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Investigating the effect of pelvic floor biofeedback on pain and quality of life of patients with chronic coccydynia

Investigating the effect of pelvic floor biofeedback on pain and quality of life of patients with chronic coccydynia

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
IRCT
Registry ID
IRCT20250203064633N1
Enrollment
64
Registered
2025-02-15
Start date
2024-06-21
Completion date
Unknown
Last updated
2025-07-21

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Coccydynia. Sacrococcygeal disorders, not elsewhere classified

Interventions

Intervention group: Patients with coccydynia treated with Kegel exercises and 8 sessions of pelvic floor biofeedback.

Sponsors

Artesh University of Medical Sciences
Lead Sponsor

Eligibility

Sex/Gender
All
Age
18 Years to 65 Years

Inclusion criteria

Inclusion criteria: Patients with chronic coccyx pain with a VAS score equal to or greater than 4 in any of the sitting, standing or lying positions for at least 2 months, with no history of injection or manipulation of the coccyx in the past two months.

Exclusion criteria

Exclusion criteria: Absence of systemic diseases (poorly controlled diabetes, rheumatoid arthritis, etc.) No history of malignancy Absence of coccyx dislocation Absence of acute anal fissure Absence of simultaneous biofeedback treatment to treat other pelvic floor disorders There were patients who no longer wanted to continue the study

Design outcomes

Primary

MeasureTime frame
Visual Analogue Scale. Timepoint: At the beginning of the study (before the start of the intervention) and at the end of the 4th and 12th week. Method of measurement: Visual Analogue Scale.;Short form health survey 12. Timepoint: At the beginning of the study (before the start of the intervention) and at the end of the 12th week. Method of measurement: Short form health survey 12.;Dallas pain questionnaire. Timepoint: At the beginning of the study (before the start of the intervention) and at the end of the 12th week. Method of measurement: Dallas pain questionnaire.

Countries

Iran (Islamic Republic of)

Contacts

Public ContactHamidreza Matin

Artesh University of Medical Sciences

H.matin@ajaums.ac.ir+98 21 8609 6350

Outcome results

None listed

Source: IRCT (via WHO ICTRP) · Data processed: Feb 4, 2026