Comparison of effects of mobilization with movement at Sacroiliac joint with and without Postero-Anterior Glide at L5-S1 in patients with Sacroiliac joint dysfunction

Effects of mobilization with movement at Sacroiliac joint with and without Postero-Anterior Glide at L5-S1 in patients with Sacroiliac joint dysfunction

Status

Active, not recruiting

Phases

Unknown

Study type

Interventional

Source

IRCT

Registry ID

IRCT20200527047582N1

Enrollment

Registered

2020-07-21

Start date

2019-11-05

Completion date

Unknown

Last updated

2020-08-17

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

Conditions

sacroiliac joint dysfunction.

Interventions

Intervention 1: Intervention group 1: Mobilisation with movement at Sacroiliac joint dysfunction with Poster-anterior glide at L5-S1. After taking consent 3 sessions per week will be given to the pati

Eligibility

Sex/Gender

All

Age

25 Years to 49 Years

Inclusion criteria

Inclusion criteria: Patients who had an acute unilateral or bilateral SIJ syndrome during the past 6 weeks. Those in whom the level of pain over the previous 24 h increased Patients having no manipulative treatment within the past month. Pain and tenderness at SIJ FABER, compression, distraction, and Gaenslen's. provocation tests POSITIVE

Exclusion criteria

Exclusion criteria: Previous spinal manipulative treatment Having pain and discomfort in the lumbar spine Destructive lesions of the spine, ribs and pelvis cauda equina syndrome Patients having gross instability or active infection Pregnancy, Spondylolysthesis, and previous back surgery.

Design outcomes

Primary

Measure	Time frame
Pain. Timepoint: before intervention, after intervention , after 2 weeks and after one month. Method of measurement: Numeric pain rating scale (NPRS): NPRS is anchored by terms describing pain severity extremes. The 11-point numeric scale ranges from '0' representing one pain extreme (e.g. “no pain”) to '10' representing the other pain extreme (e.g. “pain as bad as you can imagine” or “worst pain imaginable”).	—

Measure

Time frame

Pain. Timepoint: before intervention, after intervention , after 2 weeks and after one month. Method of measurement: Numeric pain rating scale (NPRS): NPRS is anchored by terms describing pain severity extremes. The 11-point numeric scale ranges from '0' representing one pain extreme (e.g. “no pain”) to '10' representing the other pain extreme (e.g. “pain as bad as you can imagine” or “worst pain imaginable”).

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Secondary

Measure	Time frame
Disability. Timepoint: Subjects will be reassessed by researcher immediately after treatment, after 2 weeks and after one month. Treatment sessions (3 session a week) will be given to the subjects. Method of measurement: Oswestry Disability Questionnaire (ODQ):It is a functional index designed to determine the symptoms and limitations that patient experiences while performing daily activities. This scale consists of 10 items in the form of activities of daily living with each item scoring from 0 to 5 where 0 is no difficulty in performing that activity and 5 is inability to do that activity. This will used for assessment of the associated disability.	—

Measure

Time frame

Disability. Timepoint: Subjects will be reassessed by researcher immediately after treatment, after 2 weeks and after one month. Treatment sessions (3 session a week) will be given to the subjects. Method of measurement: Oswestry Disability Questionnaire (ODQ):It is a functional index designed to determine the symptoms and limitations that patient experiences while performing daily activities. This scale consists of 10 items in the form of activities of daily living with each item scoring from 0 to 5 where 0 is no difficulty in performing that activity and 5 is inability to do that activity. This will used for assessment of the associated disability.

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Countries

Pakistan

Contacts

Public ContactHufsa Tariq

Riphah international university

hufsa.tariq5@gmail.com+92 42 36603199

Outcome results

None listed

Source: IRCT (via WHO ICTRP) · Data processed: Feb 4, 2026