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NCT07148193Recruiting

Quality of Life and Medical Care of Long-term Sarcoma Survivors in Germany (PROSa+)

Understanding Long-Term Sarcoma Survivorship: Risk Profiles, Outcomes and Unmet Needs - A Joint Project of Research, Sarcoma Centres and Patient Experts (PROSa+)

Source: ClinicalTrials.gov · Last updated 8 Dec 2025

Brief summary (registry, in English)

The study PROSa+ aims to assess patient-reported outcomes (PROs), patient-reported experiences (PREs), and the socioeconomic situation of long-term sarcoma survivors (≥ 5 years post-diagnosis, with or without active disease) in Germany. The mixed-methods research design includes a multicenter observational study with a cross-sectional questionnaire survey involving 1,600 participants (paper, online), qualitative interviews with up to 60 participants, and longitudinal analyses combining data from existing sarcoma registries and the previous PROSa study conducted between 2017 and 2020.

Status (registry)
Recruiting
Study type
Observational
Enrollment
1600 (estimated)
First submitted
22 Aug 2025
Start date
Nov 2025
Primary completion date
Sept 2027
Lead sponsor
Technische Universität Dresden
Diseases
Sarcoma
NCT number
NCT07148193

What you commit to

  • Study type: Observational
  • Planned participants: 1600
  • From Nov 2025 to the primary completion date, Sept 2027
  • 5 sites 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.

Other illness

  • Inability to complete a structured questionnaire (e.g., due to insufficient German language skills, cognitive impairment, dementia)

Other

  • Diagnosis of Desmoid tumors

Who the study is looking for

  • Diagnosis of sarcoma according to the International Classification of Diseases for Oncology (ICD-O) and World Health Organization (WHO) classification, including soft tissue sarcoma, bone sarcoma, and GIST
  • At least 5 years since initial sarcoma diagnosis
  • With or without active disease
  • Age ≥18 years at the time of study participation

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

Full criteria on ClinicalTrials.gov

Sites (5)

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

SiteCityCountrySite status
Technical University Dresden
Coordinator of this site? Confirm its status
DresdenGermanyRecruiting
University Hospital Essen
Coordinator of this site? Confirm its status
EssenGermanyNot yet recruiting
NCT Heidelberg
Coordinator of this site? Confirm its status
HeidelbergGermanyRecruiting
Sarcoma Center Mannheim
Coordinator of this site? Confirm its status
MannheimGermanyRecruiting
Deutsche Sarkom-Stiftung
Coordinator of this site? Confirm its status
WölfersheimGermanyRecruiting

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