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Recruiting NCT06628674

Developing and Testing the Effect of Online Interactive Videos in Improving Low Anterior Resection Syndrome.

No phase Interventional Rectal Cancer

For patients and families

In plain language

An automatic summary of structured registry data. It is an orientation aid, not a substitute for the official protocol or a physician assessment.

What is being studied
The protocol lists: core muscle exercise, pelvic muscle exercise.
Who it may be relevant to
Registry conditions: Rectal Cancer. Basic parameters: from 20 years · All.
What needs checking
Age, condition and sex are only basic indicators. Prior treatment, laboratory values and other mandatory requirements appear in the eligibility criteria below.
Where it takes place
Taiwan
Next step
Save the trial, show it to the treating physician, and confirm current recruitment with the study center. Costs, documents and travel →

Unsure about the terms? Read our patient guide →

Official title

Developing and Testing the Effect of Online Interactive Videos in Improving Low Anterior Resection Syndrome, Psychological Distress,and Quality of Life

Overview

This study aims to develop and test the effect of online interactive videos in improving LARS.

Interventions

  • Behavioral core muscle exercise
    Patients in experiment group will do core muscle exercise with online interactive videos
  • Behavioral pelvic muscle exercise
    Patients in experiment group will do pelvic muscle exercise without online interactive videos

Primary outcome measures

  • Self-report Questionnaire [Time frame: Change from baseline symptom to 6 months after intervention]

Eligibility criteria

Inclusion criteria

  • Stage I-III rectal cancer.
  • Patients already know their condition.
  • Aged 20 years and older.
  • Consciously communicate in Mandarin or Taiwanese.
  • Agreed with the interview and had signed the permit.

Exclusion criteria

  • Recurrent rectal cancer.
  • Stage IV rectal cancer.

Criteria are shown verbatim from the registry (in English). Final eligibility is always assessed by the study center.

Healthy volunteers: No

Study design

Allocation
Randomized
Model
Parallel assignment
Masking
Single blind
Primary purpose
Supportive care

Study locations

Taiwan · 1 center
  • Chang Gung Memorial Hospital, Linkou — Taoyuan

Identifiers

NCT: NCT06628674 · 202301931B0

Primary sources (government registries)

View this study on ClinicalTrials.gov ↗