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Effect of Hydrotherapy on Children With Brain Tumor

Effect of Hydrotherapy on Performance in Children With Brain Tumor

Status
Completed
Phases
NA
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT07094360
Enrollment
50
Registered
2025-07-30
Start date
2016-11-30
Completion date
2017-04-30
Last updated
2025-07-30

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Pediatric Brain Tumor

Keywords

Hydrotherapy, Performance, Children, Brain tumor

Brief summary

* Background: Brain and spinal cord tumors are the second most common cancers in children (after leukemia). They account for about 1 out of 4 childhood cancers. More than 4,000 central nervous system tumors are diagnosed each year in children and teens. (Blaney et al., 2011). * Aim: It has been reported that those children have easy fatigability so the purpose of this study is to investigate the effectiveness of hydrotherapy on endurance in these Children. * Significance: The effects of physical exercise training interventions for childhood cancer participants are not yet convincing due to small numbers of participants and insufficient study methodology. More and high-quality evidence is needed in order to be able to draft exercise and physical activity guidelines for this population. Despite the positive results of exercise interventions in adult cancer patients, the evidence for benefits in childhood cancer patients is limited (Braam et al., 2013). An 8-week deep water exercise program was clinically effective for improving CRF(Cancer-Related-Fatigue), muscle strength, and several aspects of mood state as compared with usual treatment care at short and medium term in breast cancer survivors reporting a moderate rate of fatigue (Irene et al., 2013). In this study, the investigators are trying to find out the effect of hydrotherapy as a way of fun and amusement that children can do easily with great pleasure and also as a treatment method. * Subjects: Thirty children of both sexes will participate in this study. Inclusion criteria: Children between 5-14 years old after brain tumor resection surgery 2 weeks post-surgery. Exclusion Criteria: Cognitive or mental (developmental), or both, impairment, Children with a genetic disorder, Children with a chronic lung disease, Severe cardiomyopathy (ejection fraction \<40%, ischemia and angina pectoris at rest), Children with a neuromuscular disease. * Methodology: For Evaluation: Lafayette manual muscle tester to assess muscle endurance/strength (Lafayette instrument evaluation, 2015). The pediatric quality of life inventory version 4(PedsQL) is used to assess quality of life (Varni et al., 1999). The nine-minute run-walk test (Guedes et al., 2006) and the timed up-and-down stairs test (Zaino et al., 2004) are to measure Cardiorespiratory fitness. For Treatment: Children will be divided into two groups, control group will receive a land-exercise program and study group will receive the same exercise program then repetition of these exercises under water to study the effectiveness of using hydrotherapy. The program will take 30 minutes (5 minutes each with 1 minute rest in between). The selected program will be in the form of: 1. Sitting while strengthening shoulder horizontal adductors by using weights. 2. Sitting while pushing down by using weights. 3. Sitting while strengthening elbow extensors by using weights. 4. Sitting while holding weights for a while. 5. Standing on uneven surface. 6. Pushing downs by legs. 7. Sitting balance. 8. Sitting with pushing by hands while making legs as glue. 9. Sitting with kicking by legs while fixing hands. 10. Standing and throwing a ball. 11. Weight shifting and recovery while initiating single limb support.

Interventions

Land-based exercise program

OTHERHydrotherapy besides Land-based exercise program

Hydrotherapy besides Land-based exercise program

Sponsors

Cairo University
Lead SponsorOTHER

Study design

Allocation
RANDOMIZED
Intervention model
PARALLEL
Primary purpose
TREATMENT
Masking
NONE

Eligibility

Sex/Gender
ALL
Age
5 Years to 14 Years
Healthy volunteers
No

Inclusion criteria

They will be selected according to the following criteria: 1. Children between 5-14 years old. 2. Children after brain tumor resection surgery 4 weeks post-surgery.

Exclusion criteria

Children who have one or more of the following criteria will be excluded from the study: 1. Children who cannot follow orders or instructions. 2. Children with a genetic disorder. 3. Children with a chronic lung disease. 4. Sever cardiomyopathy (ejection fraction \<40%, ischemia and angina pectoris at rest). 5. Children with a neuromuscular disease.

Design outcomes

Primary

MeasureTime frameDescription
Muscle strength of upper and lower limb muscles4-6 monthsLafayette Manual Muscle Tester: The test was performed by applying force to the limb of a child as he/she resists the force isometrically. The objective of the test is for the clinician to overcome or break the child's resistance. When the resistance break occurs the Lafayette Manual Muscle Tester (MMT) records the peak force and the time required to achieve the break providing reliable, accurate, and stable muscle strength readings that conform to most manual muscle testing protocols. The MMT also features a wide range of customizable options for data storage, preset test times, and force thresholds

Secondary

MeasureTime frameDescription
Pediatric quality of life4-6 monthsThe pediatric quality of life inventory version 4 (PedsQL) is a modular approach to measure health-related quality of life in healthy children and adolescents and those with acute and chronic health conditions. The Pads Measurement Model integrates seamlessly both generic core scales and disease-specific modules into one measurement system. The PedsQL Brain tumor module was used in this study.
Cardiorespiratory fitness4-6 monthsThe Six-minute run-walk test: This test has been used as an adaptation of the 12-minute Cooper test for children under the age of 12, and is also used in Brazil and internationally as an alternative to motor test batteries for CRF assessment (Gaya et al., 2007). Currently, it becomes modified to the 6-minute walk

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 4, 2026