Ambulatory for Cognitive Behavioral Therapy and Behavioral Medicine of the University of Zurich
Zurich, Canton of Zurich, 8032, Switzerland
Location status: Recruiting
Location contact
Simona Palm, PhD
CONTACT
Ulrike Ehlert, Professor
CONTACT
NCT Number: NCT05435222
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.
Interested in participating?
Request Info25 year–50 year
Male
Interventional
Not applicable
Zurich, Canton of Zurich, 8032, Switzerland
Location status: Recruiting
Simona Palm, PhD
CONTACT
Ulrike Ehlert, Professor
CONTACT
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.
Healthy volunteers accepted: No
Only the study team can determine whether someone qualifies for participation.
Inclusion criteria
Exclusion criteria
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.
This intervention consists of 18 sessions of manualized, standard cognitive behavioral therapy for major depression. Therapy is delivered weekly with homework bridging every session.
Time frame: baseline / 24 weeks
Observer assessed depressive symptomatology measured with the Hamilton Depression Rating Scale (HDRS-21)
Time frame: baseline / 24 weeks
Observer assessed clinical symptomatology measured with the Clinical Global impression Scale (CGI-S/I)
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)
Time frame: baseline / 24 weeks
self-reported depressive symptomatology measured with the Beck Depression Inventory (BDI-II)
Time frame: baseline / 24 weeks
Self-reported symptoms of gender role conflict measured with the Gender Role Conflict Scale (GRCS-16)
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.
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)
Time frame: week 6 / week 24
Self reported working alliance quality with the therapist
Time frame: baseline / week 6 / week 15 / post treatment week 24 / follow up week 36
Self-reported suicidal experience and behavior
Time frame: baseline / week 6 / week 15 / post treatment week 24 / follow up week 36
Self-reported attitudes toward suicide
Time frame: baseline / week 6 / week 15 / post treatment week 24 / follow up week 36
Self-reported pornography use and problematic consumption
Time frame: baseline / week 6 / week 15 / post treatment week 24 / follow up week 36
Self-reported alcohol consumption symptomatology
Time frame: baseline / week 6 / week 15 / post treatment week 24 / follow up week 36
Self-reported sexual dysfunction and libido symptomatology
Time frame: baseline / week 6 / week 15 / post treatment week 24 / follow up week 36
Self-reported subjective stress
Time frame: baseline / week 6 / week 15 / post treatment week 24 / follow up week 36
Self-reported general anxiety
Time frame: baseline / week 6 / week 15 / post treatment week 24 / follow up week 36
Self-reported conformity to traditional male role norms
Time frame: baseline / week 6 / week 15 / post treatment week 24 / follow up week 36
Self-reported socially learned male role norms
Time frame: baseline / week 6 / week 15 / post treatment week 24 / follow up week 36
Self-reported precarious manhood beliefs
Time frame: baseline / week 6 / week 15 / post treatment week 24 / follow up week 36
Self-reported feeling of loneliness and social isolation
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
Time frame: baseline / week 6 / week 15 / post treatment week 24 / follow up week 36
Self-reported tendency to re-evaluate / suppress emotions
Time frame: baseline / week 6 / week 15 / post treatment week 24 / follow up week 36
Self-reported achieved belongingness
Time frame: baseline / week 6 / post treatment week 24 / follow up week 36
Assessment of self-reported traumatic experiences over the life span
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
Time frame: baseline / week 6 / post treatment week 24 / follow up week 36
Self-reported anger and aggression symptomatology
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
Time frame: baseline / week 6 / post treatment week 24 / follow up week 36
Self-reported male-specific body (dis)satisfaction
Time frame: baseline / week 6 / post treatment week 24 / follow up week 36
Self-reported assessment of a positive body image
Time frame: baseline / week 6 / post treatment week 24 / follow up week 36
Self-reported experienced stigma for suffering from a mental illness
Time frame: baseline / week 6 / post treatment week 24 / follow up week 36
Self-reported experienced stigma of seeking help
Time frame: baseline / week 6 / post treatment week 24 / follow up week 36
Self-reported physical, cognitive and existential shame
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).
Time frame: baseline / week 6 / post treatment week 24 / follow up week 36
Self-reported difficulty identifying and describing emotions
Time frame: baseline / week 6 / post treatment week 24 / follow up week 36
Self-reported self-concept (self-worth)
Time frame: baseline / week 6 / post treatment week 24 / follow up week 36
Self-reported seeking of intense experiences including risky behavior
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
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)
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
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
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
Contact information is provided by the study sponsor or research team.
Andreas Walther, PhD
CONTACT
Ulrike Ehlert, Professor
CONTACT
Andreas Walther
Other
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
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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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