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Effects of Primal Reflex Release Technique on Pain, Range of Motion and Quality of Life in Post Colonoscopy Coccydynia

Effects of Primal Reflex Release Technique on Pain, Range of Motion and Quality of Life in Post Colonoscopy Coccydynia

Status
Completed
Phases
Unknown
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT07438483
Enrollment
46
Registered
2026-02-27
Start date
2025-01-06
Completion date
2025-11-02
Last updated
2026-02-27

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

Conditions

Disability and Pain Around the Coccyx, Diagnosed With Coccydynia

Keywords

Post-colonoscopy Coccydynia, Primal reflex release technique, Pain around coccyx, Numeric Pain Rating Scale

Brief summary

The study was conducted to determine the effects of primal reflex release technique on pain, range of motion and quality of life in post colonoscopy coccydynia

Interventions

Primal Reflex Release Techniques (3 sets of 10 repetitions) that includes the initial assessment to evaluate pain and Rom. PRRT techniques of coccygeal area and pelvic (10-15 minutes) And post treatment evaluation to reassess.

Standardized Physiotherapy treatment was included hot pack for 10 minutes, Hip flexors and pelvic muscles stretching for 3 times with 30 seconds and core stability exercises of pelvic tilts and bridges for 2 sets of 10 seconds. Both groups came thrice per week for a total of 4 weeks. Pre and post treatment values of both groups were analyzed.

Sponsors

Riphah International University
Lead SponsorOTHER

Study design

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

Intervention model description

A total of 46 patients were assessed for eligibility criteria by using non-probability consecutive random sampling technique. The participants were randomly allocated into two groups: Group A and Group B. Both groups received standardized as common treatment. Group A received PRRT of coccygeal area and pelvic for three times per week for a total of four weeks. Group B received standardized physiotherapy treatment three times per week for four weeks.

Eligibility

Sex/Gender
ALL
Age
18 Years to 65 Years
Healthy volunteers
No

Inclusion criteria

* Age group 18-65 year (26) * Both gender (male and female) * Diagnosed with coccydynia post colonoscopy. * Pain in and around the coccyx area without palpation, radiation and tenderness. * No history of significant trauma to the coccyx. * Difficulty in pain-free sitting for long duration.

Exclusion criteria

* Diabetes mellitus * Any malignancy * Active infection * Cyst or cancer in the pelvic region. * Previous coccygeal surgery or trauma. * Pregnancy or breastfeeding. * Major ligament injuries in the pelvic region. * Neurological disorders affecting pain perception.

Design outcomes

Primary

MeasureTime frameDescription
Numeric Pain Rate Scale (NPRS)From enrollment to the end of treatment in 10 monthsPatient's pain was summarized using numerical scale. It has numbers from 0 to 10. Where 0 is equal to "no pain" and 10 is equal to "worst pain". This scale has high test-retest reliability of r = 0.96 and 0.95, respectively.
Manual Muscle Testing (MMT)From enrollment to the end of treatment in 10 monthsManual muscle testing was used to assess muscle strength. Which can be scored using a 0-10 points using Kendal 10-point muscle strength scale. MMT is the most commonly used method for documenting impairments in muscle strength in both spine and periphery with a kappa value 0.88.

Countries

Pakistan

Contacts

PRINCIPAL_INVESTIGATORShanza Mahmood, MS-OMPT

Riphah International University

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 28, 2026