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Study on the effect of DSP4Health digital health service package combined with pelvic floor rehabilitation therapy instrument on women with pelvic floor dysfunction in community

Study on the effect of DSP4Health digital health service package combined with pelvic floor rehabilitation therapy instrument on women with pelvic floor dysfunction in community

Status
Active, not recruiting
Phases
Unknown
Study type
Observational
Source
ChiCTR
Registry ID
ChiCTR2400088675
Enrollment
Unknown
Registered
2024-08-23
Start date
2024-10-01
Completion date
Unknown
Last updated
2024-08-26

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

Conditions

pelvic floor dysfunction

Interventions

Intervention group (After the completion of a pelvic floor rehabilitation device treatment, the study subjects were given the installation and use of digital health service package to ensure that the
Control group (Routine pelvic floor rehabilitation in outpatient department):None

Sponsors

Shanghai Changning District Center for Disease Control and Prevention
Lead Sponsor

Eligibility

Sex/Gender
Female
Age
50 Years to 75 Years

Inclusion criteria

Inclusion criteria: (1) Between the ages of 50 and 75, with a history of childbearing; (2) The duration of the disease ranged from 6 months to 10 years; (3) Those who meet the clinical diagnostic criteria for stress incontinence and have mild to moderate severity according to the Ingelman-Sundberg scale; (4) Those who met the clinical diagnostic criteria for pelvic organ prolapse, and the prolapse degree was stage I and stage II according to POP-Q score method; (5) Have normal communication and understanding ability; (6) No vision, hearing impairment, no history of mental illness; (7) Volunteer to participate in this study, sign informed consent, and agree to participate in follow-up visits and questionnaires.

Exclusion criteria

Exclusion criteria: (1) Patients with urethral dysfunction caused by lower urinary tract infection, diabetes, vesico-vaginal fistula, bladder tumor and trauma; (2) A history of pelvic floor surgery in the past six months; (3) suffers from chronic wasting disease or is in an acute episode of psychosis; (4) suffering from central nervous system disease or serious cardiopulmonary disease; (5) Vaginal bleeding; (6) Severe pelvic floor pain.

Design outcomes

Primary

MeasureTime frame
Improvement of pelvic floor dysfunction;ompliance;Health knowledge awareness;Self-perceived severity of symptoms;Quality of life;

Secondary

MeasureTime frame
Feasibility of digital packages;Acceptability of digital packages;Ease of use of digital packages;

Countries

China

Contacts

Public ContactJiabei He

Shanghai Changning District Center for Disease Control and Prevention

843641501@qq.com+86 133 2180 5927

Outcome results

None listed

Source: ChiCTR (via WHO ICTRP) · Data processed: Jun 25, 2026