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Activo, sin reclutamientoNCT07929714Registro de ClinicalTrials.gov

Kegel vs. Reverse Kegel Exercises for Coccydynia

Coccydynia

LO ESENCIAL

De qué trata este estudio

El registro no identifica actualmente este estudio como reclutando. Consulta su estado antes de planificar una evaluación.

Tipo de estudio
De intervención
Fase
No aplica
Rango de edad
18 años - 50 años
Sexo admitido
Todos los sexos
Voluntarios sanos
No aceptados
Participantes
30 Estimado

Estos son puntos de partida, no una decisión de elegibilidad. El equipo debe revisar todos los requisitos.

Las explicaciones y la navegación están en español. Los textos proporcionados por el registro, incluidos títulos, resúmenes y criterios, se conservan en su idioma original. Puedes pedir orientación en español a WCR.

Acerca de la investigación

This randomized clinical trial will compare the effects of Kegel and Reverse Kegel exercises on pain and functional disability in 30 patients with coccydynia aged 18-50 years. Participants will be randomly allocated to two groups, receiving their respective exercise protocols for 4 weeks, with three sessions per week. Outcomes will include pain intensity (NPRS), functional disability (ODI), and pain-free sitting duration, assessed at baseline, 2 weeks, and 4 weeks. Data will be analyzed using SPSS version 24.

Leer la descripción completa

Coccydynia, commonly referred to as tailbone pain, is a painful condition localized to the coccyx that significantly impairs sitting tolerance, transitional movements, and quality of life. The condition is five times more prevalent in females due to anatomical differences and the effects of obstetric trauma. A key yet frequently overlooked contributor to coccydynia is pelvic floor muscle hypertonicity, in which the levator ani, coccygeus, and adjacent muscles exert chronic traction on the coccyx, perpetuating pain and functional disability. Physical therapy, particularly pelvic floor rehabilitation, has emerged as a cornerstone of conservative management. Kegel exercises, which involve concentric contraction of the pubococcygeus and levator ani muscles, strengthen the pelvic floor and improve structural support around the coccyx. Conversely, Reverse Kegel exercises emphasize eccentric lengthening and relaxation of the pelvic floor musculature, addressing the hypertonicity directly implicated in coccydynia. Despite growing evidence for both modalities, no randomized controlled trial to date has directly compared their effects on pain and functional disability in coccydynia patients.

This study will be a randomized clinical trial comparing the effects of Kegel exercises (Group A) versus Reverse Kegel exercises (Group B) on pain and functional disability in patients diagnosed with coccydynia. Pain will be measured using the Numeric Pain Rating Scale (NPRS), functional disability using the Oswestry Disability Index (ODI), and pain-free sitting duration as a timed functional outcome measure. A sample of 30 patients (15 per group), aged 18-50 years, will be recruited using non-probability consecutive sampling and randomly allocated to groups. Both groups will receive their respective pelvic floor exercise protocols for 4 weeks (3 sessions per week, 12 sessions total). Outcome measures will be recorded at baseline, 2nd week, and 4th week. Data will be analyzed using SPSS version 24.

¿Quién podría participar?

La lista siguiente contiene el texto del patrocinador. Puede incluir condiciones, tratamientos previos, resultados de pruebas y otros requisitos. Aparecer en tu búsqueda no significa que califiques.

Inclusion Criteria:

  • Age 18-50 years, both genders. Confirmed diagnosis of coccydynia. Baseline NPRS score of 4-6. Symptoms persisting for ≥4 weeks. BMI \< 30 kg/m².

Exclusion Criteria:

Previous coccygeal or spinal surgery. Coccygeal fracture, tumor, or infection. Current pregnancy. Lower-limb neurological deficits. Pelvic organ prolapses or previous pelvic surgery. Corticosteroid injection within the past 3 months or concurrent pelvic/lumbar physiotherapy.

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Tratamiento, grupos y participación

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Asignación
Asignación al azar
Enmascaramiento
Enmascaramiento simple
Kegel Exercises (Pelvic Floor Strengthening)

THIS GROUP will receive their respective exercise protocols over 4 weeks (3 sessions per week, 12 sessions total).

Other: KEGEL EXERCISES (Pelvic Floor Strengthening)

Reverse Kegel Exercises (Pelvic Floor Relaxation)

THIS group will receive their respective exercise protocols over 4 weeks (3 sessions per week, 12 sessions total).

Other: REVERSE KEGEL EXERCISES (Pelvic Floor Relaxation)

KEGEL EXERCISES (Pelvic Floor Strengthening) OTHER

Patients in Group A will perform pelvic floor contraction exercises as follows:

Starting position: Supine lying with knees bent and feet flat, or comfortable sitting on a firm chair. Technique: Patient is instructed to identify pelvic floor muscles by attempting to stop the flow of urine midstream (without performing this during actual urination). The contraction is described as a "squeeze and lift" of the pelvic floor. Protocol: Hold contraction for 5-10 seconds, then fully relax for equal duration. Perform 10 repetitions per set, 3 sets per session, with 60- second rest intervals between sets. Progression: Contraction hold time will be increased from 5 seconds (weeks 1-2) to 10 seconds (weeks 3-4) as muscle endurance improves. Total session duration: approximately 25-30 minutes.

REVERSE KEGEL EXERCISES (Pelvic Floor Relaxation) OTHER

Patients in Group B will perform pelvic floor eccentric relaxation exercises as follows:

Starting position: Supine lying, knees bent; or "happy baby" position (supine, knees drawn toward chest with feet facing ceiling) to facilitate pelvic floor lengthening.

Technique: Patient is guided to differentiate between pelvic floor contraction and relaxation. The Reverse Kegel involves a gentle, controlled "downward bearing out" or "expansion" of the pelvic floor, as though gently pushing the floor downward and outward on inhalation. This is the opposite of Kegel contraction. Protocol: Inhale slowly and allow pelvic floor to fully descend and elongate (2-3 seconds), hold the relaxed position for 5 seconds, then exhale and allow gentle passive recoil (no active contraction). Perform 10 repetitions per set, 3 sets per session, with 60- second rest intervals between sets. Biofeedback cueing will be used (verbal and palpatory) to confirm correct muscle release rather than inadvertent contraction

Prepara tus preguntas

Qué evalúan los investigadores

Estas medidas indican qué se estudia. No prueban que un tratamiento funcione.

Medidas principales

NPRS

Plazo: BASELINE AND AFTER 2 AND 4 WEEKS

NPRS 11-point numeric with 0 representing No pain, 1-3 representing Mild Pain (nagging, annoying, interfering little with ADLs), 4-6 representing Moderate Pains (interferes significantly with ADLs), 7-10 representing Sever Pain (disabling, unable to perform

ODI (Oswestry Disability Index)

Plazo: BASELINE AND AFTER 2 AND 4 WEEKS

Assesses functional disability related to pain through a questionnaire covering daily activities.

TSTT (Timed Sitting Tolerance Test)

Plazo: BASELINE AND AFTER 2 AND 4 WEEKS

Measures the duration a patient can tolerate sitting before pain requires them to stop or change position.

El registro no indica resultados publicados.

Revisa las tablas completas y sus limitaciones en el registro oficial.

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Centros de investigación (1)

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1 centros

UMTLahore, Punjab Province, PakistanEstado desconocido

Equipo y fechas

Patrocinador principal
University of Management and Technology Lahore
Inicio del estudio
5 nov 2026 Real
Finalización primaria
31 dic 2026 Estimado
Finalización del estudio
31 dic 2026 Estimado
Primera publicación
10 nov 2026 Real
Última actualización
10 nov 2026 Real

Contactos oficiales del estudio

No hay un contacto central indicado. Revisa los centros y el registro oficial.

Título oficial del estudio

Comparative Effect of Kegel and Reverse Kegel Exercises on Pain and Functional Disability in Patients With Coccydynia

EL PRÓXIMO PASO, CON APOYO HUMANO

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Fuente: API v2 de ClinicalTrials.gov. Patrocinadores e investigadores envían la información. La NLM no aprueba la seguridad ni la ciencia de todos los estudios registrados. Aviso del registro.

Consultado: 12 nov 2026 · Última actualización del registro: 10 nov 2026