ClinicalTrials.gg
Not yet recruitingNCT07682142LLA-HTUpdated Jul 6, 2026

Hamstring Tightness and Lumbar Lordosis Angel Across Functional Sitting Posture.

An observational study in Hamstring Tightness, Lumbar Lordosis and Sedentary Behavior, sponsored by Cairo University. Not yet recruiting at 1 site in Egypt. Open to participants aged 18 Years to 45 Years, including healthy volunteers. Per ClinicalTrials.gov, last updated 2026-07-06.

Sponsored by Cairo University · Observational

Study type
Observational
Model
Cohort
Time perspective
Cross-sectional
Enrollment
110
Ages
18 Years to 45 Years
Sex
All
01

Study summary

The goal of this observational study is to learn about the relationship between hamstring tightness and the lumbar lordosis angle in sedentary adults across different sitting postures. The main question it aims to answer is:

Is hamstring tightness related to the lumbar lordosis angle across three functional sitting postures (upright, slumped, and forward-leaning)? It also asks whether hamstring tightness differs between men and women, whether it differs between the dominant and non-dominant leg, and whether the lumbar lordosis angle differs between men and women across the three postures.

Participants will have their hamstring tightness measured with the Active Knee Extension test and their lumbar lordosis angle measured with a bubble inclinometer while sitting in each of the three postures.

Read the detailed description

Prolonged sitting is a defining feature of contemporary sedentary lifestyles and an established risk factor for musculoskeletal disorders of the lumbar spine. During sustained sitting, the hip is held in flexion and the hamstring muscle-tendon unit is maintained in a shortened position, which over time is associated with reduced hamstring extensibility (hamstring tightness). Because the hamstrings originate from the ischial tuberosity, a loss of hamstring extensibility exerts a posteriorly directed pull on the pelvis, promoting posterior pelvic tilt. Through regional spinopelvic coupling, this change in pelvic orientation alters the sacral slope and, consequently, the lumbar lordosis angle.

Although the relationship between hamstring tightness and lumbar lordosis has been described previously, most existing studies have evaluated it in the standing position. Sedentary individuals, however, spend the majority of their day seated, where the line of gravity, baseline muscle activity, and passive tissue demands placed on the spine differ substantially from those in standing. Evidence is therefore limited regarding how hamstring tightness relates to the lumbar lordosis angle across the functional sitting postures encountered in daily life, and regarding how this relationship may vary by sex and between the dominant and non-dominant lower limb.

This cross-sectional observational study will be conducted on 110 sedentary adults (55 male and 55 female), aged 18 to 45 years, recruited according to predefined eligibility criteria. The sample size was determined using G*Power based on a bivariate-normal correlation model. Eligible participants will be sedentary (more than six hours of sitting per day and a physical-activity level below 600 MET-minutes/week on the International Physical Activity Questionnaire), with a body mass index below 30 kg/m², bilateral hamstring tightness, and no current low back pain or other exclusionary conditions.

Following screening and informed consent, each participant's demographic and anthropometric data will be recorded, and lower-limb dominance will be determined using a three-task behavioral battery. Hamstring tightness will be assessed bilaterally using the Active Knee Extension (AKE) test, recorded with a digital goniometer, with the mean of three trials used for analysis. The lumbar lordosis angle (T12-S2) will be measured using a double bubble inclinometer in three randomized functional sitting postures-upright, slumped, and forward-leaning-with the mean of three trials per posture used for analysis.

The primary aim is to examine the correlation between hamstring tightness and the lumbar lordosis angle in each of the three sitting postures. The secondary aims are to compare hamstring tightness between male and female participants, to compare hamstring tightness between the dominant and non-dominant lower limb, and to compare the lumbar lordosis angle between male and female participants across the three postures. Data will be analyzed using Pearson correlation coefficients, independent- and paired-samples t-tests, and a mixed-design analysis of variance, with the significance level set at p \< 0.05.

02

Conditions studied

  • Hamstring Tightness
  • Lumbar Lordosis
  • Sedentary Behavior
  • Posture Sitting Position

Keywords

  • Hamstring tightness
  • Lumbar lordosis
  • Sitting posture
  • Functional sitting postures
  • Sedentary adults
  • Active Knee Extension test
  • AKE test
  • bubble inclinometer
  • Pelvic tilt
  • Lumbopelvic rhythm
  • Limb dominance
  • Posterior pelvic tilt
  • Spinopelvic alignment
03

In context

Lordosis

30 studies on the registry are indexed under Lordosis; 5 are open to participants now.

This study's planned enrollment of 110 is above the median of 59 across 14 observational studies indexed under Lordosis.

Browse Lordosis studies →

Lead sponsor

Cairo University is the lead sponsor of 4,941 studies on the registry; 1,458 are open to participants now.

Of its 37 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
18 Years to 45 Years
Sexes eligible
All
Accepts healthy volunteers
Yes
Sampling method
Non-probability sample

Study population

Sedentary adults of both sexes, aged 18 to 45 years, recruited from the Nasser institute hospital, and the surrounding community. Eligible participants are healthy individuals with a sedentary lifestyle (more than six hours of sitting per day and a physical-activity level below 600 MET-minutes per week on the International Physical Activity Questionnaire), a body mass index below 30 kg/m², and bilateral hamstring tightness, with no current low back pain or other excluding musculoskeletal, neurological, or spinal conditions

Go through the criteria one by one — yes, no or not sure — and take the list to your doctor or the study team. Kept in this browser only.

Inclusion criteria

  • Healthy adults aged 18-45 years.
  • Sedentary occupation requiring > 6 hours of sitting per day.
  • Active Knee Extension (AKE) angle >15°.
  • Bilateral hamstring tightness.
  • Sedentary individual as determined by IPAQ (MET≤ 600 min/week).
  • Asymptomatic for low back pain at the time of testing.

Exclusion criteria

Exclusion Criteria:

  • History of significant low back pain requiring medical treatment in the past 12 months.
  • Previous spinal surgery or structural spinal deformities.
  • Lower extremity injury or surgery within the past 6 months.
  • Neurological disorders affecting sensation or movement.
  • Pregnant female or get birth in the last year.
  • (BMI) ≥ 30 kg/m².
  • postural deviations resulting from shortening of the iliopsoas and erector spinae or insufficiency of the core stabilizers and hip extensors
Terms in these criteria, in plain language(1)

Underlined terms in the criteria open these too. Explained by clinicaltrials.gg, not part of the registry record. The study team decides who can take part.

BMI (body mass index)

Weight in kilograms divided by height in metres squared. Example: 70 kg and 1.75 m gives 70 ÷ (1.75 × 1.75) ≈ 22.9.

What counts as overweight or obesity differs between countries (some use lower cut-offs), so go by the range the study states.

05

Study design

Observational model
Cohort
Time perspective
Cross-sectional
Enrollment
110 participants (estimated)
Patient registry
No

Groups and cohorts

  • Sedentary adults

    Sedentary adults aged 18-45 years (55 male, 55 female) with bilateral hamstring tightness and no current low back pain, assessed for hamstring tightness (Active Knee Extension test) and lumbar lordosis angle (bubble inclinometer) across three functional sitting postures (upright, slumped, and forward-leaning).

    Other: Hamstring tightness and lumbar lordosis assessment

Interventions

  • OtherHamstring tightness and lumbar lordosis assessment

    Hamstring tightness measured bilaterally with the Active Knee Extension test (digital goniometer) and lumbar lordosis angle (T12-S2) measured with a bubble inclinometer across three functional sitting postures. No therapeutic intervention is administered; these are observational measurements only.

06

What researchers measure

Primary outcomes

  1. Correlation between hamstring tightness and lumbar lordosis angle across three functional sitting postures

    Hamstring tightness is measured as the Active Knee Extension (AKE) deficit in degrees (mean of three trials per limb, using a digital goniometer). The lumbar lordosis angle is measured in degrees using a bubble inclinometer (T12-S2, mean of three trials per posture) in three functional sitting postures: upright, slumped, and forward-leaning. The association between hamstring tightness and the lumbar lordosis angle is assessed for each posture using the Pearson correlation coefficient.

    Time frame: At a single assessment session (cross-sectional; Day 1).

Secondary outcomes

  1. Difference in hamstring tightness between males and females

    Hamstring tightness (bilateral mean Active Knee Extension deficit, in degrees) compared between male and female participants.

    Time frame: At a single assessment session (cross-sectional; Day 1).

  2. Difference in hamstring tightness between the dominant and non-dominant lower limb

    Hamstring tightness (Active Knee Extension deficit, in degrees) compared between the dominant and non-dominant limb. Limb dominance is determined using a three-task behavioral battery.

    Time frame: At a single assessment session (cross-sectional; Day 1).

  3. Difference in lumbar lordosis angle between males and females across the three sitting postures

    Lumbar lordosis angle (degrees, bubble inclinometer, T12-S2) compared between male and female participants in each of the three functional sitting postures (upright, slumped, forward-leaning).

    Time frame: At a single assessment session (cross-sectional; Day 1).

07

Study locations

1 site
08

References and documents

Individual participant data

Plan to share: No

No publications or documents are linked to this record.

09

Timeline

Tracking since Sep 25, 2026
ElapsedEstimatedEstimated, not yet reached

Start is estimated for Aug 2026; primary completion for Oct 2026, 2 months later.

How these figures are worked out, and which studies are left out of them.

Registered
Jun 27, 2026
First posted
Jul 2, 2026
StartEst.
Aug 1, 2026
Primary completionEst.
Oct 1, 2026
CompletionEst.
Dec 1, 2026
Last update
Jul 6, 2026
What these dates mean
Start.
When the first participant enrolled; while estimated, when the study expects to open to recruitment.
Primary completion.
When the last participant was examined or treated to collect data for the study's main question, its primary outcome. A study that stopped early gives the date its data collection stopped.
Completion.
When the last participant's last visit took place, for every outcome, secondary ones and side effects included: the end of the study. Often later than primary completion, sometimes the same day.
Actual and Est.
Actual means the registry says the date has happened. Est. (estimated) is a date the sponsor plans or expects. It can still move, and the sponsor is expected to change it to actual once it has passed.
No changes since tracking began. The registry record was last updated on Jul 6, 2026, before this site started recording changes on Sep 25, 2026. Its history is on ClinicalTrials.gov ↗
10

Registry details

Key details

Study ID
NCT07682142
Lead sponsor
Cairo University
Responsible party
Ahmed youssef saleh saeed (physiotherapist, Nasser Institute For Research and Treatment) — Principal investigator
First posted
Jul 2, 2026
Start date
Aug 1, 2026 (estimated)
Primary completion
Oct 1, 2026 (estimated)
Completion
Dec 1, 2026 (estimated)
Last update
Jul 6, 2026

Study contacts

Ahmed youssef, physiotherapist
Contact
ahmedshamebella@gmail.com
+201008650006

Oversight

FDA-regulated drug
No
FDA-regulated device
No
View the source record on ClinicalTrials.gov ↗

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