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NCT07882069Completed

Effect of ACTIVE-Care on Cancer-Related Fatigue, Hope, and Psychological Resilience in Adolescents With Acute Lymphoblastic Leukemia

Effect of the ACTIVE-Care Integrated Physical Activity-Based Supportive Care Program on Cancer-Related Fatigue, Hope, and Psychological Resilience in Adolescents With Acute Lymphoblastic Leukemia: A Randomized Controlled Trial

Source: ClinicalTrials.gov · Last updated 20 Oct 2026

Brief summary (registry, in English)

This study aimed to evaluate the effects of the ACTIVE-Care Integrated Physical Activity-Based Supportive Care Program on cancer-related fatigue, hope, and psychological resilience in adolescents with acute lymphoblastic leukemia (ALL). Seventy adolescents aged 13-16 years participated in a parallel-group randomized controlled trial. The intervention group received a six-week program integrating individualized physical activity with psychosocial support, while the control group received usual care. Outcomes were assessed at baseline and immediately after the six-week intervention.

Status (registry)
Completed
Study type
Interventional
Enrollment
70 (actual)
First submitted
11 Oct 2026
Start date
1 Jul 2026
Primary completion date
7 Jul 2026
Lead sponsor
Selcuk University
NCT number
NCT07882069

What you commit to

  • Study type: Interventional
  • Participants enrolled: 70
  • From 1 Jul 2026 to the primary completion date, 7 Jul 2026
  • 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

  • Receiving intensive treatment for active relapse, being clinically unstable, or not being medically cleared by the responsible pediatric hematology-oncology specialist to participate in physical activity;

Other illness

  • Having a severe cardiovascular, respiratory, neurological, or musculoskeletal condition that contraindicated participation in exercise;
  • Being unable to participate in the intervention or data collection procedures because of a diagnosed severe psychiatric or cognitive disorder; or

Other

  • Having a severe functional limitation that prevented the safe performance of physical activity;
  • Participating in another structured exercise or psychosocial intervention program during the study period that could affect the study outcomes.

Who the study is looking for

  • Aged 13-16 years;
  • Diagnosed with acute lymphoblastic leukemia (ALL) by a pediatric hematology-oncology specialist;
  • Undergoing consolidation or maintenance chemotherapy;
  • Clinically stable and medically cleared by the responsible pediatric hematology-oncology specialist to participate in moderate-intensity physical activity;
  • Able to read and understand Turkish and have sufficient cognitive capacity to complete the data collection forms independently or, when necessary, with assistance from the researcher; and
  • Willing to participate in the study, with written assent obtained from the adolescent and written informed consent obtained from a parent/legal guardian.

Age in the registry: 13 years to 18 years · Sex: All · Does not accept healthy volunteers

Full criteria on ClinicalTrials.gov

Sites (1)

Sites in registry order. Pick your city on the disease page to sort them by distance.

SiteCityCountrySite status
Selçuk University
Coordinator of this site? Confirm its status
KonyaTurkey (Türkiye)Unknown status

This page is information, not medical advice. Discuss any trial with your doctor.