NCT07328165

Brief Summary

Children with Down syndrome often exhibit diminished physical fitness levels and lower bone mass. Numerous factors contribute to this decrease in bone mass density, including decreased levels of leptin, reduced muscle mass and strength, impaired balance, and skeletal abnormalities. These factors further exacerbate the risk of developing osteoporosis in this population. Therefore, it is crucial to prioritize interventions that focus on maximizing peak bone mass during childhood in order to enhance the quality of life for adults with Down syndrome. The study aims to compare the impact of core stability exercises and respiratory muscle strengthening exercises on bone mineral density in children with Down syndrome. Sixty Children with Down syndrome will be assessed and included in this study. The age of children will range from 10 to 13 years. Children will be allocated randomly into three groups (control and two study group A \& B). The control group receives a physical therapy program, study group A receives traditional physical therapy program with core stability exercises, and study group B receives traditional physical therapy program with respiratory muscle strengthening exercises. Groups will be evaluated using dual energy X-ray absorptiometry DXA (DPX-IQ, version 4.6A). Bone mineral density (BMD) of femoral neck and lumbar spine will be determined and the mean density will be expressed as g/cm2.

Trial Health

65
Monitor

Trial Health Score

Automated assessment based on enrollment pace, timeline, and geographic reach

Enrollment
60

participants targeted

Target at P25-P50 for not_applicable

Timeline
0mo left

Started Feb 2026

Shorter than P25 for not_applicable

Status
not yet recruiting

Health score is calculated from publicly available data and should be used for screening purposes only.

Trial Relationships

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Study Timeline

Key milestones and dates

Study Progress76%
Feb 2026Jun 2026

First Submitted

Initial submission to the registry

December 26, 2025

Completed
14 days until next milestone

First Posted

Study publicly available on registry

January 9, 2026

Completed
1 month until next milestone

Study Start

First participant enrolled

February 20, 2026

Completed
2 months until next milestone

Primary Completion

Last participant's last visit for primary outcome

May 1, 2026

Completed
1 month until next milestone

Study Completion

Last participant's last visit for all outcomes

June 1, 2026

Expected
Last Updated

February 3, 2026

Status Verified

December 1, 2025

Enrollment Period

2 months

First QC Date

December 26, 2025

Last Update Submit

February 2, 2026

Conditions

Outcome Measures

Primary Outcomes (1)

  • Bone mineral density (BMD) of femoral neck and lumbar spine

    . Groups will be evaluated using dual energy X-ray absorptiometry DXA (DPX-IQ, version 4.6A).

    8 weeks

Study Arms (3)

Core Stability Exercise Group

EXPERIMENTAL

This group will receive core stability exercises in addition to physical therapy program as control group.

Behavioral: Core Stability Exercise Group

Respiratory Muscle Strengthening Group

EXPERIMENTAL

This group will receive respiratory muscle strengthening exercises in addition to physical therapy program as control group

Device: Respiratory Muscle Strengthening Group

Control Group

ACTIVE COMPARATOR

The control group will receive the physical therapy program and conduct three times peer week over 8 consecutive weeks under the supervision of a physical rehabilitation specialist

Behavioral: Control /Conventional Physiotherapy Group

Interventions

Based on Jeffrey's protocol, the protocol includes specific spinal stabilization exercises, lumbar-pelvic proprioception retraining, and abdominal maneuvers (holding the abdomen in) and multifidus muscle contraction, followed by maintaining stabilization maneuver using dynamic stability achieved in different positions (supine, prone, and squatting) and addition of dynamic elements (limb movement, use of Swiss ball) in later stages.

Core Stability Exercise Group

By using a threshold inspiratory muscle training (IMT) (Respironics, Cedar Grove, NJ, USA). Frequency 3 time per week for 8 weeks. It is a spring-loaded valve that inspiratory resistance can be adjusted. This training last for 30 min. To develop muscle strength; during the first 10 min of practice, threshold IMT will be used in 10 series of 60s each, separated by rest periods of 60s. To develop endurance; during the final 20 min, the equipment will be used uninterruptedly. Prior to the beginning of each session, the pressure threshold load throughout the practice will be 50 % of Maximum Inspiratory pressure that will be calculated during the evaluation of children.

Respiratory Muscle Strengthening Group

The primary focus of the program was to improve bone mineral density. Each session will be conducted 60 minutes and consist of weight bearing exercises and strengthen exercises in the form of isometric exercises;

Control Group

Eligibility Criteria

Age10 Years - 13 Years
Sexall
Healthy VolunteersNo
Age GroupsChild (0-17)

You may qualify if:

  • Age will range from 10-13 years
  • Diagnosed with Down syndrome.
  • Children with the ability to understand and follow verbal commands and instructions used during training and tests
  • Able to stand and walk independently

You may not qualify if:

  • Any neurological, mobility disorders, vision or hearing loss, cardiac anomalies or musculoskeletal disorder
  • With asthma or any chronic chest diseases
  • With significant tightness or deformities in the lower limbs and limber spine

Contact the study team to confirm eligibility.

Sponsors & Collaborators

MeSH Terms

Conditions

Down SyndromeBone Diseases, Metabolic

Condition Hierarchy (Ancestors)

Intellectual DisabilityNeurobehavioral ManifestationsNeurologic ManifestationsNervous System DiseasesAbnormalities, MultipleCongenital AbnormalitiesCongenital, Hereditary, and Neonatal Diseases and AbnormalitiesChromosome DisordersGenetic Diseases, InbornBone DiseasesMusculoskeletal DiseasesMetabolic DiseasesNutritional and Metabolic Diseases

Study Design

Study Type
interventional
Phase
not applicable
Allocation
RANDOMIZED
Masking
NONE
Purpose
TREATMENT
Intervention Model
PARALLEL
Sponsor Type
OTHER
Responsible Party
PRINCIPAL INVESTIGATOR
PI Title
Principal Investigator

Study Record Dates

First Submitted

December 26, 2025

First Posted

January 9, 2026

Study Start

February 20, 2026

Primary Completion

May 1, 2026

Study Completion (Estimated)

June 1, 2026

Last Updated

February 3, 2026

Record last verified: 2025-12