The effect of using the application on the quality of life of women with pelvic organ prolapse

Investigating the effect of self-care application compared to routine care on the quality of life of patients with pelvic organ prolapse.

Status

Recruiting

Phases

Unknown

Study type

Interventional

Source

IRCT

Registry ID

IRCT20230923059497N1

Enrollment

Registered

2023-12-02

Start date

2023-11-27

Completion date

Unknown

Last updated

2024-01-22

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

Conditions

pelvic organ prolapse.. Perineocele

Interventions

Intervention 1: "Intervention group:" These people watch and practice pelvic floor muscle strengthening exercises with the application 30 minutes a day for 2 months and have access to the educational

Eligibility

Sex/Gender

Female

Inclusion criteria

Inclusion criteria: Having symptoms of pelvic organ prolapse Physician confirmation by examination for prolapse less or equal to III according to POP-Q Having a smartphone or tablet under the Android system The ability to use a smartphone Literate to read and write

Exclusion criteria

Exclusion criteria: Suffering from any type of urinary incontinence with a moderate to high degree based on the ICIQ-UI SF questionnaire Use of neuroleptics Use of antagonists pregnancy Celibacy History of pelvic physiotherapy in the last year History of pelvic surgery in the last year Childbirth in the past year Use of pessary

Design outcomes

Primary

Measure	Time frame
The score obtained in the quality of life questionnaire for prolapse disorders. Timepoint: The beginning of the study (before the start of the intervention) and two months after its start. Method of measurement: Quality of life questionnaire for prolapse disorders.;Degree of prolapse. Timepoint: The beginning of the study (before the start of the intervention) and two months after its start. Method of measurement: POP-Q system.	—

Measure

Time frame

The score obtained in the quality of life questionnaire for prolapse disorders. Timepoint: The beginning of the study (before the start of the intervention) and two months after its start. Method of measurement: Quality of life questionnaire for prolapse disorders.;Degree of prolapse. Timepoint: The beginning of the study (before the start of the intervention) and two months after its start. Method of measurement: POP-Q system.

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Secondary

Measure	Time frame
The score obtained in the prolapse knowledge questionnaire. Timepoint: At the beginning of the study (before the start of the intervention) and two months after the intervention. Method of measurement: Prolapse knowledge questionnaire.;The score obtained in the incontinence questionnaire. Timepoint: At the beginning of the study (before the start of the intervention) and two months after the intervention. Method of measurement: Incontinence knowledge questionnaire.	—

Measure

Time frame

The score obtained in the prolapse knowledge questionnaire. Timepoint: At the beginning of the study (before the start of the intervention) and two months after the intervention. Method of measurement: Prolapse knowledge questionnaire.;The score obtained in the incontinence questionnaire. Timepoint: At the beginning of the study (before the start of the intervention) and two months after the intervention. Method of measurement: Incontinence knowledge questionnaire.

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Countries

Iran (Islamic Republic of)

Contacts

Public ContactZahra Hadizadeh talasaz

Mashhad University of Medical Sciences

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

Outcome results

None listed

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