Ireland
--:--IST
Recruiting Not applicable

Aerobic Exercise and Guided Imagery in Low Anterior Resection Syndrome

NCT07732894 · tracked via the Priya Life Science Turkey tracker
Phase
Not applicable
Started
2025-12-30
Last updated
2026-07-29

Condition(s) studied

Rectal CancerFecal Incontinence and ConstipationAerobic ExerciseGuided Imagery ExercisePelvic Floor Physical TherapyPelvic Floor Muscle Training

Investigational drug(s) / intervention(s)

Exerciseguided imagery

Exercise: structured walking exercise, at the clinic and outside from the clinic for at least 3 days /week

guided imagery: guided imagery for at least 3 days

Study summary

Low Anterior Resection Syndrome (LARS) is a common complication after sphincter-preserving rectal cancer surgery and may negatively affect bowel function and quality of life. Although exercise has been shown to improve physical function and well-being in cancer survivors, evidence regarding its effects on LARS symptoms remains limited.

This randomized controlled, multicenter study aims to evaluate the effects of an aerobic exercise program combined with guided imagery on bowel symptoms, quality of life, physical activity level, functional capacity, and psychological well-being in patients with LARS after rectal cancer surgery. Participants will be randomly assigned to either an intervention group receiving aerobic exercise and guided imagery in addition to standard care or a control group receiving standard care alone. Outcomes will be assessed at baseline and after the intervention period using validated clinical and patient-reported outcome measures.

The findings of this study may contribute to the development of evidence-based rehabilitation strategies for improving bowel function and quality of life in patients with LARS following rectal cancer surgery.

Eligibility

Sex
ALL
Min age
18 Years
Max age
65 Years
Healthy volunteers
No
Inclusion Criteria: * Upper-Middle-Lower Rectal Cancer * Having undergone surgery with TMJ * Having a protective ileostomy and a closed stoma * Being tumor-free according to laboratory reports (carcinoembryonic antigen), endoscopic findings, and abdominal ultrasonography and/or computed tomography data * Having at least minor LARS scores ("between 21" and "42") according to the -LARS scoring questionnaire * Having the ability to perform voluntary perineal traction contractions with perineal palpation * Being a volunteer with informed consent Exclusion Criteria: * History of incontinence or defecation disorder not related to rectal cancer * Having another type of surgery for rectal cancer (Hartmann procedure, abdominoperineal excision, transanal endoscopic microsurgical resection, or sigmoid resection) * Deterioration in general health, neurological disease and/or physical disability * BMI \> 30 kg/m2 (obese individuals) * Inability to answer questions or make interventions due to mental disorder

Primary outcome measure(s)

  • Low Anterior Resection Sydrome scoring system — "From enrollment to the end of treatment at 8 weeks"
    It measures the intensity of low anterior resection syndrome. The score varies between "0" and "42". Higher scores indicates more severe symptoms.
  • European Organisation for Research and Treatment of Cancer Core Quality of Life Questionnaire-30 — 8 weeks from beginning the study
    It measures the quality of life in cancer patients. The scores range from 0 to 100. For the Global Health Status and Functional Scales, higher scores indicate better health-related quality of life and functioning, whereas for the Symptom Scales, higher scores indicate greater symptom burden.
  • European Organisation for Research and Treatment of Cancer Core Quality of Life Questionnaire-29 — 8 weeks
    It measures the quality of life in cancer patients. The EORTC QLQ-CR29 scores range from 0 to 100. Higher scores on the functional scales indicate better functioning, whereas higher scores on the symptom scales indicate greater symptom burden.
  • 6 minutes walking test — 8 weeks
    It measures the aerobic capacity within 6 minutes. The 6-Minute Walk Test (6MWT) assesses functional exercise capacity by measuring the total distance walked in meters over six minutes. There is no maximum value. Higher distances indicate better functional exercise capacity.

Trial sites (1)

FacilityCityRegionStatus
Memorial Bahçelievler Hospital Istanbul Turkey (Türkiye) Recruiting
Official registry record

This page summarises publicly available registry data for informational purposes — not medical advice. Eligibility is determined by each study team; patients should discuss participation with their clinician.

View NCT07732894 on ClinicalTrials.gov ↗ ← All trials in Turkey