Sign in

NCT07227961Recruiting

Activation Sarcoma: PROMIS and Mobility Evaluation in Sarcoma Patients

Patient-Reported Outcomes and Smartphone-Derived Mobility After Bone and Soft Tissue Sarcoma Surgery: A Multicentre Prospective Cohort Study

Source: ClinicalTrials.gov · Last updated 2 Nov 2026

Brief summary (registry, in English)

Sarcoma is a rare form of bone and soft tissue cancer, making up about 1% of all adult cancers. Management typically involves radiation therapy, chemotherapy, and surgical resection. Surgery is central to the treatment of bone and soft tissue sarcoma, yet post-surgical recovery is difficult to measure because of disease rarity, multiple different tumor types, and treatment variation. Therefore, the overall goal of the study is to use patient reported outcome measures and mobility data to define recovery trajectories in sarcoma patients undergoing surgery, and to evaluate a novel smartphone application (app) entailed Activation Health for collecting these data. Participants will download the Activation Health app on their smartphone. A demographics survey and multiple patient reported outcome measures will be administered remotely through the Activation Health app. Surveys will be completed preoperatively and at 6 weeks, 12 weeks, 6 months 12 months, 16 months, 20 months, and 24 months postoperatively. Additionally, the app will passively track mobility metrics such as daily step count, stairs climbed, and gait parameters throughout the study period. At the end of study participation, an additional surveys will be administered assess participant phone use habits and app function.

Status (registry)
Recruiting
Study type
Observational
Enrollment
800 (estimated)
First submitted
4 Nov 2025
Start date
1 Jul 2025
Primary completion date
30 Jun 2030
Lead sponsor
University of Calgary
Diseases
Sarcoma
NCT number
NCT07227961

What you commit to

  • Study type: Observational
  • Planned participants: 800
  • From 1 Jul 2025 to the primary completion date, 30 Jun 2030
  • 4 sites in 2 countries
  • 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

  • Metastatic bone tumor
  • Diagnosis of atypical lipomatous tumor
  • Diagnosis of dermatofibrosarcoma protuberans
  • Currently pregnant or planning pregnancy within 6 months
  • Unwilling or unable to attend follow-up evaluations
  • Cognitive or communication barriers that impede completion of questionnaires

Who the study is looking for

  • Age ≥ 18 years
  • Diagnosis of bone sarcoma, soft tissue sarcoma, or giant cell tumor of bone
  • Tumors located in the pelvis, lower extremities, or upper extremities
  • Primary or recurrent disease
  • Undergoing operative tumor resection, including limb salvage surgery and amputation
  • Has an iPhone or Android smartphone
  • Speaks English

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

Full criteria on ClinicalTrials.gov

Sites (4)

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

SiteCityCountrySite status
Foothills Medical Centre, Arthur J Child Comprehensive Cancer Centre, University of Calgary
Coordinator of this site? Confirm its status
CalgaryCanadaRecruiting
Mount Sinai Hospital, University of Toronto
Coordinator of this site? Confirm its status
TorontoCanadaRecruiting
Mayo Clinic
Coordinator of this site? Confirm its status
PhoenixUnited StatesNot yet recruiting
Mayo Clinic
Coordinator of this site? Confirm its status
RochesterUnited StatesNot yet recruiting

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