NCT06529874Recruiting
Pressure Pain Tolerance in Relation to Balance and Strength in Children
Pressure Pain Tolerance in Relation to Balance and Strength in Children With Sickle Cell Anemia
Source: ClinicalTrials.gov · Last updated 1 Apr 2025 · Not updated for over 12 months - ask the site whether it is still open
Brief summary (registry, in English)
Sickle cell disease (SCD) is the most frequent life-threatening genetic hemoglobinopathy in the world and occurs due to the synthesis of abnormal hemoglobin S (HbS).Cells with sickle cell hemoglobin are stiff and sticky. When they lose their oxygen, they form into the shape of a sickle or crescent. This can cause pain and tissue damage. Significant decrease in exercise capacity was seen in sickle cell anemic children. In the absence of a guidelines that can guide the prescription of exercise in SCD children. This study is a step for determine the forms of prescription of pain on the balance and muscle strength to build up in future studies a safety of physical exercises for children with sickle cell anemia and improve their functional abilities.
- Status (registry)
- Recruiting
- Study type
- Interventional
- Enrollment
- 80 (estimated)
- First submitted
- 25 Jul 2024
- Start date
- 1 Feb 2024
- Primary completion date
- 1 Aug 2025
- Lead sponsor
- Adly A Adam
- Diseases
- Sickle cell disease
- NCT number
- NCT06529874
What you commit to
- Study type: Interventional
- Planned participants: 80
- From 1 Feb 2024 to the primary completion date, 1 Aug 2025
- 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.
Prior treatment
- Recent thoracoabdominal surgery.
Other illness
- Defined cardiovascular or respiratory disorders.
- Renal failure.
- Myocardial infarction, mainly within last month.
- Unstable angina.
Other
- Thoracic or abdominal aneurysm or current pneumothorax.
- Painful vaso-occlusive crises.
- Muscular contractures, Joints' stiffness, or deformities.
- Neuromuscular problems i.e., myositis or peripheral neuropathy.
Who the study is looking for
- Age range range was 9-14 years old.
- Could follow given instructions.
- Children with Sickle cell anemia were medically stable, and take their medications regularly.
- Children with Sickle cell anemia had experience of chronic pain that lasts more than 6 months.
- All children with Sickle cell anemia have average weight, height, and body mass index based on their age percentiles.
- All normal healthy children did not participating in regular sport activities, particularly including lower limb strengthening.
Age in the registry: 9 years to 14 years · Sex: All · Accepts healthy volunteers
Sites (1)
Sites in registry order. Pick your city on the disease page to sort them by distance.
| Site | City | Country | Site status |
|---|---|---|---|
| El-Tahrir st.- in front of Ben El-Sarayat, Ad Doqi Al Giza, Giza Governate Coordinator of this site? Confirm its status | Giza | Egypt | Recruiting |
This page is information, not medical advice. Discuss any trial with your doctor.