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N/A N=18 Supportive Care

Resilience Measurement in Older Adults With Late-Stage Lung Cancer

Lung Cancer Stage III · Lung Cancer Stage IV

Enrolled (actual)
18
Serious AEs
0.0%
Results posted
Feb 2024
Primary outcome: Primary: Confidence in Behavior as Measured by the Cancer Behavior Inventory — 80.89; 85.92; 93.23 score on a scale

Study Design & Population

Study type
Interventional
Phase
N/A
Interventions
Self System Therapy for Older Adults with Advanced Lung Cancer (SST-LC) Resilience (Behavioral)
Age
Older Adult · 65+ yrs
Sex
All
Sponsor
Duke University
Primary completion
Mar 2022

Outcome Measures

OutcomeResultp-value
PRIMARY
Confidence in Behavior as Measured by the Cancer Behavior Inventory
80.89; 85.92; 93.23
SECONDARY
Coping Skills Related to Stress as Measured by the Brief COPE (Coping Orientation to Problems Experienced)
55.72; 58.54; 57.62
SECONDARY
Resilience as Measured by the CD-RISC-25 (Connor-Davidson Resilience Scale)
73.16; 75.69; 78.00
SECONDARY
Depression as Measured by the Beck Depression Inventory (BDI-II)
9.06; 7.92; 8.23
SECONDARY
Positive Affect as Measured by the PANAS (Positive and Negative Scale)
32.72; 34.61; 36.15
SECONDARY
Negative Affect as Measured by the PANAS (Positive and Negative Scale)
18.04; 17.31; 17.54
SECONDARY
Physical Activity as Measured by the PASE (Physical Activity Scale for the Elderly)
101.06; 110.23; 109.17
SECONDARY
Pain Interference as Measured by the PROMIS PI (Patient-Reported Outcomes Measurement Information System Pain Interference)
SECONDARY
Number of Participants Who Completed the QUALE (Quality of Life at the End of Life)
18; 13; 13

Summary

The purpose of this study to test measures of physical and psychological resilience while using Self-System therapy (SST), to treat depression and lung-cancer-related distress in older adults (65 years and older).

Eligibility Criteria

Inclusion Criteria

  • Age 65 or older
  • English-speaking
  • The patient has a diagnosis of late-stage (III-IV) lung cancer and is living at his/her home.

Exclusion Criteria

  • Unable to provide informed consent
  • Visual or hearing impairments that preclude participation
  • Serious mental illness
View full record on ClinicalTrials.gov →

Data sourced from ClinicalTrials.gov (NCT04825912). Outcome figures and adverse-event rates are extracted automatically from the registry's posted results and are provided for clinician reference, not as a substitute for the primary publication.

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