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Active Not RecruitingNCT07068360

Development and Validation of MPF to Prevent and Mitigate Postural Hyperkyphosis in Postmenopausal Women

Development and Validation of a Multimodal Physiotherapy Framework to Prevent and Mitigate Postural Hyperkyphosis in Postmenopausal Women: A Randomized Controlled Trial

Status
Active Not Recruiting
Phase
N/A
Study type
Interventional
Enrollment
72 (actual)
Sponsor
Superior University · Academic / Other
Sex
Female
Age
35 Years – 70 Years
Healthy volunteers
Not accepted

Summary

Postural hyperkyphosis is common in postmenopausal women and leads to spinal dysfunction, pain, impaired balance, and increased fall risk. This study aims to develop and validate a multimodal physiotherapy framework to prevent and manage hyperkyphosis in this population. A randomized controlled trial will be conducted at Allied Hospital with 72 postmenopausal women aged 40-75 years, divided into intervention (multimodal physiotherapy with conventional care) and control (conventional care only) groups.

Detailed description

The intervention includes strength, flexibility, postural correction, and balance training. The primary outcome is the change in Cobb's angle measured via radiographs; secondary outcomes include functional mobility and balance assessments using the Timed Up and Go Test, Berg Balance Scale, and Functional Reach Test. Data will be analyzed using SPSS v26. The study is expected to show significant improvements in spinal alignment, strength, balance, and reduced fall risk. The framework may offer a cost-effective, evidence-based approach for clinical and community rehabilitation

Conditions

Interventions

TypeNameDescription
COMBINATION_PRODUCTStrength Training +Postural Correction Exercises + Balance Training +Flexibility ExercisesInterventions details (Group A) Strength Training Postural Correction Exercises Balance Training Exercises Flexibility Exercises:
DIAGNOSTIC_TESTStandard Intervention (Control Group)The control group will receive standard physiotherapy for postural hyperkyphosis. The standard intervention will consist of: Postural education: Educating participants on proper posture, body mechanics, and ergonomics in daily activities. Basic stretching exercises targeting the thoracic spine and back muscles. Recommendations for low-impact aerobics activities (e.g., walking or cycling) to promote overall healthThe standard intervention will be delivered over the same 12-week period, with two sessions per week. This group will not receive the integrated multimodal framework with strength training, postural correction, balance training, and flexibility exercises that the experimental group receives. Duration and Frequency

Timeline

Start date
2025-04-17
Primary completion
2025-12-01
Completion
2026-06-01
First posted
2025-07-16
Last updated
2025-07-16

Locations

1 site across 1 country: Pakistan

Source: ClinicalTrials.gov record NCT07068360. Inclusion in this directory is not an endorsement.