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NCT Number: NCT05435222

Evaluation of a Male-specific Psychotherapeutic Program for Major Depressive Disorders

This project aims to evaluate a male-specific psychotherapeutic program (MSPP) for MDD based on cognitive behavioral therapy (CBT). The primary goal is to test the superiority of the MSPP. This will be conducted in two groups of depressed men, namely eudonadal depressed men and hypogonadal depressed men receiving testosterone treatment (TT). In a randomized study design, the MSPP will be compared to a standard CBT and a waitlist control group, resulting in a total of six study groups. Both standardized psychotherapy programs will encompass 18 sessions delivered in a weekly manner, starting at study week 6 and continuing until study week 24. Aligned with the TT-related medical visits of the hypogonadal men, all participants will be followed up with clinical assessments and biosampling at weeks 0, 6, 15, 24, 36. In addition, a separate healthy control group will be examined, which will undergo only baseline assessments.

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Key information

Age range

25 year–50 year

Sex eligibility

Male

Study type

Interventional

Phase

Not applicable

Primary location

About this study

Background: Although women are twice as likely to suffer from major depressive disorder (MDD) than men, there are still over 100 million men affected by this condition worldwide. Unfortunately, men suffering from MDD seek mental health services about 30% less than women, leaving a large portion of men with unresolved mental health needs. This is reflected in 2-fold higher rates of alcohol use disorder and 4-fold higher rates of completed suicide amongst men, while MDD is considered a prime risk factor for both. A case is made for male-typical MDD phenotypes with differing symptom presentation often unrecognized by clinicians. Although cognitive behavioral therapy (CBT) represents an effective treatment for MDD, conformity to traditional masculinity norms based on stoicism, self-reliance, and restrictive emotionality often hinder men from engaging in psychotherapy. Therefore, a need to address this diagnostic and treatment gap emerges, while recent studies have identified a lack of male-specific psychotherapeutic programs (MSPP) that could persuade more men to take on psychotherapy based on a male-tailored nature, focusing on male-specific topics and being introduced in male-typical environments.

Method and study procedures: In total, 144 depressed men aged between 25 and 50 will be recruited. After Screening procedures, included participants are stratified by testosterone status (hypogoadal vs. eugonadal) and randomized to one of the conditions: MSPP, CBT, Waitlist. This results in six intervention groups (MSPP, CBT, Waitlist, MSPP+TT, CBT+TT, Waitlist+TT). Hypogonadal men will receive testosterone treatment administered at the Andrology-Urology Center (Uroviva). MSPP and CBT intervention groups will receive weekly therapy sessions for MDD over 18 weeks. All participants will be invited to a total of five examination appointments (weeks 0, 6, 15, 24, 36) at the psychological institute of the university of Zurich. In addition, a separate healthy control group will be examined, which will undergo only baseline assessments.

Expected results: Compared to the waitlist control groups, the treatment groups are expected to be more effective and efficacious (depression score reduction of ≥50%) at week 24 and at follow-up week 36. The MSPP, compared to CBT, is expected to show higher effectiveness and efficacy for depression symptoms, higher acceptability and a greater reduction of gender role conflict. In addition, it is expected that the initially hypogonadal men will have increased symptom improvement due to TT as compared to the eugonadal men in the parallel groups and that TT receiving men show an adjunct effect of added psychotherapy as compared to men in the waitlist.

Who can participate

Healthy volunteers accepted: No

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

Inclusion criteria

  • Male sex
  • Age between 25 - 50 years
  • German speaking
  • Current major depression (assessed by SCID-5)
  • Informed consent as documented by signature

Exclusion criteria

  • Inability to give informed consent
  • Prior hormonal (testosterone) treatment
  • Prior mental health disorder
  • Current or previous psychopharmacological treatment
  • Current or previous psychological treatment for any psychological disorder
  • Exception for persistent depressive disorder (Dysthymia) and alcohol/substance use disorder of mild degree (SCID-5, 1 - 3 criteria met)
  • Comorbidities of major depression with any other psychological disorder
  • Severe physical disorder that requires priority treatment
  • Any of the following physical conditions, particularly relevant in regard to testosterone treatment:
  • Diagnosed prostate cancer
  • Prostatic intraepithelial neoplasia (PIN)
  • Severe lower urinary tract symptoms
  • Erythrocytosis Sleep apnea, diagnosed but untreated
  • Current treatment with:
  • Thyroid hormones
  • Finasteride
  • Antiepileptic drugs
  • Anabolic compounds
  • Hypnotic medication more than 2 nights/week for the treatment of insomnia
  • Long-acting benzodiazepines
  • Antipsychotic medication
  • Drugs that affect serum testosterone
  • Genetic / hormonal disorders:
  • Klinefelter's syndrome
  • Cushing's disease
  • Addison's disease
  • Hashimoto Thyroiditis

Treatment and study plan

Male-specific psychotherapeutic program (MSPP)

Behavioral

The MSPP for MDD is designed to be used for the acute treatment of depression in men in 18 sessions over a period of 18 weeks. Therapy is delivered weekly with homework bridging every session. Central CBT elements (e.g. behavioral activation, cognitive restructuring) will be retained in MSPP. During implementation of typical CBT techniques, masculine role norms will be considered. One underlying topic will be the potential of multiple masculinities to coexist, being fluid and relational within one man, emphasizing positive aspects of masculinities compatible with psychotherapy for MDD.

Cognitive beahvioral therapy (CBT)

Behavioral

This intervention consists of 18 sessions of manualized, standard cognitive behavioral therapy for major depression. Therapy is delivered weekly with homework bridging every session.

Primary outcomes

  1. Change from baseline observer assessed depressive symptomatology to post treatment

    Time frame: baseline / 24 weeks

    Observer assessed depressive symptomatology measured with the Hamilton Depression Rating Scale (HDRS-21)

  2. Changes in the clinical symptomatology from baseline to post treatment

    Time frame: baseline / 24 weeks

    Observer assessed clinical symptomatology measured with the Clinical Global impression Scale (CGI-S/I)

  3. Change from baseline male typical depressive symptomatology to post treatment

    Time frame: baseline / 24 weeks

    Self-reported male typical depression symptoms including externalizing behavior such as aggression, risk taking, or alcohol consumption measured with the Male Depression Risk Scale (MDRS-22)

  4. Change from baseline self-reported depressive symptomatology to post treatment

    Time frame: baseline / 24 weeks

    self-reported depressive symptomatology measured with the Beck Depression Inventory (BDI-II)

  5. Changes in gender role conflict

    Time frame: baseline / 24 weeks

    Self-reported symptoms of gender role conflict measured with the Gender Role Conflict Scale (GRCS-16)

  6. Drop out

    Time frame: at follow up week 36

    Acceptability: Proportion of men who withdraw for any reason (dropout) will be recorded and if dropped out participants consent, a dropout interview will be conducted to examine the reasons for dropout.

  7. Achieved remission

    Time frame: post treatment week 24

    Proportion of participants, that achieved depressive symptom remission (assessed by structured clinical interview [SCID-5-CV] for DSM-V disorders)

  8. Changes in the therapeutic alliance quality

    Time frame: week 6 / week 24

    Self reported working alliance quality with the therapist

Secondary outcomes

  1. Skala Suizidales Erleben und Verhalten (SSEV-9)

    Time frame: baseline / week 6 / week 15 / post treatment week 24 / follow up week 36

    Self-reported suicidal experience and behavior

  2. Suicide Cognitions Scales (SCS-18)

    Time frame: baseline / week 6 / week 15 / post treatment week 24 / follow up week 36

    Self-reported attitudes toward suicide

  3. Problematic Pornography Consumption Scale (PPCS-18)

    Time frame: baseline / week 6 / week 15 / post treatment week 24 / follow up week 36

    Self-reported pornography use and problematic consumption

  4. Alcohol Use Disorder Test 10 (AUDIT-10)

    Time frame: baseline / week 6 / week 15 / post treatment week 24 / follow up week 36

    Self-reported alcohol consumption symptomatology

  5. International Index of Erectile Function 15 (IIEF-15)

    Time frame: baseline / week 6 / week 15 / post treatment week 24 / follow up week 36

    Self-reported sexual dysfunction and libido symptomatology

  6. Perceived Stress Scale (PSS-10)

    Time frame: baseline / week 6 / week 15 / post treatment week 24 / follow up week 36

    Self-reported subjective stress

  7. Generalized Anxiety Disorder (GAD-7)

    Time frame: baseline / week 6 / week 15 / post treatment week 24 / follow up week 36

    Self-reported general anxiety

  8. Conformity Masculine Norms Inventory (CMNI-30)

    Time frame: baseline / week 6 / week 15 / post treatment week 24 / follow up week 36

    Self-reported conformity to traditional male role norms

  9. Male Role Norms Inventory - Short Form (MRNI-SF-21)

    Time frame: baseline / week 6 / week 15 / post treatment week 24 / follow up week 36

    Self-reported socially learned male role norms

  10. Precarious Manhood Beliefs Scale (PMB-4)

    Time frame: baseline / week 6 / week 15 / post treatment week 24 / follow up week 36

    Self-reported precarious manhood beliefs

  11. Loneliness Scale (LS-20)

    Time frame: baseline / week 6 / week 15 / post treatment week 24 / follow up week 36

    Self-reported feeling of loneliness and social isolation

  12. Self-Compassion Scale D (SCS-D 10)

    Time frame: baseline / week 6 / week 15 / post treatment week 24 / follow up week 36

    Self-reported Positive attitude towards oneself in difficult life situations

  13. Emotion Regulation Questionnaire (ERQ-10)

    Time frame: baseline / week 6 / week 15 / post treatment week 24 / follow up week 36

    Self-reported tendency to re-evaluate / suppress emotions

  14. General Belongingness Scale (GBS)

    Time frame: baseline / week 6 / week 15 / post treatment week 24 / follow up week 36

    Self-reported achieved belongingness

  15. CIDI-Traumaliste (CIDI-T-12)

    Time frame: baseline / week 6 / post treatment week 24 / follow up week 36

    Assessment of self-reported traumatic experiences over the life span

  16. International Trauma Questionnaire (ITQ-18)

    Time frame: baseline / week 6 / post treatment week 24 / follow up week 36

    Self-reported core symptoms of post-traumatic stress disorder and complex post-traumatic stress disorder

  17. Agression Questionnaire Buss and Perry (AQ-BP)

    Time frame: baseline / week 6 / post treatment week 24 / follow up week 36

    Self-reported anger and aggression symptomatology

  18. Fragebogens zum Körperbild (FKB-6)

    Time frame: baseline / week 6 / post treatment week 24 / follow up week 36

    Self-reported attitudes towards one's own and an ideal body image

  19. Male Body Attitudes Scale-Revised (MBAS-R-15)

    Time frame: baseline / week 6 / post treatment week 24 / follow up week 36

    Self-reported male-specific body (dis)satisfaction

  20. Body Appreciation Scale 2 (BAS-2-10)

    Time frame: baseline / week 6 / post treatment week 24 / follow up week 36

    Self-reported assessment of a positive body image

  21. Stigma questionnaire (STIG-9)

    Time frame: baseline / week 6 / post treatment week 24 / follow up week 36

    Self-reported experienced stigma for suffering from a mental illness

  22. Self-stigma of seeking psychological help (SSOSH-10)

    Time frame: baseline / week 6 / post treatment week 24 / follow up week 36

    Self-reported experienced stigma of seeking help

  23. SHAME Questionnaire (SHAME-21)

    Time frame: baseline / week 6 / post treatment week 24 / follow up week 36

    Self-reported physical, cognitive and existential shame

  24. Test of Self-Conscious Affect (TOSCA-16)

    Time frame: baseline / week 6 / post treatment week 24 / follow up week 36

    Assessment of susceptibility to guilt, shame, externalization, and unconcern (self-report questionnaire).

  25. Toronto Alexithymia Scale (TAS-20)

    Time frame: baseline / week 6 / post treatment week 24 / follow up week 36

    Self-reported difficulty identifying and describing emotions

  26. Multidimensional Self-Concept Scale (MSCS)

    Time frame: baseline / week 6 / post treatment week 24 / follow up week 36

    Self-reported self-concept (self-worth)

  27. Arnett Inventory of Sensation Seeking (AISS-20)

    Time frame: baseline / week 6 / post treatment week 24 / follow up week 36

    Self-reported seeking of intense experiences including risky behavior

  28. Need to Belong Scale (NTBS-10)

    Time frame: baseline / week 6 / post treatment week 24 / follow up week 36

    Self-reported motivation to be accepted by others and avoidance of rejection by others

Other outcomes

  1. Body composition

    Time frame: baseline / week 6 / week 15 / post treatment week 24 / follow up week 36

    Body composition is determined by using bioelectrical impedance analysis (BIA)

  2. Blood testosteron

    Time frame: baseline / week 6 / week 15 / post treatment week 24 / follow up week 36

    Blood samples are collected at each study visit to assess blood testosterone

  3. Hair testosterone

    Time frame: baseline / week 6 / week 15 / post treatment week 24 / follow up week 36

    Hair samples are collected at each study visit to assess hair testosterone

  4. Grip strength

    Time frame: baseline / week 6 / week 15 / post treatment week 24 / follow up week 36

    Grip strength will be assessed with a basic hydraulic hand dynamometer at each study visit

Study contacts

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

Andreas Walther, PhD

CONTACT

[email protected]

+41 78 307 18 16

Ulrike Ehlert, Professor

CONTACT

[email protected]

+41 44 635 73 50

Sponsors and collaborators

Lead sponsor

Andreas Walther

Other

Registry information

Official study title

Evaluation of a Male-specific Psychotherapeutic Program for Major Depressive Disorders Compared to Standard Cognitive Behavioral Therapy: a Randomized Controlled Superiority Trial

Acronym: MSPP-MDD

Important dates

Study start
2023
Primary completion
2025
Study completion
2025
First posted
Jun 28, 2022
Registry last updated
Mar 28, 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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