ClinicalTrials.gg
Active, not recruitingNCT07929714Updated Nov 10, 2026

Kegel vs. Reverse Kegel Exercises for Coccydynia

An interventional study of KEGEL EXERCISES (Pelvic Floor Strengthening) and REVERSE KEGEL EXERCISES (Pelvic Floor Relaxation) in Coccydynia, sponsored by University of Management and Technology Lahore. Active, not recruiting at 1 site in Pakistan. Open to participants aged 18 Years to 50 Years. Per ClinicalTrials.gov, last updated 2026-11-10.

Sponsored by University of Management and Technology Lahore · Not applicable, Interventional, and Treatment

Updated Nov 10, 2026Newly registeredGo to Updates ↓
Phase
Not applicable
Study type
Interventional
Enrollment
30
Allocation
Randomized
Ages
18 Years to 50 Years
Sex
All
01

Study summary

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.

Read the detailed description

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.

02

Conditions studied

  • Coccydynia

Keywords

  • Kegel exercises,
  • Reverse Kegel exercises,
  • pelvic floor rehabilitation,
  • NPRS,
  • Oswestry Disability Index.
03

In context

Lead sponsor

University of Management and Technology Lahore is the lead sponsor of 39 studies on the registry; 20 are open to participants now.

Counted across the registry records on this site, refreshed daily.

04

Who can participate

Ages eligible
18 Years to 50 Years
Sexes eligible
All
Accepts healthy volunteers
No

Go through the criteria one by one — yes, no or not sure — and take the list to your doctor or the study team. Kept in this browser only.

Inclusion criteria

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

Exclusion criteria

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. injection within the past 3 months or concurrent pelvic/lumbar physiotherapy.

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Terms in these criteria, in plain language(2)

Underlined terms in the criteria open these too. Explained by clinicaltrials.gg, not part of the registry record. The study team decides who can take part.

BMI (body mass index)

Weight in kilograms divided by height in metres squared. Example: 70 kg and 1.75 m gives 70 ÷ (1.75 × 1.75) ≈ 22.9.

What counts as overweight or obesity differs between countries (some use lower cut-offs), so go by the range the study states.

Corticosteroids (steroids)

Anti-inflammatory medicines such as prednisone, prednisolone and dexamethasone — not the anabolic steroids used for muscle.

Studies differ in what they allow: check which steroid medicines, routes (tablets, injections, creams, inhalers, eye drops) and doses this study accepts.

05

Study design

Phase
Not applicable
Primary purpose
Treatment
Allocation
Randomized
Intervention model
Parallel assignment
Masking
Single (Outcomes assessor)
Enrollment
30 participants (estimated)

Study arms

  • Experimental
    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)

  • Active comparator
    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)

Interventions

  • OtherKEGEL EXERCISES (Pelvic Floor Strengthening)

    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.

  • OtherREVERSE KEGEL EXERCISES (Pelvic Floor Relaxation)

    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

06

What researchers measure

Primary outcomes

  1. NPRS

    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

    Time frame: BASELINE AND AFTER 2 AND 4 WEEKS

  2. ODI (Oswestry Disability Index)

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

    Time frame: BASELINE AND AFTER 2 AND 4 WEEKS

  3. TSTT (Timed Sitting Tolerance Test)

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

    Time frame: BASELINE AND AFTER 2 AND 4 WEEKS

07

Study locations

1 site
  • UMT
    Lahore, Punjab Province 54000, Pakistan
08

References and documents

Individual participant data

Plan to share: Yes — The results data collected , de-identified individual participant data will be shared.

Supporting information: Study protocol, Statistical analysis plan, Informed consent form

Time frame: 6 months after the publication of the manuscript

Access criteria: The data can be requested from the corresponding author.

No publications or documents are linked to this record.

09

Updates

1 registry update since Sep 25, 2026
Registered
First appeared on the registry. No changes since
Nov 10, 2026
Show all 1 update
  1. Nov 10, 2026
    First appeared on the registry

From the registry record's own update history. This site started tracking changes on Sep 25, 2026; for anything earlier, see the record history on ClinicalTrials.gov ↗

10

Registry details

Key details

Study ID
NCT07929714
Lead sponsor
University of Management and Technology Lahore
Responsible party
Tamknat Ilyas (ASSISTANT PROFESSOR, University of Management and Technology Lahore) — Principal investigator
First posted
Nov 10, 2026
Start date
Nov 5, 2026
Primary completion
Dec 31, 2026 (estimated)
Completion
Dec 31, 2026 (estimated)
Last update
Nov 10, 2026

Oversight

Data monitoring committee
Yes
FDA-regulated drug
No
FDA-regulated device
No
View the source record on ClinicalTrials.gov ↗

Not currently enrolling

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