CompletedNot applicableNCT02575898

Feasibility of a Creative Writing Intervention in an Advanced Cancer Population: A Single Arm, Consecutive Cohort Study

To assess the feasibility of a creative writing intervention in an advanced cancer population. Given it is a relatively simple intervention delivered by a non-clinician, the investigators are interested in better understanding its pattern of effect on patient psychological adjustment. The investigators aim to assess its feasibility in this study in order to inform a future larger study that will utilize a control arm.

Checked against the public recordLast updated Nov 19, 2018 · Source: ClinicalTrials.gov

StatusCompleted
PhaseNot applicable
U.S. locations1
SponsorDartmouth-Hitchcock Medical Center
01
Study overview

What this study is about

Purpose
Supportive Care
Study type
Interventional
Phase
Not applicable
Sponsor
Dartmouth-Hitchcock Medical Center
Interventions being studied
Other: First Session; Other: Second Session; Behavioral: Third through Sixth Sessions
02
Explore related studies

How this study is categorized

These labels come from structured fields and exact terms in the public record.

03
Public criteria

Who may be able to participate

Inclusion Criteria: 1. Participant must plan to receive follow up care at Dartmouth-Hitchcock. 2. Participant must have a lung or GI primary cancer diagnosed in the last 3 months. 3. Participant must have non-curable cancer as judged by the primary oncologist. 4. Participant must be comfortable conversing in English (reading and writing in English is not required). 5. Participant must be cognitively intact as judged by their responsible clinician. 6. Participant must have access to a working telephone and be willing and available to participate by this modality as needed. 7. Participants may be on anti-depressants and/or anxiolytics as long as the dosing has remained stable over the preceding 2 weeks. Exclusion Criteria: 1. Participant is expected to die in 6 months or less as judged by the responsible clinician. 2. Participant must not have already worked with the staff writer at Dartmouth Hitchcock prior to enrollment in this study. 3. Participant with an activated durable power of attorney for health care or cognitive impairment that interferes with ability to understand prognosis as determined by the primary oncologist. 4. Participant must not have uncontrolled physical symptoms.

Important: This is the sponsor’s public criteria, not a determination of eligibility. The study team must review your individual situation.

04
Study sites

U.S. locations

  • Dartmouth-Hitchcock Medical CenterLebanon, New Hampshire

Source and freshness
Processed from ClinicalTrials.gov. Last public update: Nov 19, 2018. Always confirm current availability with the study team.

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