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Published on: January 10, 2013
Triple-target treatment versus low-frequency electrostimulation for anal incontinence: a randomized, controlled trial
Thilo Schwandner1, Claudia Hemmelmann, Tankred Heimerl
1Klinik für Allgemein-, Viszeral-, Thorax- und Transplantationschirurgie, Fachbereich Medizin, Justus-Liebig-Universität Giessen.
Triple-target treatment (3T), combining amplitude-modulated medium-frequency stimulation and electromyographic biofeedback, significantly improved anal incontinence outcomes compared to low-frequency stimulation (LFS). 3T is recommended for clinical practice.
Area of Science:
- Coloproctology
- Pelvic floor rehabilitation
Background:
- Nonsurgical treatment for anal incontinence often involves biofeedback and electrical stimulation.
- Triple-target treatment (3T), a combination of amplitude-modulated medium-frequency stimulation and electromyographic biofeedback (EMG-BF), has shown promise.
- This study compares 3T to standard low-frequency stimulation (LFS).
Purpose of the Study:
- To compare the efficacy of 3T versus LFS in treating anal incontinence.
- To evaluate the impact of these treatments on continence and quality of life.
Main Methods:
- A multicenter randomized trial with blinded observer involving 80 patients with anal incontinence (Grade I or higher).
- Patients were randomized to receive either 3T or LFS for two 20-minute sessions daily over 6 months.
- Primary endpoint: Cleveland Clinic Score (CCS); Secondary endpoints: continence recovery and quality of life (QoL).
Main Results:
- The 3T group showed a significantly lower mean CCS (3.1 ± 4.2) compared to the LFS group (9.6 ± 3.9) after 6 months.
- 54% of patients in the 3T group regained continence, versus 0% in the LFS group (p<0.001).
- All QoL dimensions were higher in the 3T group; no major adverse effects were reported.
Conclusions:
- Triple-target treatment (3T) is superior to low-frequency stimulation (LFS) for anal incontinence.
- The combination of biofeedback and medium-frequency stimulation in 3T appears effective.
- LFS, as applied in this trial, demonstrated no significant benefit.
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