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"Exercise Intervention to Increase Physical Activity in Young Sarcoma Survivors (Sport Ist Herzenssache)"

Effects of an Individualized, Smartwatch-Supported Exercise Intervention on Physical Activity, Cardiorespiratory Fitness, Limb Function and Quality of Life in Adolescent and Young Adult Survivors of Bone and Soft Tissue Sarcoma: A Randomized Controlled Trial (Sport Ist Herzenssache)

Status
Not yet recruiting
Phases
Unknown
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT07729059
Enrollment
46
Registered
2026-07-27
Start date
2026-08-01
Completion date
2028-07-31
Last updated
2026-07-27

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

Conditions

Bone Sarcoma, Soft Tissue Sarcoma (STS)

Keywords

Exercise, Physical Activity, Soft Tissue Sarcoma, Bone Sarcoma, Cancer Survivorship, Adolescents and Young Adults, Cardiorespiratory Fitness, Quality of Life, Limb Function

Brief summary

Survivors of bone and soft tissue sarcoma often face long-term health problems after their cancer treatment, such as muscle weakness, joint stiffness, and reduced heart and lung fitness. Because of this, many survivors are less physically active than their healthy peers, which can further increase their risk of heart disease and other late effects later in life. This study, called "Sport ist Herzenssache" ("Sports is a Matter of the Heart"), tests whether a personalized exercise program can help young survivors (aged 15-39) become more physically active. All participants receive a fitness tracker (smartwatch) to monitor their daily activity. Half of the participants are randomly assigned to also receive an individualized home exercise plan, including strength and endurance training, with some sessions guided online by an exercise specialist. Before and after an 8-week exercise period (with continuous activity tracking for about 13 weeks total), participants complete simple physical tests (such as walking and balance tests), a heart and fitness check-up, and questionnaires about their quality of life and energy levels. The main goal is to find out whether the personalized exercise plan helps participants become more active in daily life, measured in minutes of moderate-to-intense activity per day. The study also looks at effects on heart health, physical function, and overall well-being. The results will help determine whether structured exercise support should become a standard part of long-term follow-up care for young sarcoma survivors.

Detailed description

Survivors of pediatric and adolescent bone and soft tissue sarcomas frequently experience long-term sequelae including reduced muscle strength, impaired joint mobility, and diminished cardiorespiratory fitness, often resulting from multimodal oncological therapy (surgery, chemotherapy, radiotherapy). These sequelae contribute to persistently low levels of physical activity compared to healthy peers, which in turn is associated with an elevated risk of cardiovascular disease-a risk already increased 2- to 10-fold in this population due to cardiotoxic treatment exposure (e.g., anthracyclines, thoracic irradiation). Despite established benefits of physical activity in reducing fatigue, improving quality of life, and lowering cardiovascular morbidity, structured exercise programs are not yet routinely integrated into long-term follow-up care for sarcoma survivors. This monocentric, randomized controlled trial ("Sport ist Herzenssache") aims to evaluate the effectiveness of an individualized, partially supervised, digitally supported exercise intervention in increasing moderate-to-vigorous physical activity (MVPA) among adolescent and young adult (AYA) survivors of bone and soft tissue sarcoma during routine oncological follow-up care. Eligible participants are aged 15-39 years, have completed local tumor therapy (surgery and/or radiotherapy) more than 12 months prior to enrollment, and are receiving follow-up care at the Sarcoma Center of the University Hospital Essen. Following informed consent, participants will be randomized 1:1, stratified by tumor location (lower extremity/pelvis, thorax, other), into two groups: (1) a control group receiving a wearable activity tracker (Garmin Venu® Sq 2) for self-monitoring, and (2) an intervention group receiving the same wearable device plus an individualized, partially supervised home-based exercise program over 8 weeks, combining endurance/cardio training (60 min/week) and strength/aerobic sessions (3 × 30 min/week), in accordance with WHO physical activity recommendations and exercise guidelines for cancer survivors. Supervised sessions are delivered via video conferencing by trained exercise therapists. Physical activity is monitored continuously via wearable device across a total observation period of approximately 13-15 weeks in both groups. At baseline and after the observation period, participants undergo a comprehensive assessment including functional mobility testing (Timed Up and Down Stairs, Timed Up and Go, 6-Minute Walk Test, modified Clinical Test of Sensory Interaction in Balance), goniometry, handheld dynamometry, and cardiopulmonary evaluation (spiroergometry, echocardiography, 12-lead ECG). Patient-reported outcomes include health-related quality of life, cancer-related fatigue, physical functioning, and self-rated health status. The primary endpoint is average daily MVPA (minutes/day), measured objectively via wearable device. Secondary endpoints include cardiorespiratory fitness (VO2max), cardiovascular risk factors, orthopedic function, and patient-reported quality of life and fatigue. Exploratory analyses will examine correlations between MVPA and physical/psychosocial outcomes, as well as associations with physical activity levels during acute cancer therapy. Based on a two-sided t-test with α = 0.05 and 80% power, a total sample size of n = 42 (21 per arm) is required to detect a clinically meaningful increase in MVPA from an expected baseline of 40 min/day (SD = 20) toward the WHO-recommended target of 60 min/day. Accounting for an estimated 10% dropout rate, recruitment aims to enroll 46 participants over a two-year period. This study addresses a critical gap in survivorship care by generating evidence on the feasibility and efficacy of a structured, individualized exercise intervention to promote long-term physical activity, cardiovascular health, and quality of life in young sarcoma survivors, with the goal of informing the integration of exercise therapy as a standard component of long-term oncological follow-up care.

Interventions

An 8-week individualized, partially supervised home-based exercise program designed to increase physical activity in accordance with exercise guidelines for cancer survivors. The program is tailored to each participant's functional status, based on a comprehensive baseline assessment (functional testing, cardiopulmonary evaluation, and a structured counseling session addressing individual interests, concerns, and goals). The program consists of: Endurance training: 60 minutes/week (e.g., walking, cycling), Aerobic and strength training: 3 sessions/week, 30 minutes each, targeting endurance, strength, coordination, mobility, balance, and flexibility Training sessions are self-administered at home, supported by a digital training platform providing instructional videos, and monitored via a wearable activity tracker. Partial supervision is provided through live video-conferencing sessions conducted by a trained exercise therapist in weeks 1, 2, 3, 5, and 7.

Sponsors

Universität Duisburg-Essen
Lead SponsorOTHER

Study design

Allocation
RANDOMIZED
Intervention model
PARALLEL
Primary purpose
SUPPORTIVE_CARE
Masking
NONE

Eligibility

Sex/Gender
ALL
Age
15 Years to No maximum
Healthy volunteers
No

Inclusion criteria

* Diagnosis of bone or soft tissue sarcoma * Currently receiving follow-up care at the tumor orthopedics clinic of University Hospital Essen * Age ≥15 and ≤39 years at time of enrollment * Completion of local tumor therapy (surgery and/or definitive radiotherapy) more than 12 months prior to enrollment * Access to a smartphone for data synchronization with the wearable device

Exclusion criteria

* Contraindications to physical activity * Language barriers preventing communication in German * Known or current psychiatric condition impairing the ability to understand study requirements, participate in the study, or provide informed consent * Pregnancy * Planned absence of more than 2 weeks during the study period (e.g., due to rehabilitation stays) * Pre-existing average MVPA \>60 minutes/day at baseline

Design outcomes

Primary

MeasureTime frameDescription
Moderate-to-Vigorous Physical Activity (MVPA)Baseline (1 week after inlcusion), after 9 weeks and after 13 weeksAverage daily MVPA, measured objectively in minutes/day via wearable activity tracker (Garmin Venu® Sq 2), compared between intervention and control group
Functional Mobility - Stair ClimbingBaseline (1 week after inclusion), after 9 weeks and after 13 weeksTime (in seconds) to ascend and descend 14 stairs (Timed Up and Down Stairs, TUDS)
Functional Mobility - Gait SpeedBaseline (1 week after inclusion), after 9 weeks and after 13 weeksTime (in seconds) to stand up, walk 3 meters, and sit down (Timed Up and Go, TUG)
Functional Exercise CapacityBaseline (1 week after inclusion), after 9 weeks and after 13 weeksDistance walked in 6 minutes (6-Minute Walk Test, 6MWT), measured in meters
Postural BalanceBaseline (1 week after inclusion), after 9 weeks and after 13 weeksTime (in seconds) maintaining single-leg stance on varying surfaces (modified Clinical Test of Sensory Interaction in Balance, CTSIB-M)
Joint Range of MotionBaseline (1 week after inclusion), after 9 weeks and after 13 weeksRange of motion of affected joints, measured in degrees via goniometry
Muscle StrengthBaseline (1 week after inclusion), after 9 weeks and after 13 weeksMuscle strength measured in Newtons via handheld dynamometry
Cardiorespiratory Fitness (VO2peak)Baseline (1 week after inclusion), after 9 weeks and after 13 weeksPeak oxygen uptake (VO2peak in ml/kg/min) assessed via cardiopulmonary exercise testing (spiroergometry)
Left Ventricular Ejection Fraction (LVEF)Baseline (1 week after inclusion), after 9 weeks and after 13 weeksAssessed via transthoracic echocardiography, measured in percent (%)
Resting Heart RateBaseline (1 week after inclusion), after 9 weeks and after 13 weeksAssessed via 12-lead ECG, measured in beats per minute
QTc IntervalBaseline (1 week after inclusion), after 9 weeks and after 13 weeksAssessed via 12-lead ECG, measured in milliseconds

Secondary

MeasureTime frameDescription
Health-Related Quality of Life - Physical Component Summary (SF-36 PCS, Adults)Baseline (1 week after inclusion), after 9 weeks and after 13 weeksPoints on a scale (0-100, higher = better); participants ≥18 years
Health-Related Quality of Life - Mental Component Summary (SF-36 MCS, Adults)Baseline (1 week after inclusion), after 9 weeks and after 13 weeksPoints on a scale (0-100, higher = better); participants ≥18 years
Health-Related Quality of Life - Physical Health Summary Score (Minors, PedsQL)Baseline (1 week after inclusion), after 9 weeks and after 13 weeksPhysical Health Summary Score of the Pediatric Quality of Life Inventory (PedsQL), age-appropriate version (13-18 years), measured in points on a scale (0-100, higher scores indicate better health-related quality of life). Applied to participants \<18 years.
Health-Related Quality of Life - Psychosocial Health Summary Score (Minors, PedsQL)Baseline (1 week after inclusion), after 9 weeks and after 13 weeksPsychosocial Health Summary Score of the Pediatric Quality of Life Inventory (PedsQL), age-appropriate version (13-18 years), calculated as the mean of the Emotional, Social, and School Functioning subscales, measured in points on a scale (0-100, higher scores indicate better health-related quality of life). Applied to participants \<18 years.
Cancer-Related FatigueBaseline (1 week after inclusion), after 9 weeks and after 13 weeksAssessed via the Multidimensional Fatigue Inventory (MFI-20), comprising 5 subscales (General Fatigue, Physical Fatigue, Reduced Activity, Reduced Motivation, Mental Fatigue)
Limb Function (Extremity-Specific)Baseline (1 week after inclusion), after 9 weeks and after 13 weeksLower/upper extremity function assessed via the Toronto Extremity Salvage Score (TESS)
Orthopedic Long-Term ComplicationsBaseline (1 week after inclusion), after 9 weeks and after 13 weeksIncidence of orthopedic complications (e.g., prosthesis-related issues, need for re-operation) recorded during follow-up
Self-Reported Physical Activity (SQUASH)Baseline (1 week after inclusion), after 9 weeks and after 13 weeksSubjectively assessed physical activity level, measured via the Short QUestionnaire to ASsess Health-enhancing physical activity (SQUASH), German version

Contacts

CONTACTIna Elisa Kirchberg, Dr. med.
InaElisa.Kirchberg@uk-essen.de+49 201 723 8084
CONTACTMiriam Götte, Dr. rer. medic.
miriam.goette@uk-essen.de+49 201 723 8083
PRINCIPAL_INVESTIGATORMiriam Götte, Dr. rer. medic.

University Hospital, Essen

PRINCIPAL_INVESTIGATORIna Elisa Kirchberg, Dr. med.

University Hospital, Essen

PRINCIPAL_INVESTIGATORUta Dirksen, Univ.-Prof. Dr. med.

University Hospital, Essen

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Jul 28, 2026