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Proactive Care Coordination for Cancer Survivors Who Smoke

NYU Langone Health logo

NYU Langone Health

Status

Completed

Conditions

Cancer

Treatments

Behavioral: Online Referral NYS Quitline
Behavioral: Tobacco cessation counseling and coordination of cessation medications

Study type

Interventional

Funder types

Other

Identifiers

NCT02723656
15-01069

Details and patient eligibility

About

This is a population-based randomized controlled trial of 600 patients with a diagnosis of cancer in the past 2 years and registry indicating smoking at the time of diagnosis, that will inform critical questions regarding the relative efficacy of care coordination options, the reliability of Electronic Health Record (EHR) tobacco use data, and how patients will react to proactive tobacco related communications. Investigators will compare the reach and efficacy of two proactive approaches to enrolling cancer survivors in tobacco treatment (Arm 1: mailed care coordination vs. Arm 2: telephone care coordination) using a two-arm randomized design at two urban cancer centers, and will explore cancer survivor attitudes and preferences about proactive tobacco treatment.

Enrollment

581 patients

Sex

All

Ages

18+ years old

Volunteers

No Healthy Volunteers

Inclusion criteria

  • ICD 9 cancer diagnosis seen at each site in the past two years
  • Documentation of current smoking in the cancer registry.

Exclusion criteria

  • Dementia
  • Stage IV or Stage IIIB cancer

Trial design

Primary purpose

Supportive Care

Allocation

Randomized

Interventional model

Parallel Assignment

Masking

None (Open label)

581 participants in 2 patient groups

Proactive mailed care coordination
Active Comparator group
Treatment:
Behavioral: Online Referral NYS Quitline
Proactive telephone care coordination.
Active Comparator group
Treatment:
Behavioral: Tobacco cessation counseling and coordination of cessation medications

Trial contacts and locations

1

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Data sourced from clinicaltrials.gov

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