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Clinical Trials/NCT05048316
NCT05048316
Completed
N/A

Pilot Study to Develop a Group-Based E-Health Intervention for Young Adult Cancer Survivors

H. Lee Moffitt Cancer Center and Research Institute1 site in 1 country17 target enrollmentMay 11, 2021

Overview

Phase
N/A
Intervention
Not specified
Conditions
Cancer Survivor
Sponsor
H. Lee Moffitt Cancer Center and Research Institute
Enrollment
17
Locations
1
Primary Endpoint
Session attendance after the intervention - Acceptability
Status
Completed
Last Updated
3 years ago

Overview

Brief Summary

Investigators will test an evidence-based behavioral intervention that is responsive to Young Adults (YA's) expressed needs and priorities

Registry
clinicaltrials.gov
Start Date
May 11, 2021
End Date
January 6, 2022
Last Updated
3 years ago
Study Type
Interventional
Study Design
Single Group
Sex
All

Investigators

Eligibility Criteria

Inclusion Criteria

  • 18-39 years old
  • Diagnosed with cancer between 18-39 years old
  • Cancer diagnosis was non-metastatic
  • Completed cancer treatment between 1 month and 5 years prior to enrollment, with the exception of ongoing hormone therapy
  • No documented or observable psychiatric or neurological disorders that could interfere with participation (e.g., active psychosis, active substance abuse), as identified by the referring medical team, chart review, or screening
  • Able to speak and read English
  • Able to provide informed consent

Exclusion Criteria

  • Metastatic disease
  • Continued cancer treatment
  • Psychiatric or neurological disorders that could interfere with study participation
  • Vulnerable populations will not be included

Outcomes

Primary Outcomes

Session attendance after the intervention - Acceptability

Time Frame: Immediately after the intervention

Videoconference delivery will be acceptable if average group attendance is ≥6/10 sessions.

Satisfaction assessed by study-specific survey during the intervention - Acceptability

Time Frame: During intervention

The intervention will be deemed acceptable if, on average, participants report satisfaction with the weekly sessions as ≥2 on a 0-4 scale.

Satisfaction assessed by study-specific survey after the intervention - Acceptability

Time Frame: Immediately after the intervention

The intervention will be deemed acceptable if, on average, participants report satisfaction with the overall program and intent to continue using the intervention skills as ≥2 on a 0-4 scale.

Secondary Outcomes

  • Quality of life before intervention(Baseline)
  • Change in quality of life at after intervention(Immediately after intervention)

Study Sites (1)

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