NCT06628674

Brief Summary

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

Trial Health

77
On Track

Trial Health Score

Automated assessment based on enrollment pace, timeline, and geographic reach

Enrollment
110

participants targeted

Target at P50-P75 for not_applicable

Timeline
21mo left

Started Nov 2024

Typical duration for not_applicable

Geographic Reach
1 country

1 active site

Status
recruiting

Health score is calculated from publicly available data and should be used for screening purposes only.

Trial Relationships

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Study Timeline

Key milestones and dates

Study Progress47%
Nov 2024Jan 2028

First Submitted

Initial submission to the registry

October 4, 2024

Completed
4 days until next milestone

First Posted

Study publicly available on registry

October 8, 2024

Completed
1 month until next milestone

Study Start

First participant enrolled

November 15, 2024

Completed
2.7 years until next milestone

Primary Completion

Last participant's last visit for primary outcome

July 31, 2027

Expected
6 months until next milestone

Study Completion

Last participant's last visit for all outcomes

January 31, 2028

Last Updated

March 20, 2026

Status Verified

March 1, 2026

Enrollment Period

2.7 years

First QC Date

October 4, 2024

Last Update Submit

March 18, 2026

Conditions

Outcome Measures

Primary Outcomes (1)

  • Self-report Questionnaire

    Show the specific trajectory of LAR Syndrome, psychological distress and fecal incontinence-related QoL in patients with rectal cancer

    Change from baseline symptom to 6 months after intervention

Study Arms (2)

Core muscle exercise

EXPERIMENTAL
Behavioral: core muscle exercise

pelvic muscle exercise

OTHER
Behavioral: pelvic muscle exercise

Interventions

Patients in experiment group will do core muscle exercise with online interactive videos

Core muscle exercise

Patients in experiment group will do pelvic muscle exercise without online interactive videos

pelvic muscle exercise

Eligibility Criteria

Age20 Years+
Sexall
Healthy VolunteersNo
Age GroupsAdult (18-64), Older Adult (65+)

You may qualify if:

  • 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.

You may not qualify if:

  • Recurrent rectal cancer.
  • Stage IV rectal cancer.

Contact the study team to confirm eligibility.

Sponsors & Collaborators

Study Sites (1)

Chang Gung Memorial Hospital, Linkou

Taoyuan District, 中和區, 333, Taiwan

RECRUITING

MeSH Terms

Conditions

Rectal Neoplasms

Condition Hierarchy (Ancestors)

Colorectal NeoplasmsIntestinal NeoplasmsGastrointestinal NeoplasmsDigestive System NeoplasmsNeoplasms by SiteNeoplasmsDigestive System DiseasesGastrointestinal DiseasesIntestinal DiseasesRectal Diseases

Central Study Contacts

Yun-Jen Chou, PhD

CONTACT

Study Design

Study Type
interventional
Phase
not applicable
Allocation
RANDOMIZED
Masking
SINGLE
Who Masked
PARTICIPANT
Purpose
SUPPORTIVE CARE
Intervention Model
PARALLEL
Sponsor Type
OTHER
Responsible Party
SPONSOR

Study Record Dates

First Submitted

October 4, 2024

First Posted

October 8, 2024

Study Start

November 15, 2024

Primary Completion (Estimated)

July 31, 2027

Study Completion (Estimated)

January 31, 2028

Last Updated

March 20, 2026

Record last verified: 2026-03

Locations