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????? Influence of two regular physical activity interventions on sexual dysfunction and steroid level in female patients with major depressive disorders and undergoing a treatment with SSRIs

????? Influence of two regular physical activity interventions on sexual dysfunction and steroid level in female patients with major depressive disorders and undergoing a treatment with SSRIs – randomized interventional study

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
IRCT
Registry ID
IRCT20090304001743N16
Enrollment
45
Registered
2020-05-29
Start date
2020-09-22
Completion date
Unknown
Last updated
2020-06-15

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

Conditions

medication induced sexual dysfunction. Sedative, hypnotic or anxiolytic use, unspecified with sedative, hypnotic or anxiolytic-induced sexual dysfunction

Interventions

Intervention 1: Intervention group: endurance training,30-45 min in duration,for 12 consecutive weeks and consists of three weekly. After 5 min of warming-up and stretching, participants exercised for

Sponsors

Hamedan University of Medical Sciences
Lead Sponsor

Eligibility

Sex/Gender
Female
Age
18 Years to 50 Years

Inclusion criteria

Inclusion criteria: Major depressive disorders characterized by trained psychiatrists and clinical psychologists based on DSM-5 criteria SSRI-induced sexual dysfunction, diagnosed by an accurate clinical interview based on DSM-5 criteria Signing a written consent 18-50 years old

Exclusion criteria

Exclusion criteria: Pregnancy or intention to conceive during the study period or breastfeeding other psychiatric disorders

Design outcomes

Primary

MeasureTime frame
Sexual dysfunction. Timepoint: Before the intervention,3,6,9,12 weeks after the intervention. Method of measurement: Female Sexual Function Index score.;Steroid level in blood. Timepoint: Before the intervention,12 weeks after the intervention. Method of measurement: level of Estrogen,Progesterone, testosterone,Cortisol in Blood.

Secondary

MeasureTime frame
Emotion Regulation. Timepoint: Before the intervention, 6,12 weeks after the intervention. Method of measurement: emotional competencies inventory.;Social activity. Timepoint: Before the intervention, 6,12 weeks after the intervention. Method of measurement: Social Adaptation Self-evaluation Scale.;Depressive symptoms. Timepoint: Before the intervention,3, 6,9,12 weeks after the intervention. Method of measurement: Beck Depression Inventory-Fast Screen.;Hypomania. Timepoint: Before the intervention, 6,12 weeks after the intervention. Method of measurement: Hypomania Check List 32.;Insomnia. Timepoint: Before the intervention,3, 6,9,12 weeks after the intervention. Method of measurement: Insomnia Severity Index.;Physical activity. Timepoint: Before the intervention, 6,12 weeks after the intervention. Method of measurement: International Physical Activity Questionnaire (IPAQ).

Countries

Iran (Islamic Republic of)

Contacts

Public ContactMohammad Haghighi

Hamedan University of Medical Sciences

haghighi@umsha.ac.ir+98 81 3827 1066

Outcome results

None listed

Source: IRCT (via WHO ICTRP) · Data processed: Feb 4, 2026