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Acute Lymphoblastic LeukemiaNCT06794762

Effects of Core Stabilization Exercises in Children With Acute Lymphoblastic Leukemia

A study testing Conventional exercises and Core stabilization exercises in addition to conventional exercises in people with Acute Lymphoblastic Leukemia, run by Karamanoğlu Mehmetbey University at 1 site in Turkey (Türkiye).

Completed

Finished. The study has ended and is not enrolling. Results may be posted on the official record.

Official record
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Trial summary

The goal of this clinical trial is to investigate the effects of core stabilization exercises applied in addition to the conventional exercise program on physical function, functional muscle strength, functional exercise capacity, postural control and fatigue in children with acute lymphoblastic leukemia receiving… Read more about this study

Who is it for?
Ages 5 to 18 years
Conditions the study is for
Acute Lymphoblastic Leukemia
What is being tested?
Conventional exercises and Core stabilization exercises in addition to conventional exercises
Could I receive a placebo?
No, everyone receives an active treatment
How many people
27 participants
Where
1 siteTurkey (Türkiye)
Study dates
14 Jan 2025to 15 Mar 2026
Phase
Interventional
Are there results?
None posted in the registry

Key requirements

Who can take part, as listed by the sponsor. Only the study team can confirm whether you are eligible, so take this list to your doctor.

  • Ages 5 to 18 years
  • All sexes
  • No healthy volunteers
  • Child, Adult

Who may be able to join

  • Children aged 5-18
  • Diagnosed with ALL
  • In the maintenance phase of chemotherapy
  • Children without acute thrombosis, active ischemia, hemodynamic instability
  • Children without uncontrolled pain
  • Children who can follow verbal instructions.

Who cannot join

  • Children who have received or are receiving cranial radiotherapy
  • Children with any cardiovascular disease, acute or chronic respiratory disease
  • Children with acute or chronic bone, joint, muscle problems
  • Children diagnosed with neuromotor deficits or genetic disorders
  • Children with vision problems other than refractive errors

Trial locations and contacts

1 site in 1 country.

Turkey (Türkiye)1 site
  • Necmettin Erbakan University

    Konya, 42090

Other trials in Turkey (Türkiye)

About this study

Official title: Examination of the Effects of Core Stabilization Exercises on Physical Function, Functional Muscle Strength, Functional Exercise Capacity, Postural Control and Fatigue in Children With Acute Lymphoblastic Leukemia Receiving Maintenance Treatment

The goal of this clinical trial is to investigate the effects of core stabilization exercises applied in addition to the conventional exercise program on physical function, functional muscle strength, functional exercise capacity, postural control and fatigue in children with acute lymphoblastic leukemia receiving maintenance treatment.

Participants will be divided into two groups; the first group will be given a conventional exercise program, while the second group will be given core stabilization exercises in addition to the conventional exercise program.

Read the detailed description

Acute Lymphoblastic Leukemia (ALL) is a malignancy resulting from the abnormal proliferation of lymphoid cells that can invade the bone marrow, blood, and extramedullary regions, and it is the most common malignancy in childhood. Specific chemotherapy-related problems are frequently observed in children with ALL. These include a reduction in cardiopulmonary fitness, balance, posture, proximal muscle strength, and flexibility, as well as postural control issues and functional mobility impairments, in addition to fatigue.

The aim of this study is to investigate the effects of core stabilization exercises, applied in addition to a conventional exercise program, on physical function, functional muscle strength, functional exercise capacity, postural control, and fatigue in children with Acute Lymphoblastic Leukemia undergoing maintenance therapy.

Participants will be divided into two groups: the first group will follow a conventional exercise program, while the second group will receive core stabilization exercises in addition to the conventional program. All participants will be randomly assigned to the groups using the software available at http://www.randomizer.org. The exercise sessions will be conducted three times a week for a total of 8 weeks, with 24 sessions in total. Demographic information will be recorded for participants who agree to take part in the study and meet the inclusion criteria. The scales and tests designed to assess the participants' physical function, functional muscle strength, functional exercise capacity, postural control, and fatigue will be administered both before and after the study.

Being tested
Conventional exercises, Core stabilization exercises in addition to conventional exercises
Keywords
Acute Lymphoblastic Leukemia, Maintenance Chemotherapy, Rehabilitation, Exercise, Core Stabilization Exercises, Cancer, Physical Function, Functional Muscle Strength, Functional Exercise Capacity, Postural Control, Fatigue
Medical subject headings
Precursor Cell Lymphoblastic Leukemia-Lymphoma, Motor Activity, Neoplasms, Fatigue

What participants receive

What participants receive. In a randomised study each person is assigned to one group by chance.

  • Conventional exercisesOther

    Aerobic exercise and stretching exercises will be applied in the conventional exercise program.

    A 20-30 minute walking will be done as aerobic exercise. Stretching exercises will be done for major muscle groups in 3 sets and 10 repetitions.

  • Core stabilization exercises in addition to conventional exercisesOther

    In addition to the conventional exercise program, core stabilization exercises will be applied. During the exercises, participants will be trained on neutralizing the spine and working the transverse abdominis and multifidus muscles, correct postural control, and performing the exercises with diaphragmatic breathing.

Study groups in NCT06794762
Study groupRoleWhat they receive
Control groupExperimentalExercises will be applied to the participants participating in the study 3 days a week, 8 weeks, and 24 sessions in total.
Receives: Other: Conventional exercises
Intervention groupExperimentalExercises will be applied to the individuals participating in the study 3 days a week, 8 weeks, and 24 sessions in total. Exercises will be applied after the conventional therapy sessions.
Receives: Other: Core stabilization exercises in addition to conventional exercises

What is being measured

The primary outcome is the main question the study is designed to answer.

  1. Timed Up and Go Test (TUG)

    This test aims to evaluate the physical function.

    Measured: Before 8 weeks of treatment

  2. Timed Up and Go Test (TUG)

    This test aims to evaluate the physical function.

    Measured: After 8 weeks of treatment

  3. Sit-up Test

    This test aims to evaluate the functional muscle strength

    Measured: Before 8 weeks of treatment

  4. Sit-up Test

    This aims to evaluate the functional muscle strength.

    Measured: After 8 weeks of treatment

  5. 6-Minute Walk Test

    This test aims to evaluate the functional exercise capacity.

    Measured: Before 8 weeks of treatment

  6. 6-Minute Walk Test

    This test aims to evaluate the functional exercise capacity.

    Measured: After 8 weeks of treatment

  7. Balance Error Scoring System

    This test aims to evaluate the postural control.

    Measured: Before 8 weeks of treatment

  8. Balance Error Scoring System

    This test aims to evaluate the postural control.

    Measured: After 8 weeks of treatment

  9. Pediatric Quality of Life Multidimensional Fatigue Scale

    This scale aims to evaluate the fatigue in pediatric patients.

    Measured: Before 8 weeks of treatment

  10. Pediatric Quality of Life Multidimensional Fatigue Scale

    This scale aims to evaluate the fatigue in pediatric patients.

    Measured: After 8 weeks of treatment

Timeline

From the start of the study to its completion; the mark is today. Estimated dates are the sponsor’s plan.

  1. First posted27 Jan 2025
  2. Study start14 Jan 2025
  3. Primary completion15 Mar 2026
  4. Study completion15 Mar 2026

Resources

More details

For doctors and researchers: how the study is designed, who runs it, and its registry IDs.

Study design
Study type
Interventional
Phase
Phase N/A
Primary purpose
Treatment
Allocation
Randomised
Intervention model
Parallel groups
Masking
Single blind
Who is masked
Participant
Enrolment
27 participants (actual)
IDs, dates and publications
ClinicalTrials.gov ID
NCT06794762
Sponsor's protocol ID
2024/023-12
Status last verified
Oct 2026
First submitted
13 Jan 2025
Last updated
7 Oct 2026
Results posted
No
FDA-regulated drug
No
FDA-regulated device
No
Individual data sharing
No

Questions about this trial

What is this clinical trial studying?

A study testing Conventional exercises and Core stabilization exercises in addition to conventional exercises in people with Acute Lymphoblastic Leukemia, run by Karamanoğlu Mehmetbey University at 1 site in Turkey (Türkiye).

The full registered description is in the About this study section and the official record.

Who may be eligible to take part?

The sponsor lists 6 inclusion and 5 exclusion criteria. Eligibility is decided by the study team after screening, so read the full criteria and contact a listed site.

Is this clinical trial currently recruiting?

The record says: finished, as of the sponsor's last update on 7 Oct 2026. Status can change between updates, so confirm with the study contact before making plans.

Where is the study taking place?

The record lists 1 site in Turkey (Türkiye). Whether a site is taking part right now should be confirmed with that site. See every site.

What are the possible benefits and risks?

They depend on the study and the treatment, and no study can promise a benefit. The study team explains the known risks during informed consent, before anyone joins; the record itself does not list them.

Are results available for this study?

The study is completed, but results are not available in the source record. That does not mean the treatment did or did not work.

How can a doctor refer a patient or contact the research team?

The record lists no contact. The official record names the sponsor, who can be asked directly. AzTrials does not enrol participants or take referrals.

What does the primary outcome measure?

Timed Up and Go Test (TUG) (time frame: Before 8 weeks of treatment). The study lists 10 primary outcomes in all. It is what the study was designed to measure, not a finding.

Where can I read the original study information?
Does a listing mean the treatment is approved or proven to work?

No. A listing means the study is registered. It does not show that the treatment is safe, works, or is approved by a regulator.

How often is this information updated?

AzTrials copies changed records from ClinicalTrials.gov every night and reloads the whole registry every week. The sponsor last updated this record on 7 Oct 2026.

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