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Clinical Trials/NCT00967083
NCT00967083
Completed
Not Applicable

Support Needs and Preferences of Family Caregivers of Lung Cancer Patients

Memorial Sloan Kettering Cancer Center2 sites in 1 country53 target enrollmentAugust 2009
ConditionsLung Cancer

Overview

Phase
Not Applicable
Intervention
Not specified
Conditions
Lung Cancer
Sponsor
Memorial Sloan Kettering Cancer Center
Enrollment
53
Locations
2
Primary Endpoint
Assess psychosocial info & practical needs of prim family caregivers of lung cancer pts.Mental health (anxiety & depression)& behavioral health needs(smoking cessation,alcohol abuse)will be assessed b/c these 2 types of needs are strongly correlate
Status
Completed
Last Updated
11 years ago

Overview

Brief Summary

This study is being done to learn what the needs are in relation to the family members. Some family members seek counseling; others do not. The institution wants to try to understand why and wants to see if they can improve our support services for family members.

Registry
clinicaltrials.gov
Start Date
August 2009
End Date
December 2014
Last Updated
11 years ago
Study Type
Observational
Sex
All

Investigators

Responsible Party
Sponsor

Eligibility Criteria

Inclusion Criteria

  • Primary family caregiver identified by a patient who is approximately within 4 to 6 weeks of a new visit to a thoracic clinic and receiving cancer care at Memorial Sloan-Kettering Cancer Center or Queens Cancer Center
  • Caregiver is at least 18 years of age.
  • Caregiver has adequate English fluency for completion of data collection. The surveys were designed and validated in English and are not currently available in other languages. Translation of questionnaires into other languages would require reestablishing the reliability and validity of these measures. Therefore, participants must be able to communicate in English to complete the surveys.
  • Clinically meaningful distress defined as a score of 8 or greater on the Anxiety or Depression subscale of the HADS (see Bjelland et al., 2002; Zigmond \& Snaith, 1983).

Exclusion Criteria

  • Patients or caregivers exhibiting significant psychiatric or cognitive impairment (dementia/delirium, retardation, active psychosis) that in the judgment of the investigators would preclude providing informed consent and study participation
  • Patient has lung cancer recurrence
  • Currently participating in a psychosocial intervention trial

Outcomes

Primary Outcomes

Assess psychosocial info & practical needs of prim family caregivers of lung cancer pts.Mental health (anxiety & depression)& behavioral health needs(smoking cessation,alcohol abuse)will be assessed b/c these 2 types of needs are strongly correlate

Time Frame: 13 to 16 weeks

Secondary Outcomes

  • To assess psychosocial and practical barriers to psychosocial support service use among primary family caregivers of lung cancer patients(13 to 16 weeks)
  • To assess family caregivers' preferences (preferred topics, modality, provider, timing) regarding psychosocial support interventions.(13 to 16 weeks)
  • To gather descriptive information regarding participant flow for planning future intervention studies.(13 to 16 weeks)

Study Sites (2)

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