ClinicalTrials.gg
RecruitingNCT06867003Updated Jul 9, 2025

Comparison of Exercise With & Without Bracing in Office Workers With Kyphosis

An interventional study of physical therapy with bracing and physical therapy without bracing in Kyphosis, sponsored by Riphah International University. Recruiting at 1 site in Pakistan. Open to participants aged 30 Years to 45 Years. Per ClinicalTrials.gov, last updated 2025-07-09.

Sponsored by Riphah International University · Not applicable, Interventional, and Health services research

From the registry’s dates

  • Primary completion was expected by Feb 2026, 8 months ago, but the record still lists the study as recruiting.
  • Started Feb 2025; still recruiting 1 year 8 months later.
Phase
Not applicable
Study type
Interventional
Enrollment
36
Allocation
Randomized
Ages
30 Years to 45 Years
Sex
All
01

Study summary

The study aims to Compare PT and bracing in improving posture, pain, and functionality in patient with kyphosis.

It also assess the additive benefits of combining PT with bracing. It also identify sustainable, non-surgical approaches for managing kyphosis in office

Read the detailed description

The study focuses on understanding Kyphosis, defined as excessive forward curvature of the thoracic spine, has become increasingly prevalent in modern work environments due to the sedentary nature of desk jobs. Kyphosis, characterized by a rounded upper back or "hunchback" appearance, is a clinical and postural problem with significant physical, functional, and psychosocial implications. Among office workers, the condition is primarily postural, driven by long hours of desk work, inappropriate ergonomic settings, and inadequate postural awareness. The increasing prevalence of kyphosis in this demographic has led to a pressing need for effective nonsurgical management strategies, including physical therapy (PT) and spinal bracing.

02

Conditions studied

  • Kyphosis

Browse trials for

Keywords

  • Kyphosis
03

In context

Kyphosis

132 studies on the registry are indexed under Kyphosis; 31 are open to participants now.

This study's planned enrollment of 36 is below the median of 44 across 82 interventional studies indexed under Kyphosis.

Browse Kyphosis studies →

Lead sponsor

Riphah International University is the lead sponsor of 2,193 studies on the registry; 650 are open to participants now.

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

04

Who can participate

Ages eligible
30 Years to 45 Years
Sexes eligible
All
Accepts healthy volunteers
No

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

  • Office workers diagnosed with Postural Kyphosis
  • age limit 30 to 45years
  • Experience of upper back or neck pain lasting at least three months
  • Spend a minimum of 6 hours per day in a seated position for work.

Exclusion criteria

Exclusion Criteria:

  • History of spinal surgery, severe scoliosis, or other significant spinal deformities.

Current engagement in any structured physical therapy program or use of bracing for posture. Any neurological or musculoskeletal disorders impacting posture or movement.

05

Study design

Phase
Not applicable
Primary purpose
Health services research
Allocation
Randomized
Intervention model
Parallel assignment
Masking
Single (Participant)
Enrollment
36 participants (estimated)

Study arms

  • Experimental
    Physical therapy with bracing

    Effectiveness of physical therapy with bracing

    Other: physical therapy with bracing

  • Placebo comparator
    physical therapy without bracing

    Effectiveness of physical therapy without bracing

    Other: physical therapy without bracing

Interventions

  • Otherphysical therapy with bracing

    Strengthens the upper back muscles and reduces tension: 1. Stand or sit with an upright posture and shoulders pulled back 2. Squeeze your shoulder blades together as tightly as you can and hold for five to ten seconds

    Also known as: Exercise

  • Otherphysical therapy without bracing

    Strengthens the upper back muscles and reduces tension: 1. Stand or sit with an upright posture and shoulders pulled back 2. Squeeze your shoulder blades together as tightly as you can and hold for five to ten seconds

06

What researchers measure

Primary outcomes

  1. Oswestry Disability Index (ODI)

    The questionnaire consists of 10 sections, each with 6 response options (scored 0 to 5). If all 10 sections are completed, the maximum score is 50.

    Time frame: 4 weeks

  2. Visual Analogue Scale (VAS)

    A 10 cm horizontal line with "No Pain" (0) on the left and "Worst Pain" (10) on the right.

    Time frame: 4 weeks

07

Study locations

1 of 1 sites recruiting
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 reachedSimilar studies: half by the dot; the band is the middle halfHalf of similar studies reached it by the dot; the band is the middle half, from a quarter to three quarters

Started Feb 2025 (actual). Primary completion is estimated for Feb 2026, 12 months after the start.

Of 56 non-industry interventional studies with no phase under Kyphosis, half reached primary completion within 9 months of starting (the median), counting those still running; a quarter within 4 and three quarters within 30. This study's planned 12 months is above that.

Counting every sponsor, half of 58 studies reached it within 9 months; a quarter within 4 and three quarters within 30.

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

Registered
Mar 4, 2025
First posted
Mar 10, 2025
StartActual
Feb 20, 2025
Primary completionEst.
Feb 20, 2026
CompletionEst.
Feb 20, 2026
Last update
Jul 9, 2025
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 9, 2025, before this site started recording changes on Sep 25, 2026. Its history is on ClinicalTrials.gov ↗
10

Registry details

Key details

Study ID
NCT06867003
Responsible party
Sponsor
First posted
Mar 10, 2025
Start date
Feb 20, 2025
Primary completion
Feb 20, 2026 (estimated)
Completion
Feb 20, 2026 (estimated)
Last update
Jul 9, 2025

Study contacts

Ataur Rahman
Contact
ataur.rahman@riphah.edu.pk
03038371112
Ataur Rahman, MS-PT
principal investigator · Riphah International University

Oversight

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

Interested in this study?

Eligibility is decided by the study team. Share this record with your doctor or contact the team directly.

Contact study team

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