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Effect of TMS Treatment on Defense Mechanisms and Functionality in Patients With Depression

7. oktober 2026 opdateret af: Kardelen Erdoğan, Namik Kemal University

The Effect of Transcranial Magnetic Stimulation (TMS) Treatment on Defense Mechanisms and Functionality in Patients With Depression

This prospective observational study aims to evaluate changes in psychological defense mechanisms in patients with non-psychotic major depressive disorder (MDD) undergoing repetitive Transcranial Magnetic Stimulation (rTMS) therapy. The study investigates whether rTMS induces a shift from immature to more mature defense mechanisms and assesses how these changes relate to improvements in depressive symptom severity, anxiety levels, and overall functionality at baseline, 1-month, and 3-month follow-ups.

Studieoversigt

Status

Ikke rekrutterer endnu

Detaljeret beskrivelse

Major depressive disorder (MDD) significantly impacts mood, cognitive function, and psychological defense structures. While repetitive Transcranial Magnetic Stimulation (rTMS) is an established non-invasive neuromodulation therapy for depression, its influence on psychodynamic constructs such as defense mechanisms remains insufficiently explored.

This single-center prospective study will enroll 50 adult participants (aged 18-65) diagnosed with non-psychotic MDD according to DSM-5 criteria (confirmed via SCID-5). Participants will receive rTMS treatment as part of their standard clinical care. Clinical assessments will be conducted by a blinded researcher at three time points: baseline (pre-treatment), 1 month, and 3 months post-baseline.

Primary outcomes will measure shifts in defense mechanism styles (mature, neurotic, immature) using the Defense Style Questionnaire (DSQ). Secondary outcomes will assess depressive symptom severity (Hamilton Depression Rating Scale - HAM-D), anxiety levels (Hamilton Anxiety Rating Scale - HAM-A), clinical severity and improvement (Clinical Global Impression Scale - CGI), and functional impairment (World Health Organization Disability Assessment Schedule 2.0 - WHODAS 2.0).

Undersøgelsestype

Observationel

Tilmelding (Anslået)

50

Kontakter og lokationer

Dette afsnit indeholder kontaktoplysninger for dem, der udfører undersøgelsen, og oplysninger om, hvor denne undersøgelse udføres.

Studiekontakt

Studiesteder

      • Tekirdağ, Tyrkiet (Türkiye)
        • Tekirdağ Namik Kemal University Faculty of Medicine, Department of Psychiatry
        • Kontakt:

Deltagelseskriterier

Forskere leder efter personer, der passer til en bestemt beskrivelse, kaldet berettigelseskriterier. Nogle eksempler på disse kriterier er en persons generelle helbredstilstand eller tidligere behandlinger.

Berettigelseskriterier

Aldre berettiget til at studere

18 år til 65 år (Voksen, Ældre voksen)

Tager imod sunde frivillige

Ingen

Køn, der er berettiget til at studere

Alle

Prøveudtagningsmetode

Ikke-sandsynlighedsprøve

Studiebefolkning

Adults aged 18-65 years with non-psychotic major depressive disorder (MDD) who are evaluated for suitability for transcranial magnetic stimulation (TMS) treatment at the Psychiatry Clinic/TMS Unit of Tekirdağ Namık Kemal University Hospital. The diagnosis of MDD will be confirmed using the Structured Clinical Interview for DSM Disorders (SCID). Approximately 50 participants who meet the eligibility criteria and provide written informed consent will be included.

Beskrivelse

Inclusion Criteria:

  • Age between 18 and 65 years
  • Diagnosis of major depressive disorder without psychotic features according to DSM-5 criteria
  • Confirmation of diagnosis via SCID
  • Major depressive disorder as the primary reason for admission
  • Willingness to participate and signing the written informed consent form

Exclusion Criteria:

  • Presence of contraindications for TMS (e.g., metallic implants)
  • Known active psychotic symptoms
  • History of TMS treatment in the past 3 months
  • Presence of known organic brain syndrome, neurological, or major systemic medical conditions
  • Presence of known intellectual disability or significant cognitive impairment
  • Active substance or alcohol use disorder
  • Illiteracy

Studieplan

Dette afsnit indeholder detaljer om studieplanen, herunder hvordan undersøgelsen er designet, og hvad undersøgelsen måler.

Hvordan er undersøgelsen tilrettelagt?

Design detaljer

  • Observationsmodeller: COHORT
  • Tidsperspektiver: PROSPECTIVE

Kohorter og interventioner

Gruppe / kohorte
TMS Treatment Group

Patients diagnosed with major depressive disorder receiving Transcranial Magnetic Stimulation therapy.

Hvad måler undersøgelsen?

Primære resultatmål

Resultatmål
Foranstaltningsbeskrivelse
Tidsramme
Change in Defense Mechanisms (Defense Style Questionnaire - DSQ)
Tidsramme: Baseline, 1 month, and 3 months

Evaluates shifts in mature, neurotic, and immature psychological defense mechanism styles in patients with major depressive disorder following TMS treatment.

Baseline, 1 month, and 3 months

Sekundære resultatmål

Resultatmål
Foranstaltningsbeskrivelse
Tidsramme
Change in Anxiety Symptom Severity (Hamilton Anxiety Rating Scale - HAM-A)
Tidsramme: Baseline, 1 month and 3 months

Assesses psychic and somatic anxiety symptom severity.

Baseline, 1 month and 3 months
Change in Depressive Symptom Severity (Hamilton Depression Rating Scale - HAM-D)
Tidsramme: Baseline, 1 month, and 3 months

Assesses the severity of depressive symptoms

Baseline, 1 month, and 3 months
Change in Clinical Global Impression (CGI)
Tidsramme: Baseline, 1 month, and 3 months

Measures overall illness severity and clinical improvement.

Baseline, 1 month, and 3 months
Change in Disability and Functionality (World Health Organization Disability Assessment Schedule 2.0 - WHODAS 2.0)
Tidsramme: Baseline, 1 month, and 3 months

Evaluates level of functional disability across six domains (understanding/communicating, mobility, self-care, getting along, life activities, participation).

Baseline, 1 month, and 3 months

Samarbejdspartnere og efterforskere

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Datoer for undersøgelser

Disse datoer sporer fremskridtene for indsendelser af undersøgelsesrekord og resumeresultater til ClinicalTrials.gov. Studieregistreringer og rapporterede resultater gennemgås af National Library of Medicine (NLM) for at sikre, at de opfylder specifikke kvalitetskontrolstandarder, før de offentliggøres på den offentlige hjemmeside.

Studer store datoer

Studiestart (Anslået)

1. oktober 2026

Primær færdiggørelse (Anslået)

1. april 2027

Studieafslutning (Anslået)

1. juli 2027

Datoer for studieregistrering

Først indsendt

27. september 2026

Først indsendt, der opfyldte QC-kriterier

27. september 2026

Først opslået (Faktiske)

2. oktober 2026

Opdateringer af undersøgelsesjournaler

Sidste opdatering sendt (Faktiske)

13. oktober 2026

Sidste opdatering indsendt, der opfyldte kvalitetskontrolkriterier

7. oktober 2026

Sidst verificeret

1. oktober 2026

Mere information

Begreber relateret til denne undersøgelse

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