Recruiting

Support Receptivity

Sponsor:

University of Arizona

Code:

NCT07564960

Conditions

Lung Cancer

Eligibility Criteria

Sex: All

Age: 18 - 70+

Healthy Volunteers: Not accepted

Interventions

Social support receptivity training

Social awareness training

Study Details

Brief summary:

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.

Conditions

Lung Cancer

Study ID

NCT07564960

Start date

Apr 27, 2026

Status verified date

Jun, 2026

Completion date

Jul 31, 2026

Anticipated

Primary completion date

Jul 31, 2026

Anticipated

Eligibility Criteria

Eligibility Criteria

Sex: All

Age: 18 - 70+

Healthy Volunteers: Not accepted

Inclusion Criteria:

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

Exclusion Criteria:

1. Less than 12 months of cancer diagnosis at time of enrollment
2. undergoing treatment for mood or anxiety health issues at time of enrollment
3. unable to provide informed consent.

Study Design

Enrollment

30 participants

Anticipated

Allocation

Randomized

Intervention Model

Parallel Assignment

Primary purpose

Supportive Care

Interventions and Outcome Measures

Arms

experimental: Social support receptivity training

Participants will receive a 3-week, 6 session CBT intervention targeting cognitive awareness of prosocial cues coupled with behavioral activation and social skills training to improve target person social engagement.

active comparator: Social awareness training

Participants receiving a 3-week, 6 session program designed to increase awareness of the social support already available to them.

Interventions

Social support receptivity training

A 3-week, 6-session CBT intervention that targets cognitive awareness of prosocial cues and leverages behavioral activation and social skills training

Social awareness training

A 3-week, 6 session program designed to increase awareness of available social support.

Primary outcome measure

  • Feasibility assessed by recruitment and retention rates [ Time Frame: Throughout the recruitment period ]
  • Acceptability assessed by study-specific survey after the intervention [ Time Frame: 3 weeks - immediately after the intervention ]

Central Contacts and Locations

Central contacts

Locations

University of Arizona Mel and Enid Zuckerman College of Public Health

Recruiting

Tucson, Arizona, United States, 85719

Contacts

Principal Investigator:

Scott Carvajal, PhD, MPH

More Information

Sponsor

University of Arizona

Last update posted

Jun 5, 2026

Last verified

Jun, 2026

Keywords

  • Social support
  • Psycho-oncology
  • Lung neoplasms

Trial information was received from ClinicalTrials.gov and was last updated on 2026-09-10. This information was provided to ClinicalTrials.gov by University of Arizona on 2026-06-05.