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Effect of Manipulation on Coccydynia

The Effectiveness of Manipulation in Combination With Exercise for Patients With Coccydynia: A Randomized Controlled Trial

Status
Completed
Phases
NA
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT05917366
Enrollment
46
Registered
2023-06-23
Start date
2022-07-16
Completion date
2023-05-20
Last updated
2023-06-23

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

Conditions

Coccyx Disorder, Pelvic Floor; Weak, Stretch

Brief summary

The aim of this study was to investigate the efficacy of manipulation combined with exercise as a treatment for patients with coccydynia.

Detailed description

Subject: Coccydynia is a painful condition characterized by inflammation and discomfort in the coccyx region, commonly known as the tailbone. It can significantly affect an individual's quality of life by impairing their ability to sit, stand, or engage in daily activities. Various treatment approaches have been explored to alleviate the symptoms of coccydynia, including manipulation techniques and exercise interventions. However, to date, there is a scarcity of research investigating the combined effects of manipulation and exercise for patients with coccydynia. Purpose: The purpose of this study is to evaluate the efficacy of combining manipulation techniques with exercise interventions for patients diagnosed with coccydynia, a painful condition affecting the coccyx region. Despite the debilitating impact of coccydynia on daily activities and quality of life, there is a limited understanding of the optimal treatment approach for this condition. This study aims to address this knowledge gap by investigating the potential benefits of combining manipulation and exercise in managing coccydynia.

Interventions

OTHERExercises

Stretching exercise for the piriformis and iliopsoas muscles. strengthening exercises for pelvic floor muscles

OTHERCoccyx Manipulation

Application of manipulation to relax the levetor ani muscle

Sponsors

KTO Karatay University
Lead SponsorOTHER

Study design

Allocation
RANDOMIZED
Intervention model
PARALLEL
Primary purpose
TREATMENT
Masking
DOUBLE (Subject, Investigator)

Eligibility

Sex/Gender
ALL
Age
25 Years to 60 Years
Healthy volunteers
No

Inclusion criteria

* chronic (3 months) coccydynia * age over 25 and under 60 years * no ongoing antidepressant treatment * no medicolegal litigation or occupational-accident etiology

Exclusion criteria

* undergoing an operation aimed at the anal area * those with additional diseases such as radiculopathy etc.

Design outcomes

Primary

MeasureTime frameDescription
Change from baseline in Pain at 4 weeks and 6 monthsBaseline measurement before the treatment programs begin (pre-intervention), post-intervention at week 4, and 6 months follow-upA visual analog scale (VAS) numbered 0-10 will be used in the assessment of pain.
Change from baseline in Paris questionnaire at 4 weeks and 6 monthsBaseline measurement before the treatment programs begin (pre-intervention), post-intervention at week 4, and 6 months follow-upCoccydynia-related symptoms were recorded using the Paris questionnaire, ranging from 0 (no symptoms) to 10 (maximum symptoms). The Paris questionnaire is a specific assessment tool designed to evaluate symptoms and functional limitations related to coccydynia, a condition characterized by pain in the coccyx region. The questionnaire consists of a series of questions that inquire about the severity and impact of coccyx pain on various activities and daily life.
Change from baseline in The Oswestry Disability Index at 4 weeks and 6 monthsBaseline measurement before the treatment programs begin (pre-intervention), post-intervention at week 4, and 6 months follow-upThe Oswestry Disability Index consists of ten sections, each addressing a different aspect of functional ability, including pain intensity, lifting, ability to walk, ability to sit, ability to stand, sleep quality, ability to socialize, ability to travel, ability to perform self-care tasks, and ability to perform household tasks. Each section contains multiple statements, and the individual rates their level of disability on a scale of 0 to 5, with higher scores indicating greater disability.

Countries

Turkey (Türkiye)

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 4, 2026