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NCT07402577Recruiting

Brief Title Mechanisms of Cancer-Related Pain and Opioid Use Among Adolescents and Young Adult Sarcoma Survivors: Pilot Feasibility Study

Source: ClinicalTrials.gov · Last updated 15 Apr 2026

Brief summary (registry, in English)

This study generates information on the feasibility and acceptability of a 3-month ecological momentary assessment (EMA) protocol to assess chronic pain and opioid use in adolescent and young adult (AYA) sarcoma survivors.

Status (registry)
Recruiting
Study type
Observational
Enrollment
40 (estimated)
First submitted
28 Jan 2026
Start date
30 Mar 2026
Primary completion date
1 Feb 2027
Lead sponsor
Roswell Park Cancer Institute
NCT number
NCT07402577

What you commit to

  • Study type: Observational
  • Planned participants: 40
  • From 30 Mar 2026 to the primary completion date, 1 Feb 2027
  • 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

  • \* Currently receiving active cancer-directed therapy.
    • Unable to read or fluently speak English.
    • Determined by clinical staff to have preexisting or cancer-associated cognitive impairment that could interfere with study participation.
    • Acutely suicidal (e.g. intent or plan) or, with unstable medical or psychiatric condition verified by licensed study staff.
    • Characteristics related to inability to complete the study protocol.

Who the study is looking for

  • All genders between the ages of 12-24 (inclusive) at sarcoma diagnosis.
  • Any age \< 70 at the time of study enrollment.
  • No evidence of disease and/or enrolled in survivorship care.
  • Clinically meaningful pain related to disease or its treatments at baseline (defined as 3 or greater on a 0-10 Numerical Rating Scale).
  • Willing to attend the baseline appointment in person.
  • Access to internet-capable smartphone.
  • Access to internet on an occasional basis.
  • Willing and able to complete Ecological Momentary Assessments (EMAs) on internet-capable smartphone for a 3-month period after enrollment.
  • Ability to understand and provide informed consent/assent.

Age in the registry: 12 years to 70 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
Roswell Park Comprehensive Cancer Center
Coordinator of this site? Confirm its status
BuffaloUnited StatesRecruiting

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