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Personalized Exercise Oncology

Personalized Exercise Oncology (PEXO) - Study

Status
Active, not recruiting
Phases
Unknown
Study type
Observational
Source
ClinicalTrials.gov
Registry ID
NCT04328038
Acronym
PEXO
Enrollment
800
Registered
2020-03-31
Start date
2018-11-26
Completion date
2026-02-28
Last updated
2025-02-03

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

Conditions

Cancer, Health Behavior

Keywords

Physical Activity, Exercise, Health literacy, cancer-related symptoms, treatment-related symptoms, personalized Medicine

Brief summary

The Goal of the study is to identify trait-homogenous groups of cancer patients in regards to their physical activity associated health literacy. Based on these Groups, individualized exercise protocols and educative strategies can be developed which may increase the efficacy of the exercise therapy and increases the likelihood that patient get involved in physical activity.

Interventions

OTHERSurvey

Patient fill out a survey containing: Demographic Information, medical history, several Questionnaires about Health Literacy, Well Being/HRQoL and Fatigue

Sponsors

Penn State University
CollaboratorOTHER
University Hospital Heidelberg
Lead SponsorOTHER

Study design

Observational model
COHORT
Time perspective
CROSS_SECTIONAL

Eligibility

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

Inclusion criteria

* Histologically confirmed cancer diagnosis * Females and males ≥18 years of age * Undergoing either chemo-, immune-, radio- or anti-hormonal treatment * Last surgery more than 6 weeks in the past * Ability to understand English or German * Be able to provide and understand informed consent * Have an Eastern Cooperative Oncology Group (ECOG) Performance Score of ≤ 2

Exclusion criteria

* Heart insufficiency \> NYHA III (New York Heart Association) or uncertain arrhythmia * Uncontrolled hypertension * Severe renal dysfunction (GFR \< 30%, Creatinine\> 3mg/dl) * Reduced standing or walking * Current pregnancy * Any other evidence in the medical record of an absolute contraindication for exercise

Design outcomes

Primary

MeasureTime frameDescription
Patient Clustersthrough study completion, an average of 1 yearIdentification of different, trait-homogenous patient clusters

Secondary

MeasureTime frameDescription
Questionnaire: Health Literacythrough study completion, an average of 1 yearTo assess health-literacy the recently developed and validated questionnaire from Sudeck and Pfeifer (2016) will be used
Questionnaire: Health Related Quality of Lifethrough study completion, an average of 1 yearQuality of Life will be assessed with the validated 30-item self-assessment questionnaire of the European Organization for Research and Treatment of Cancer (EORTC QLQ-C30, version 3.0).
Questionnaire: Fatiguethrough study completion, an average of 1 yearTo asses fatigue patients will be asked to complete the 12-item EORTC QLQ-FA12 (FA = fatigue), which is a newly developed questionnaire which has been intensively validated
Questionnaire: Physical Activity Associated Health Literacythrough study completion, an average of 1 yearTo assess physical activity-associated health competence the recently developed and validated questionnaire from Sudeck and Pfeifer (2016) will be used
Questionnaire: Emotion Thermometersthrough study completion, an average of 1 yearEmotion thermometers are four-domain visual-analogue scale including distress, anxiety, depression, and anger. Each domain is rated on an 11-point (0 to 10) Likert scale
Questionnaire: Brief Pain Inventory (BPI)through study completion, an average of 1 yearBone pain will be assessed with the Brief Pain Inventory (BPI). This is a valid and reliable tool for pain measurement in cancer patients with bone metastases. It measures both pain severity and pain interference on function
Questionnaire: Physical Activitythrough study completion, an average of 1 yearPatient's level of physical activity will be assessed with the SQUASH Physical Activity Questionnaire. It includes multiple activities referring to a 'normal' week. Activity dimensions asked include actively commuting physical activity (walking, cycling), physical activity at work or school, household activities, leisure time activities (sports, walking, gardening, cycling).

Countries

Germany

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 9, 2026