Effect of Coccygeal Mobilization in Female With Coccydynia

Trial statusNot yet recruiting
Trial phaseNot applicable
Trial typeInterventional
Biological sexFemale
Age35-45
SponsorRiphah International University

About this trial

Aim of the study to evaluate the impact of mobilization on symptom severity, disability \& quality of life in female with Coccydynia.

Eligibility criteria

This trial does not accept healthy volunteers

Qualifiers

Patient with coccygeal pain for more than 3 months

Diagnosed patients of Coccydynia.

Pain from the pericoccygeal soft tissues

Pelvic floor muscle spasm, referred pain from lumbar pathology.

Disqualifiers

Patient with local infection (inflammatory bowel disease or psoriasis)

Patient who undergone cocygectomy, sacroccygeal joint fusion, bleeding disorder and pregnancy.

Spinal surgery

Fracture of coccyx

Trial design

Design model

Parallel

Treatments tested in this trial

  • external mobilization

    Other intervention

    two 5-minute sessions of external manipulation per week over a 5-week period.

  • rectal coccygeal mobilization

    Other intervention

    consisted of two 5-minute sessions of external manipulation per week over a 5-week period.

Treatment groups

34 Participants
are divided into 2 treatment groups
Group A: (external coccygeal mobilization+ stretchingExperimental treatment 1 intervention
Group B: internal coccygeal mobilization+ stretchingActive comparator 1 intervention

Trial outcomes

Primary outcomes

1

Paris Scale Questionnaire

The Paris Questionnaire was specifically designed for coccydynia. It covers, specifically, the functional aspects of the pain, which are not assessed by the other two questionnaires. It explores the pain when sitting (and differs, in this respect, from the VAS, which only measures the intensity of the pain), when passing from sitting to standing (very specific of coccydynia with radiologic findings), when walking and at night (pain on these occasions is frequent in severe coccydynia), and when traveling (the most sensitive detector of coccygeal pain). This set of three questionnaires offers a correct representation of the pain impact in chronic coccydynia.

Time frame
4th week
2

DALLAS Pain Questionnaire

The Dallas Pain Questionnaire (DPQ), which is a 16-item visual analog tool was developed by Lawlis, McCoy, and Selby (appendix) for the purpose of evaluating subject's cognitions about the percentage that chronic pain affects four aspects of the patients' lives: 1) daily activities including pain and intensity, personal care, lifting, walking, sitting, standing, and sleeping; 2) work and leisure activities including social life, travelling, and vocational; 3) anxiety-depression and 4) social interest that includes interpersonal relationship, social support, and punishing responses. Each question asks the responder to rate their experience with different activities using a percentage scale from 0% to 100%. Retest reliability of DALLAS Pain Questionnaire is 0.970.

Time frame
4th week
3

SF-36 Questionnaire in Urdu version

The SF-36-U is a 36 item scale, which measures eight domains of health status: physical functioning (10 items); physical role limitations (four items); bodily pain (two items); general health perceptions (five items); energy/vitality (four items); social functioning (two items); emotional role limitations (three items) and mental health (five items). A scoring algorithm is used to convert the raw scores into the eight dimensions listed above. The scores are transformed to range from zero where the respondent has the worst possible health to 100 where the respondent is in the best possible health. SF-36-U presented good to excellent test-retest reliability for all eight domains (ICC2,1 = 0.75-0.92. Internal consistency for all domains (Cronbach's alpha = 0.73- 0.90)

Time frame
4th week

Secondary outcomes

Other outcomes

Sponsors and contacts

Click on the lead sponsor to view all of their trials.

This trial is not recruiting at the moment. You can still explore other options: