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The effect of the computer- based training package on quality of life and symptom severity in andropausal men

The effect of the computer- based training package on quality of life and symptom severity in andropausal men

Status
Active, not recruiting
Phases
Phase 3
Study type
Interventional
Source
IRCT
Registry ID
IRCT201407166777N3
Enrollment
80
Registered
2014-11-03
Start date
2014-08-23
Completion date
Unknown
Last updated
2018-02-22

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

Conditions

andropause. -----

Interventions

Intervention 1: Intervention group: Computer-based training will be held for the men in the intervention group in the form of 4 sessions over a period of 4 weeks. Two months after the intervention, Q
Lifestyle
Intervention group: Computer-based training will be held for the men in the intervention group in the form of 4 sessions over a period of 4 weeks. Two months after the intervention, QoL and symptom s
Control group: Computer-based training won't be held for the men in the control group. In the control group will be asked to complete the questionnaires again, two months after the initial test. Fina

Sponsors

Vice Chancellor for research of Tehran University of Medical Sciences
Lead Sponsor

Eligibility

Sex/Gender
Male
Age
53 Years to 33 Years

Inclusion criteria

Inclusion criteria: Inclusion criteria: Proficiency in Persian, being emotionally and physically able to answer questions, being married, having at least high school education, having access to computers, being able to work with the computer to the extent that the training package be used, lack of chronic diseases & mental disorders, lack of disability. Exclusion criteria: Unwillingness to participate in the study, incomplete responses to the questionnaire, being affected with a chronic disease and mental disorder during the study.

Exclusion criteria

Exclusion criteria:

Design outcomes

Primary

MeasureTime frame
Quality Of Life. Timepoint: Before the experiment, two months after the intervention. Method of measurement: Questionnaire Sf36.;Symptoms Severity. Timepoint: Before the experiment, two months after the intervention. Method of measurement: AMS Questionnaire.

Secondary

MeasureTime frame
-----. Timepoint: ------. Method of measurement: ------.

Countries

Iran (Islamic Republic of)

Contacts

Public ContactElahe afsharnia

Tehran univesity of medical science

Elahe.afsharnia@yahoo.com+98 910 576 2775

Outcome results

None listed

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