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Mobile Phone Applications Education In SCI

The effect of mobile-based APP education on sexual adjustment sexual satisfaction, marital adjustment and marital satisfaction of men with spinal cord injury

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
IRCT
Registry ID
IRCT20181205041861N2
Enrollment
70
Registered
2019-07-08
Start date
2019-07-10
Completion date
Unknown
Last updated
2020-02-24

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

Conditions

Sexual adjusment. Counselling related to sexual attitude

Interventions

Intervention 1: Intervention group: The application is designed to be installed on the smartphone of the intervention group eg
Men with spinal cord injury and its use is explained. The intervention consists of three phases of pre-test, content training, and post-test. The app is designed to allow active training content to be

Sponsors

Tehran University of Medical Sciences
Lead Sponsor

Eligibility

Sex/Gender
Male
Age
18 Years to No maximum

Inclusion criteria

Inclusion criteria: The mere man's involvement in spinal cord injury Type of incomplete or complete traumatic spinal cord injury Duration of damage for one year or more Having aged over 18 years old Ability to speak Persian,Interested in participating in the study At least one year of life in common marriage Not attending couples' training classes before the study Having a minimum level of literacy Having a mobile phone with Android system The age difference of couples is less than or equal to 10 years Not having a history of infertility

Exclusion criteria

Exclusion criteria: People whose spinal cord injury is due to other diseases or non-traumatic causes. History of or chronic psychological disorders such as depression and anxiety History of physical problems other than spinal cord injury Excessive brain damage leading to cognitive problems History of drug abuse and history of using psychiatric drugs in the last six months

Design outcomes

Primary

MeasureTime frame
Sexual adjustment. Timepoint: Before the intervention, 4 and 8 weeks after the intervention. Method of measurement: Hospital Anxiety and Depression Scale(SAQ).;Sexual Satisfaction. Timepoint: Before the intervention, 4 and 8 weeks after the intervention. Method of measurement: Sexual adjustment questionnaire Larson’s.;Marital adjustment. Timepoint: Before the intervention, 4 and 8 weeks after the intervention. Method of measurement: Spinner’s Marital adjustment.;Sexual-Satisfaction. Timepoint: Before the intervention, 4 and 8 weeks after the intervention. Method of measurement: Sexual-Satisfaction scale.

Secondary

MeasureTime frame
Mean score of Sexual Adjustment. Timepoint: Before the intervention, 4 and 8 weeks after the intervention. Method of measurement: Via Hospital Anxiety and Depression Scale (SAQ).;Mean score of Sexual satisfaction. Timepoint: Before the intervention, 4 and 8 weeks after the intervention. Method of measurement: Larson’s Sexual-Satisfaction scale.;Mean score of Marital adjustment. Timepoint: Before the intervention, 4 and 8 weeks after the intervention. Method of measurement: Spinner’s’ Marital adjustment questionnaire.;Mean score of Marital satisfaction. Timepoint: Before the intervention, 4 and 8 weeks after the intervention. Method of measurement: Via Marital Satisfaction ENRICH.

Countries

Iran (Islamic Republic of)

Contacts

Public ContactFatemeh Zarei

Tarbiat Modares University

f.zarei@modares.ac.ir+98 21 8288 4546

Outcome results

None listed

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