same analytic category (suicide attempt survivors, support network members, or healthcare professionals). Sessions will last 60-90 minutes and will facilitate the collective exploration of relational, contextual, and sociocultural dynamics associated with the suicidal ideation framework. The procedure is solely qualitative and involves no therapeutic intervention or clinical manipulation.

Primary outcomes

  1. Conceptual Synthesis of Qualitative Findings.

    Time frame: Through Phase 1 completion, an average of 12-18 months.

    Generation of a third-order conceptual synthesis integrating first- and second-order findings from qualitative and mixed-methods studies conducted in OECD countries. This synthesis will be developed through reflexive thematic analysis and will provide a high-order interpretative framework that will:

    • consolidate cross-contextual patterns and divergences in experiences attributed to suicide.
    • inform the initial theoretical orientation of Phase 2.
    • guide purposive and theoretical sampling.
    • support the development of initial coding strategies in the constructivist grounded theory phase.

    Measure Type: Qualitative interpretative meta-synthesis conceptual output.

  2. Emergent Theoretical Model.

    Time frame: Through study completion, an average of 24-30 months.

    Qualitative identification, comparative analysis and inductive-interpretive integration of the main categories, subcategories and theoretical relationships that explain how the suicidal ideation framework is configured as a symbolic, narrative and relational phenomenon. This outcome captures the core theoretical structure produced through initial coding, focused coding and theoretical integration, derived from the constructivist grounded theory analysis of interviews and discussion groups.

    Measure Type: Qualitative conceptual model (Grounded Theory).

Secondary outcomes

  1. Identified Narrative Structures and Meaning-Making Patterns.

    Time frame: Through study completion, an average of 24-30 months.

    Qualitative identification of narrative structures, ambivalences, silences, contradictions and discursive ruptures attributed by participants to the process of configuring the suicidal ideation framework, across the three analytic groups (individuals with suicide attempt history, members of support networks, healthcare professionals).

    Measure Type: Qualitative thematic patterns (Reflexive Thematic Analysis).

  2. Influence of Socio-cultural and Biographical Factors.

    Time frame: Through study completion, an average of 24-30 months.

    Inductive analysis of how socioaffective bonds, sociocultural frames, structural inequalities and biographical trajectories shape and modulate the subjective and relational processes involved in the configuration of the suicidal ideation framework.

    Measure Type: Qualitative thematic and relational patterns.

  3. Relational and Contextual Mechanisms.

    Time frame: Through study completion, an average of 24-30 months.

    Examination of how relational dynamics, contextual interactions and social environments contribute to modelling the configuration of the suicidal ideation framework across different participant groups.

    Measure Type: Qualitative category development.

  4. Perceived Barriers and Facilitators in Healthcare.

    Time frame: Through study completion, an average of 24-30 months.

    Identification of perceived barriers, facilitators, protective factors and contextual conditions present in mental health and emergency care settings, as described by individuals with suicide attempt history, their support networks and healthcare professionals.

    Measure Type: Qualitative thematic analysis.

Study contacts

Contact information is provided by the study sponsor or research team.

Sergio de la Hera Herrero RN, MSc, DS, Bachelor of Science in Nursing

CONTACT

[email protected]

+34689239358

Sponsors and collaborators

Lead sponsor

Fundació Institut de Recerca de l'Hospital de la Santa Creu i Sant Pau

Other

Registry information

Official study title

Process of Configuring the Suicidal Ideation Framework: A Grounded Theory Study in Catalonia, Spain

Acronym: SUIF-GT-CAT

Important dates

Study start
2026
Primary completion
2027
Study completion
2027
First posted
Dec 16, 2025
Registry last updated
Dec 16, 2025

OpenTrials presents study information sourced from ClinicalTrials.gov. The official registry record should be consulted for the latest information.

View the official ClinicalTrials.gov record (opens in a new tab)

This listing is for discovery and informational purposes only. It is not medical advice, does not guarantee that a study is recruiting, and does not determine eligibility. Contact the study team and a qualified healthcare professional when considering participation.

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