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NCT07875894Not yet recruiting

Effects of Sensorimotor Balance Training vs Digitally Augmented Core Stabilization in Women With Osteoporosis

Effects of Sensorimotor-Based Balance Training Versus Digitally Augmented Core Stabilization on Postural Control and Fall Risk in Postmenopausal Women With Osteoporosis

Source: ClinicalTrials.gov · Last updated 15 Oct 2026

Brief summary (registry, in English)

This randomized controlled trial aims to compare the effects of sensorimotor-based balance training and digitally augmented core stabilization on postural control and fall risk in postmenopausal women with osteoporosis. Osteoporosis is a common condition in postmenopausal women that can impair balance, reduce functional mobility, and increase the risk of falls and fractures. Eligible participants will be randomly assigned to one of two intervention groups. Group A will receive a structured sensorimotor-based balance training program, while Group B will receive a digitally augmented core stabilization exercise program supported through the HEP2Go platform and monitored via WhatsApp. Both groups will receive supervised physiotherapy sessions three times per week for 8 weeks. Outcome measures including postural control, fall risk, spinal alignment, core muscle endurance, proprioception, muscle strength, adherence, and usability will be assessed before and after the intervention. The findings of this study may provide evidence regarding effective physiotherapy strategies for improving balance and reducing fall risk in postmenopausal women with osteoporosis.

Status (registry)
Not yet recruiting
Study type
Interventional
Enrollment
40 (estimated)
First submitted
16 Sept 2026
Start date
1 Sept 2026
Primary completion date
30 Jun 2027
Lead sponsor
Riphah International University
Diseases
Osteoporosis
NCT number
NCT07875894

What you commit to

  • Study type: Interventional
  • Planned participants: 40
  • From 1 Sept 2026 to the primary completion date, 30 Jun 2027
  • 1 site in 1 country
  • Visits and tests: ask the trial team, the registry does not list them

Built from the registry fields of ClinicalTrials.gov. It describes the study, not your situation.

Who cannot take part

Copied verbatim from ClinicalTrials.gov and grouped by topic. Only the trial team decides who can take part.

Other illness

  • • Women with severe mobility impairments.
    • History of fragility fracture within the last 6 months
    • Women with cognitive conditions affecting participation.
    • Women with lower limb joint injury or surgery.

Who the study is looking for

  • PMW diagnosed with osteoporosis through DEXA (T-score ≤ -2.5)
  • Age (45-70 years).
  • Able to participate in sessions and walk independently.
  • Mild to moderate Balance impairment as per BBS

Age in the registry: 45 years to 70 years · Sex: Female · Does not accept healthy volunteers

Full criteria on ClinicalTrials.gov

Sites (1)

Sites in registry order. Pick your city on the disease page to sort them by distance.

SiteCityCountrySite status
Muhammad Adnan Saeed
Coordinator of this site? Confirm its status
IslamabadPakistanUnknown status

This page is information, not medical advice. Discuss any trial with your doctor.