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The effectiveness of PLISSIT, a sexual counseling model on sexual function and sexual adaption of women with spinal codr injury

The effectiveness of PLISSIT, a sexual counseling model on sexual function and sexual adaption of women with spinal codr injury refered to Brain and spinal injury Repair Research Center(BASIR), Institution of Neouroscience

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
IRCT
Registry ID
IRCT2017061631662N3
Enrollment
50
Registered
2017-07-30
Start date
2017-07-06
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

Spinal cord injury. Cerebral palsy and other paralytic syndromes

Interventions

The control group will receive routine care (an educational pamphlet ).
Intervention 1: Intervention group will receive three 45 minute PLISSIT based (the first three stages) individual sexual counseling sessions weekly. Stage1: Permission Stage 2: Limited information S
Behavior
Intervention group will receive three 45 minute PLISSIT based (the first three stages) individual sexual counseling sessions weekly. Stage1: Permission Stage 2: Limited information Stage3: Specif

Sponsors

Alborz University of Medical Sciences
Lead Sponsor

Eligibility

Sex/Gender
Female
Age
18 Years to 50 Years

Inclusion criteria

Inclusion criteria: Inclusion criteria: participating in sessions regularly; having sexual activity; incomplete spinal cord injury; ability to read and write; to be available in the future month; having Iranian nationality; not having sexual disorder and chronic disease in partner. Exclusion criteria: become pregnant; marriage conflicts; occurring bitter events (death,...); well-known disease influence on sexual function; use some drugs that influence on sexual function.

Exclusion criteria

Exclusion criteria:

Design outcomes

Primary

MeasureTime frame
Sexual function. Timepoint: Before, 4 weeks , and 8 weeks after intervention. Method of measurement: FSFI questionnaire.;Sexual adaptation. Timepoint: Before, 4 weeks , and 8 weeks after intervention. Method of measurement: SAQ.

Countries

Iran (Islamic Republic of)

Contacts

Public ContactRazieh Lotfi

Alborz University of Medical Sciences- School of Nursing and Midwifery

raziehlotfi@abzums.ac.ir+98 26 3430 4433

Outcome results

None listed

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