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Mind-body intervention practice (MBIP)as a complementary and integrative treatment (CIT)for compulsive sexual behavior disorder (CSBD): randomized controlled trial (RCT)

Mind-body intervention practice (MBIP)as a complementary and integrative treatment (CIT)for compulsive sexual behavior disorder (CSBD): randomized controlled trial (RCT)

Status
Recruiting
Phases
Unknown
Study type
Interventional
Source
REBEC
Registry ID
RBR-26k7hr
Enrollment
Unknown
Registered
2020-07-31
Start date
2021-03-15
Completion date
Unknown
Last updated
2025-10-27

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

V - Mental and behavioral disorders

Interventions

Mind-body intervention protocol practice (n = 30) and sham intervention protocol practice (n = 30), during 12 weeks of daily executions, distributed in 12 weekly collective classes by videoconference
E02.760.169.063.500.387.750

Sponsors

hospital das clínicas da faculdade de medicina da univesidade de são Paulo
Lead Sponsor
hospital das clínicas da faculdade de medicina da univesidade de são Paulo
Collaborator

Eligibility

Sex/Gender
Male
Age
18 Years to 90 Years

Inclusion criteria

Inclusion criteria: Brazilians; aged 18 or over; literate; with a satisfactory cognitive level to understand and answer the self-responsive inventories; available to participate in a 12-week intervention program; have a minimum score of 28 on the Sexual Compulsiveness Scale or have a minimum score of 20 on the Hypersexual Disorder Screening Inventory; present a minimum score of 14 in the Beck Anxiety Inventory.

Exclusion criteria

Exclusion criteria: Individuals who meet DSM-5 diagnostic criteria for Substance-Related Disorder and Addictive Disorders; Paraphilic Disorders; Gender dysphoria; Spectrum of Schizophrenia and other Psychotic Disorders; Hypomanic or Manic episode of Mood Disorder; Neurocognitive Disorders and other Mental Disorders; individuals who have already have practiced kundalini yoga; individuals who use psychiatric medication and cannot maintain the stability and regularity of the dosage three months before and during the intervention program; individuals who have attended psychotherapy in the last six months in weekly sessions and with at least 75% attendance; Individuals who have significant spinal problems and / or physical limitations that may interfere with intervention mind-body practice, for example, overweight, severe lung and / or cardiovascular disease.

Design outcomes

Primary

MeasureTime frame
Expected outcome 1 any decrease in the score of symptoms on the sexual compulsion scale, measured using data collected before the interventions and after the interventions, in the fourth week, in the eighth week and in the twelfth week

Secondary

MeasureTime frame
Expected outcome 3 any reduction in the severity of anxiety in the Beck anxiety inventory score, measured using data collected before the interventions and after the interventions, in the fourth week, in the eighth week and in the twelfth week;Expected outcome 1 any reduction in the severity of impulsivity in the impulsivity barrat score, measured using data collected before the interventions and after the interventions, in the fourth week, in the eighth week and in the twelfth week;Expected outcome 2 any reduction in the severity of hypersexuality in the score of the hypersexual disorder screening inventory, measured using data collected before the interventions and after the interventions, in the fourth week, in the eighth week and in the twelfth week;Expected outcome 4 any reduction in the severity of depression in the Beck depression inventory score, measured using data collected before the interventions and after the interventions, in the fourth week, in the eighth week and in the twelfth week;Expected outcome 5 any improvement in the level of quality of life in the WHO quality of life scale score, using data collected before the interventions and after the interventions, in the twelfth week;Expected outcome 6 any improvement in the regulation of sexual inhibition in the sexual inhibition scale score, using data collected before the interventions and after the interventions, in the twelfth week;Expected outcome 7 any improvement in the regulation of sexual arousal in the sexual arousal scale score, using data collected before the interventions and after the interventions, in the twelfth week;Expected outcome 8 any decrease in the severity of sexual dysfunction in the score of the international index of erectile function, through data collected before the interventions and after the interventions, in the twelfth week;Expected outcome 9 satisfactory adherence to treatment with a frequency of 70% of the 12 video classes and 70% of the daily executions of the mind-

Countries

Brazil

Contacts

Public ContactMarco Scanavino

hospital das clínicas da faculdade de medicina da univesidade de são Paulo

scanavino@gmail.com55 11 2661 6984

Outcome results

None listed

Source: REBEC (via WHO ICTRP)