CClinicalTrials.gg
Not yet recruitingNCT07105683KCT-PLBPUpdated Aug 6, 2025

Effect of Kinetic Control Training on Postnatal Low Back Pain

An interventional study of hot pack therapy and Kinetic control training in Low Back Pain, sponsored by Cairo University. Not yet recruiting at 1 site in Egypt. Open to female participants aged 25 Years to 35 Years, including healthy volunteers. Per ClinicalTrials.gov, last updated 2025-08-06.

Sponsored by Cairo University · Not applicable, Interventional, and Treatment

From the registry’s dates

  • Primary completion was expected by Aug 2025, 1 year 1 month ago, but the record still lists the study as not yet recruiting.
Phase
Not applicable
Study type
Interventional
Enrollment
66
Allocation
Randomized
Ages
25 Years to 35 Years
Sex
Female
01

Study summary

the effect of kinetic control training and hotpack and compare it with hotpack alone on postnatal low back pain

Read the detailed description

Background: Postnatal low back pain (PLBP) is a common condition affecting women after childbirth due to musculoskeletal and biomechanical changes during pregnancy. Effective rehabilitation strategies are essential for pain relief and functional recovery.

Objective: This study aims to evaluate the effect of kinetic control training in postnatal women with low back pain.

Methods: A total of 66 postnatal women with low back pain were randomly selected from WENGAT Hospital and EL SHATBY Hospital in Alexandria. Participants were divided into two equal groups:

Group A: 33 women treated with hot pack for 20 minutes twice daily for 6 weeks. Group B: 33 women treated with a combination of kinetic control training and hot pack 3 sessions/week for 6 weeks.

Pain intensity will be assessed using the Visual Analog Scale (VAS) and Pressure Algometer. Range of motion (ROM) will be evaluated using the Modified Schober Test.

02

Conditions studied

  • Low Back Pain

Browse trials for

03

In context

Low Back Pain

2,818 studies on the registry are indexed under Low Back Pain; 482 are open to participants now.

This study's planned enrollment of 66 is close to the median of 60 across 2,268 interventional studies indexed under Low Back Pain.

Browse Low Back Pain studies →

Lead sponsor

Cairo University is the lead sponsor of 4,780 studies on the registry; 1,427 are open to participants now.

Of its 36 completed or terminated interventional studies of FDA-regulated products, 5 (14%) have results posted.

Counted across the registry records on this site, refreshed daily.

04

Who can participate

Ages eligible
25 Years to 35 Years
Sexes eligible
Female
Accepts healthy volunteers
Yes

Eligibility criteria

**Inclusion Criteria:**

  • Female patients with postnatal low back pain (PLBP) that lasted for at least 6 months.
  • Pain intensity ≥ 5 on the Visual Analog Scale (VAS).
  • Limitation score ≤ 5 on the Modified Schober Test.
  • Age between 25 and 35 years.
  • Body mass index (BMI) between 20-25 kg/m².
  • Medically stable and able to provide informed consent.
  • Positive result in the extension uncontrolled movement test, indicating:
  • Loss of lumbopelvic control.
  • Overactivity of global extensors during functional tasks. *Exclusion Criteria:**
  • Any neurological or rheumatological disorders.
  • Previous spinal surgery.
  • Pregnancy or planning to become pregnant during the study period.
  • BMI outside the 20-25 kg/m² range.
  • Inability to participate in exercise or physical activity.
05

Study design

Phase
Not applicable
Primary purpose
Treatment
Allocation
Randomized
Intervention model
Parallel assignment
Masking
Triple (Participant, Care provider, Outcomes assessor)
Enrollment
66 participants (estimated)

Study arms

  • Active comparator
    Hot Pack Therapy Only (Control Group)

    Participants in this arm receive hot pack therapy as a standard physiotherapeutic intervention. A moist hot pack is applied to the lumbar region for 20-30minutes per session, twice daily, over a period of 8weeks. This intervention is intended to provide superficial heat to reduce pain, promote muscle relaxation, and improve local circulation. No additional therapeutic exercises are administered to this group

    Other: hot pack therapy

  • Experimental
    Hot Pack Therapy + Kinetic Control Training (Experimental Group)

    Participants in this arm receive both hot pack therapy and kinetic control training. The hot pack is applied to the lumbar region for 20-30minutes per session, twice daily, for 8weeks. In addition, participants undergo kinetic control training, which includes therapist-guided exercises targeting the deep stabilizing muscles of the lumbar-pelvic region. Exercises focus on improving muscle coordination, movement control, and spinal stability. Sessions are conducted three times per week for 8 weeks.

    Other: hot pack therapy · Genetic: Kinetic control training

Interventions

  • Otherhot pack therapy

    Application of a commercial hot pack to the lumbar region for 20-30 minutes per session, twice daily, for 6 weeks.

  • GeneticKinetic control training

    is an evidence-based rehabilitation approach, focused on retraining movement patterns by addressing and improving motor control of the lumbar spine and pelvis, correcting faulty movement strategies, enhancing stability in functional tasks. The principles of KCT entail the identification of direction-specific motor control deficit, uncontrolled extension, followed by focused retraining of movement control through specific exercises designed to improve the coordination and activation of deep stabilizing muscle systems, including the transversus abdominis, multifidus, and pelvic floor muscles. This approach is especially relevant in postpartum women, where motor control deficits and poor load transfer capabilities are commonly observed . Based on the clinical presentation of patients with postnatal low back pain, demonstrated symptoms that were aggravated during lumbar extension movements or when maintaining prolonged upright postures. The

06

What researchers measure

Primary outcomes

  1. Pain Intensity Measured by Visual Analog Scale (VAS)

    Pain intensity will be assessed using the Visual Analog Scale (VAS), a validated tool for measuring subjective pain levels. Participants will indicate their pain level on a 10 cm horizontal line ranging from "no pain" (0) to "worst imaginable pain" (10). This measurement will help evaluate the effectiveness of kinetic control training in reducing postnatal low back pain compared to hot pack therapy alone

    Time frame: Baseline and after 8weeks of intervention

Secondary outcomes

  1. Lumbar Range of Motion (Flexion and Extension) Using Modified Schober Test

    This measure assesses the flexibility and mobility of the lumbar spine using the Modified Schober Test. A non-invasive tape measure method is used to evaluate the difference in spinal segment length during full flexion and extension compared to the neutral standing posture. The outcome reflects the degree of lumbar mobility, which may be affected by postnatal low back pain and improved through targeted interventions like kinetic control training.

    Time frame: Baseline and after 8weeks of intervention

07

Study locations

1 site
  • physical therapy cairo University
    Cairo, Egypt
08

References and documents

Individual participant data

Plan to share: No — The plan for sharing deidentified individual participant data is under consideration. It will depend on institutional policies and ethical approvals. Further details will be provided once finalized.

09

Updates

Tracking since Sep 25, 2026
No changes since tracking began. The registry record was last updated on Aug 6, 2025, before this site started recording changes on Sep 25, 2026. Its history is on ClinicalTrials.gov ↗
10

Registry details

Key details

Study ID
NCT07105683
Lead sponsor
Cairo University
Responsible party
Rana Ahmed Mohammed (Doctor, Cairo University) — Principal investigator
First posted
Aug 6, 2025
Start date
Aug 10, 2025 (estimated)
Primary completion
Aug 25, 2025 (estimated)
Completion
Sep 15, 2025 (estimated)
Last update
Aug 6, 2025

Study contacts

dr mohamed awad and dr marwa mahran prof and doctor, phd /master
Contact
awad18111972@yahoo.com
01224955140 ext. 01276597490
Marwa Mahran, Doctor
Contact
m.mahran2000@yahoo.com
0127 6597490
Mohammed Fawzy, Phd
principal investigator · Om el masryen hospital

Oversight

Data monitoring committee
Yes
FDA-regulated drug
No
FDA-regulated device
No
View the source record on ClinicalTrials.gov ↗

Not currently enrolling

This study is not yet recruiting, as verified in Aug 2025. You cannot join it, but the record below documents what was studied.

Follow this study

Get an email when the registry record changes — status, dates, results — or when someone posts here.

Sign in to follow

Discussion

Questions and observations about this study, from anyone following it. Not medical advice, and not a channel to the study team — their contact details are on the registry record.

Sign in to join the discussion. Reading takes no account; posting does. You choose a display name, and a pseudonym is the default.

Nothing here yet. If you are running this trial, taking part in it, or weighing whether to, this is the place to say so.

Start the discussion