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NCT07564960Recruiting

Social Optimization Study

Improving the Lives of Cancer Survivors Through Enhancing Support Receptivity

Source: ClinicalTrials.gov · Last updated 21 Sept 2026

Brief summary (registry, in English)

This study tests whether clinical interventions to optimize support receptivity lead to improvements in social integration and quality of life (QOL) amongst long-term lung cancer survivors. The feasibility and acceptability of the intervention and assessment procedures will be examined. Thirty long-term lung cancer survivors will be randomized to a support receptivity intervention or an attention-control condition. Our intervention draws on cognitive behavioral therapy (CBT) strategies to reduce social anxiety, improve social awareness, and promote social integration. We will use two novel in vivo sampling methods using a mobile phone platform to assess social engagement and QOL improvements: 1) recording via the Electronically Activated Recorder to capture daily social interactions, and 2) repeated self-report sampling where participants answer questions about their social engagement experiences via their personal cell phone.

Status (registry)
Recruiting
Study type
Interventional
Enrollment
30 (estimated)
First submitted
27 Apr 2026
Start date
Apr 2026
Primary completion date
Oct 2026
Lead sponsor
University of Arizona
Diseases
Lung cancer
NCT number
NCT07564960

What you commit to

  • Study type: Interventional
  • Planned participants: 30
  • From Apr 2026 to the primary completion date, Oct 2026
  • 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.

Other illness

  • Less than 12 months of cancer diagnosis at time of enrollment

Other

  • undergoing treatment for mood or anxiety health issues at time of enrollment
  • unable to provide informed consent.

Who the study is looking for

  • Adults (18 Years or Older)
  • History of lung cancer
  • at least 12 months since cancer diagnosis
  • fluent in English
  • able to attend virtually or in person sessions at the University of Arizona.

Age in the registry: 18 years to 99 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
University of Arizona Mel and Enid Zuckerman College of Public Health
Coordinator of this site? Confirm its status
TucsonUnited StatesRecruiting

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