A randomized controlled trial for the influence of Kegel exercise combined with electronic biofeedback therapy for low anterior resection syndrome in rectal cancer

Status

Active, not recruiting

Phases

Early Phase 1

Study type

Interventional

Source

ChiCTR

Registry ID

ChiCTR1900026345

Enrollment

Unknown

Registered

2019-10-01

Start date

2019-10-01

Completion date

Unknown

Last updated

2020-01-20

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

Conditions

Colorectal cancer

Interventions

group A:Kegel exercise joint electronic biofeedback therapy

group B:Kegel exercise

group C:Electronic biofeedback therapy

control group:blank control

Eligibility

Sex/Gender

All

Inclusion criteria

Inclusion criteria: 1. pathological diagnosis is a rectal malignancy; 2. aged 18 to 80 years; 3. have low anterior resction; 4. with preventive stoma; 5. informed constent of patients and their families and they are voluntary to join the study;

Exclusion criteria

Exclusion criteria: 1. Have a history of pelvic floor surgery; 2. women in pregnancy or lactation; 3. patients in acute inflammation such as colitis and Crohn's disease; 4. patients who cannot reverse the temporary stoma; 5. contraindications to biofeedback treatment.

Design outcomes

Primary

Measure	Time frame
Rectal anal pressure;low anterior resection syndrome score;	—

Secondary

Measure	Time frame
Quality of life score;	—

Countries

China

Contacts

Public ContactWang Xiaodong

The West China College of Medicine, Sichuan University

lockwan@qq.com+86 13882267388

Outcome results

None listed

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