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The effect of group counseling based on Pender model on quality of life in women with stress urinary incontinence

The effect of group counseling based on Pender's health promotion model on quality of life in women with stress urinary incontinence

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
IRCT
Registry ID
IRCT20211216053423N1
Enrollment
70
Registered
2022-03-14
Start date
2022-04-09
Completion date
Unknown
Last updated
2022-04-04

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

Conditions

Stress urinary incontinence. Stress incontinence (female) (male)

Interventions

Intervention 1: Intervention group: After obtaining written consent from the selected individuals and completing the sample selection form and confirming the absence of urinary tract infection after a

Sponsors

Mashhad University of Medical Sciences
Lead Sponsor

Eligibility

Sex/Gender
Female
Age
18 Years to No maximum

Inclusion criteria

Inclusion criteria: Have informed consent to participate in research. Be Iranian. Be over 18 years old. Be at least literate. Have a smartphone to call and follow up to participate in the study. not pregnant. Do not have any known disease related to urinary incontinence. Do not use drugs and diuretics. Do not use tobacco, drugs and alcohol. has no movement restrictions. Be able to communicate verbally. Have BMI less than 30. Do not have urinary tract infection. Having stress urinary incontinence based on getting a score of 4 and above from the first three questions of the QUID questionnaire. Do not have severe stress and anxiety (according to the DASS 21 Stress, Anxiety and Depression Questionnaire)

Exclusion criteria

Exclusion criteria: Not participating in counseling sessions for more than one session and not wanting to continue the intervention. Reluctance to continue cooperation in research. Have an unfortunate accident during the research.

Design outcomes

Primary

MeasureTime frame
Quality of Life. Timepoint: Before the intervention, immediately after the intervention, 2 months after the intervention. Method of measurement: Standard Questionnaire for Quality of Life in People with Urinary Incontinence.

Countries

Iran (Islamic Republic of)

Contacts

Public ContactMahtab Mahvashi

Mashhad University of Medical Sciences

mahvashim982@mums.ac.ir+98 51 3859 1511

Outcome results

None listed

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