Maitland Mobilization and Lumbopelvic Coordination Exercises in Patients With Post Colonoscopy Coccydynia .

February 23, 2026 updated by: Riphah International University

Combined Effects of Maitland Mobilization and Lumbopelvic Coordination Exercises on Pain, Range of Motion and Quality of Life in Patients With Post Colonoscopy Coccydynia .

The study was conducted to determine the Combined effects of Maitland mobilization and lumbopelvic coordination exercise on pain, range of motion and quality of life in patients with post colonoscopy coccydynia.

Study Overview

Status

Completed

Conditions

Intervention / Treatment

Study Type

Interventional

Enrollment (Actual)

42

Phase

  • Not Applicable

Contacts and Locations

This section provides the contact details for those conducting the study, and information on where this study is being conducted.

Study Locations

  • Pakistan
    • Punjab Province
      • Multan Khurd, Punjab Province, Pakistan, 60810
        • Ali Rehabilitation and Pain relieve center Multan

Participation Criteria

Researchers look for people who fit a certain description, called eligibility criteria. Some examples of these criteria are a person's general health condition or prior treatments.

Eligibility Criteria

Ages Eligible for Study

  • Adult

Accepts Healthy Volunteers

No

Description

INCLUSION CRITERIA

  • Males and Females between 18 to 60
  • Diagnosed with post colonoscopy coccydynia
  • Pain in the lower back and around coccyx area without palpation and radiation
  • Pain level of 3 at the scale of 10
  • No history of trauma to the coccyx
  • Ability to participate in the study

EXCLUSION CRITERIA

  • Present of neurological disorders
  • Any trauma or surgery
  • Pregnancy
  • Cyst or cancer in the pelvic region
  • Diabetes mellitus
  • Major ligament injuries in the pelvic region
  • Any type of fractures
  • Diagnosed psychological disorders

Study Plan

This section provides details of the study plan, including how the study is designed and what the study is measuring.

How is the study designed?

Design Details

  • Primary Purpose: Treatment
  • Allocation: Randomized
  • Interventional Model: Parallel Assignment
  • Masking: Single

Arms and Interventions

Participant Group / Arm
Intervention / Treatment
Experimental: Maitland mobilization and lumbopelvic coordination exercises
Other: Maitland Mobilization and lumbopelvic coordination
group A received maitland mobilization technique 3 times per week which aimed to reduce pain and improve overall mobility and function . Intervention involve streching the hip flexors muscles (ilipsoas, rectus femoris ,sartorius) performed as 2sets of 30seconds. strengthening exercises such as pelvic tilts and bridges were performed using 3 sets of 10 repetitions.
Active Comparator: Standard Physical Therapy
Other: Standard physical therapy treatment
group B was given hot pack for 10min to reduce pain and promote tissue relaxation followed by stretching of the superficial and coccygeal muscles around the pelvis and lower back performed 3 times for 30 sec each.

What is the study measuring?

Primary Outcome Measures

Outcome Measure
Measure Description
Time Frame
numeric pain scale
Time Frame: from enrollment to 4 sessions per week for total duration of 4 week
the scale was used to determine the patient level of pain . the range of this scale is from 0 to 10. no pain is represented by ''O"'and worst pain is represented by ''10''.
from enrollment to 4 sessions per week for total duration of 4 week
inclinometer
Time Frame: from enrollment to 4 sessions per week to total duration of 4 weeks.
The range of motion will be measured using inclinometer that has an inter-rater reliability (ICC2,2 = 0.92 to 0.96) and in case of coccydynia, the range of motion will be assessed in the sacroiliac joint, lumbar spine and pelvic region
from enrollment to 4 sessions per week to total duration of 4 weeks.
SF 36 questionnaire
Time Frame: from enrollement to 4 sessions per week for total duration of 4 weeks.
One of the most widely used tools for assessing health-related quality of life is the 36-item Short Form Health Survey (SF-36). Physical functioning (10 items), physical role limitations (4 items),bodily pain (2 items), general health perceptions (5 items), energy/vitality (4 items), social functioning (2 items), and emotional role limitations (3 items) are the eight domains of health status that are measured by the 36-item SF-36 scale
from enrollement to 4 sessions per week for total duration of 4 weeks.

Collaborators and Investigators

This is where you will find people and organizations involved with this study.

Sponsor

Riphah International University

Investigators

  • Principal Investigator: iqra ghafoor, Ph.D*, Riphah International University

Publications and helpful links

The person responsible for entering information about the study voluntarily provides these publications. These may be about anything related to the study.

General Publications

Study record dates

These dates track the progress of study record and summary results submissions to ClinicalTrials.gov. Study records and reported results are reviewed by the National Library of Medicine (NLM) to make sure they meet specific quality control standards before being posted on the public website.

Study Major Dates

Study Start (Actual)

February 3, 2025

Primary Completion (Actual)

November 3, 2025

Study Completion (Actual)

November 11, 2025

Study Registration Dates

First Submitted

February 23, 2026

First Submitted That Met QC Criteria

February 23, 2026

First Posted (Actual)

February 27, 2026

Study Record Updates

Last Update Posted (Actual)

February 27, 2026

Last Update Submitted That Met QC Criteria

February 23, 2026

Last Verified

February 1, 2026

More Information

Terms related to this study

Keywords

Additional Relevant MeSH Terms

Other Study ID Numbers

  • REC/RCR&AHS/24/01115

Plan for Individual participant data (IPD)

Plan to Share Individual Participant Data (IPD)?

NO

Drug and device information, study documents

Studies a U.S. FDA-regulated drug product

No

Studies a U.S. FDA-regulated device product

No

This information was retrieved directly from the website clinicaltrials.gov without any changes. If you have any requests to change, remove or update your study details, please contact register@clinicaltrials.gov. As soon as a change is implemented on clinicaltrials.gov, this will be updated automatically on our website as well.

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