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OncoMatch/Clinical Trials/NCT07732894

Aerobic Exercise and Guided Imagery in Low Anterior Resection Syndrome

Is NCT07732894 recruiting? Yes, currently enrolling (Sep 2026). This NA trial studies non-drug interventions for rectal cancer.

NARecruitingBiruni UniversityNCT07732894Data as of Sep 2026Location: Turkey (Türkiye)

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.

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Extracted eligibility criteria

Cancer type

Colorectal Cancer

Demographics

Ages ≤ 65

Prior therapy

Must have received: surgery with TMJ

Having undergone surgery with TMJ

Cannot have received: Hartmann procedure

Having another type of surgery for rectal cancer (Hartmann procedure, abdominoperineal excision, transanal endoscopic microsurgical resection, or sigmoid resection)

Cannot have received: abdominoperineal excision

Having another type of surgery for rectal cancer (Hartmann procedure, abdominoperineal excision, transanal endoscopic microsurgical resection, or sigmoid resection)

Cannot have received: transanal endoscopic microsurgical resection

Having another type of surgery for rectal cancer (Hartmann procedure, abdominoperineal excision, transanal endoscopic microsurgical resection, or sigmoid resection)

Cannot have received: sigmoid resection

Having another type of surgery for rectal cancer (Hartmann procedure, abdominoperineal excision, transanal endoscopic microsurgical resection, or sigmoid resection)

Structured fields extracted by AI. May contain errors — verify against the official protocol.

Frequently asked questions

Is NCT07732894 currently recruiting?

Yes, this trial is currently recruiting patients.

Are there prior therapy exclusions?

Yes. Prior Hartmann procedure, abdominoperineal excision, transanal endoscopic microsurgical resection disqualifies patients from enrollment.

Is there an age limit?

Yes. Patients must be 65 years or younger.

Could you qualify for this trial?

Enter your biomarker results to see how this trial's eligibility criteria match your specific cancer profile.

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