NCT06737900

Brief Summary

The goal of this randomized clinical trial is to learn if the given interventions that is jandas approach versus Proprioceptive Neuromuscular Facilitation technique can treat pain, disability, range of motion, endurance and quality of life in patients with Lower cross syndrome on both genders and age group of 25-40 years. The main questions it aims to answer are: Does jandas approach versus Proprioceptive neuromuscular facilitation technique improves pain, disability, range of motion, endurance and quality of life in patients with lower cross syndrome? There is a comparison between two groups: Researchers will compare the jandas approach and proprioceptive neuromuscular facilitation technique to see if there is effects on pain, disability, range of motion, endurance and quality of life in patients with lower cross syndrome. Participants in group A will be given

  • Heating pad for 10 minutes
  • Core stability exercises for 20 minutes with 10 seconds of rest intervals
  • Proprioceptive Neuromuscular Facilitation technique was used for stretching of erector spinae, quadratus lumborum, rectus femoris and iliopsoas and rhythmic stabilization technique for strengthening. Stretching was performed using contract-relax technique in supine, prone and side lying positions. The Contract-Relax method included the target muscle to be lengthened and held in lengthened position while the patient contracted the Target-Muscle to its maximum position isometrically 3 to 6 seconds.
  • Rhythmic stabilization technique was used to strengthen and stabilize the postural trunk muscles of hip: Abdominals and gluteal muscles strengthening and Participants in group B will be given
  • Heating pad for 10 minutes
  • Core stability exercises for another 20 minutes.
  • After which it was treated with the Janda's approach of musculoskeletal pain that includes strengthening of the weakened muscles and stretching of the tightened muscles including Stretching exercise for erector spinae and back extensors muscles Stretching exercises for iliopsoas muscle and rectus femoris muscle Strengthening exercise for abdominal muscle and gluteal maximus muscle

Trial Health

57
Monitor

Trial Health Score

Automated assessment based on enrollment pace, timeline, and geographic reach

Trial has exceeded expected completion date
Enrollment
52

participants targeted

Target at P25-P50 for not_applicable

Timeline
Completed

Started Jul 2024

Shorter than P25 for not_applicable

Geographic Reach
1 country

1 active site

Status
recruiting

Health score is calculated from publicly available data and should be used for screening purposes only.

Trial Relationships

Click on a node to explore related trials.

Study Timeline

Key milestones and dates

Study Start

First participant enrolled

July 1, 2024

Completed
5 months until next milestone

Primary Completion

Last participant's last visit for primary outcome

December 1, 2024

Completed
11 days until next milestone

First Submitted

Initial submission to the registry

December 12, 2024

Completed
5 days until next milestone

First Posted

Study publicly available on registry

December 17, 2024

Completed
15 days until next milestone

Study Completion

Last participant's last visit for all outcomes

January 1, 2025

Completed
Last Updated

December 17, 2024

Status Verified

December 1, 2024

Enrollment Period

5 months

First QC Date

December 12, 2024

Last Update Submit

December 16, 2024

Conditions

Keywords

Disability, Muscle strength, Pain, Quality of life, range of motion

Outcome Measures

Primary Outcomes (2)

  • numerical pain rating scale

    changes from baseline numerical pain rating scale is a scale that was used to measure pain of the patient and ranges from 0 to 10. 0 gives an indication of no pain and 10 gives an indication of worst pain.

    4th day

  • owestry disability index

    changes from baseline in functional impairment and disability, Owestry Disability Index was used. ODI consist of 10 items that are related to daily living activities limitation with 6 levels being set in each dimension. The score of 0 indicates the disability of lowest level, while 5 is an indication of disability of highest level. The overall score is then converted in percentage out of 100%

    4th day

Secondary Outcomes (11)

  • SF-36

    4th day

  • ROM lumber spine (flexion)

    4th day

  • ROM lumber spine (extension)

    4th day

  • ROM lumber spine (lumber right lateral flexion)

    4th day

  • ROM lumber spine (lumber left lateral flexion)

    4th day

  • +6 more secondary outcomes

Study Arms (2)

traditional physical therapy

ACTIVE COMPARATOR

Heating pad for 10 minutes and Core stability exercises for 20 minutes with 10 seconds of rest intervals.

Other: jandas approach

Proprioceptive Neuromuscular Facilitation technique

EXPERIMENTAL

Heating pad for 10 minutes and core stability exercises for 20 minutes along with Proprioceptive Neuromuscular Facilitation technique was used for stretching and rhythmic stabilization technique for strengthening. Stretching was performed using contract-relax technique.

Other: traditional physical therapy

Interventions

* Heating pad for 10 minutes * Core stability exercises for 20 minutes with 10 seconds of rest intervals * Patients were advised to stretch for 5 minutes then perform lumber stability exercises. * These stability exercises included side bridges, supine extension bridge, straight leg raise in prone lying, alternate arm and leg raise from quadruped position and prone bridges. Both groups took sessions thrice a week for a total of 4 weeks.

Proprioceptive Neuromuscular Facilitation technique

* Stretching exercise for erector spinae and back extensors muscles * Stretching exercises for iliopsoas muscle and rectus femoris muscle * Strengthening exercise for abdominal muscle and gluteal maximus muscle Stretching exercise was performed actively for 3 repetitions x 1 set and 4 days a week Strengthening exercise was performed for 10 second hold and 10 repetitions. All Exercises was performed 3 times per week for total of 4 weeks

traditional physical therapy

Eligibility Criteria

Age25 Years - 40 Years
Sexall
Healthy VolunteersNo
Age GroupsAdult (18-64)

You may qualify if:

  • Age group of 25-40 years.
  • Both genders male and female.
  • NPRS score range from 4-7.
  • Modified Thomas test positive , Back extensor test positive, prone hip extension strength test positive , Trunk flexion strength test positive.

You may not qualify if:

  • Vertebral Fractures
  • Tumors
  • Pregnancy
  • Diagnosed psychological disorders

Contact the study team to confirm eligibility.

Sponsors & Collaborators

Study Sites (1)

Riphah Rehab Training and Research Center

Lahore, Punjab Province, 54000, Pakistan

RECRUITING

Related Publications (1)

  • 1) authors: rajalaxmi v, nandhini g etc, article name: efficacy of jandas approach versus brueggers exercise in pelvic cross syndrome and its impact on quality of life, journal name: JK welfare and pharmascope foundation, publication date: 8 feb 2020, volume and pages were not mentioned

    BACKGROUND

MeSH Terms

Conditions

Pain

Condition Hierarchy (Ancestors)

Neurologic ManifestationsSigns and SymptomsPathological Conditions, Signs and Symptoms

Study Officials

  • Amna Shahid, t-DPT

    Riphah International University

    PRINCIPAL INVESTIGATOR

Central Study Contacts

Study Design

Study Type
interventional
Phase
not applicable
Allocation
RANDOMIZED
Masking
DOUBLE
Who Masked
PARTICIPANT, INVESTIGATOR
Purpose
TREATMENT
Intervention Model
PARALLEL
Model Details: there were total of 52 participants and were randomly assigned to two different groups. Group A received proprioceptive neuromuscular facilitation technique and Group B received jandas approach of stretching and strengthening. The aim of this study was to study the Effects of Jandas approach versus Proprioceptive Neuromuscular Facilitation technique on pain, disability, range of motion, endurance and quality of life in patients with lower crossed syndrome
Sponsor Type
OTHER
Responsible Party
SPONSOR

Study Record Dates

First Submitted

December 12, 2024

First Posted

December 17, 2024

Study Start

July 1, 2024

Primary Completion

December 1, 2024

Study Completion

January 1, 2025

Last Updated

December 17, 2024

Record last verified: 2024-12

Data Sharing

IPD Sharing
Will not share

Locations