CompletedInterventionalPhase 1Phase 2Updated May 7, 2014
Enhancing Coping Skills in Patients With Cancer | NCT01359072 | Trialant
TerminatedInterventionalNot ApplicableUpdated Aug 22, 2012
Enhancing Coping Skills in Patients With Cancer
Enhancing Coping Skills in Patients With Cancer - a Randomized Controlled Study
ClinicalTrials.gov ID
NCT01359072
Lead Sponsor
McGill University Health Centre/Research Institute of the McGill University Health CentreOTHER
Overall Status
Terminated
Study Type
Interventional
Phase
Not Applicable
Enrollment
1Actual
Last Update Posted
Aug 22, 2012Estimated
Start Date
Jun 2011
Primary Completion Date
Aug 2012Actual
Completion Date
Aug 2012Actual
Official Title
Enhancing Coping Skills in Patients With Cancer - a Randomized Controlled Study
Brief Summary
Approximately 30% of all patients with cancer report levels of psychological distress indicative of the need for psychological intervention.
Research suggests that learning more adaptive coping strategies improves psychological adjustment to cancer.
It is imperative to develop cost-efficient, feasible psychosocial interventions.
The aim is to test the efficacy of the self administered format of a psycho-educational intervention (NUCARE) in reducing distress and enhancing adaptive coping strategies for cancer patients.
It is hypothesized that:
patients would show significant reductions in distress (i.e., depression and anxiety) over the 6-week treatment period, and that treatment would produce superior results compared to wait-list; patients would maintain or even increase their improvement up to 3 months following treatment.
the treatment would enhance more adaptive coping strategies.
greater self-reported adherence to the treatment/homework would be associated with symptom improvement, more autonomous self-regulation and higher perceived competence for adhering to the coping intervention program.
Cancer
Self administered coping intervention
Ages Eligible for Study
Adult (18-64)Older Adult (65+)
Sexes Eligible for Study
All
Accepts Healthy Volunteers
No
Eligibility Criteria
Inclusion Criteria:
18+ years of age,
able to read English,
a cancer patient presenting at the McGill University Health Centre (MUHC) interested in participating,
willing to receive minimal therapist contact (by telephone) and self administered therapy,
able to give their own consent.
Exclusion Criteria:
currently receiving psychological/psychiatric treatment/counselling,
indicate at the time of recruitment that they intend to seek psychological treatment elsewhere during the study period,
a history of psychosis or bipolar disorder,
substance abuse/dependence in last 6 months,
taking psychotropic medication with altering dosages in the past 3 months.
Primary Purpose
Treatment
Allocation
Randomized
Interventional Model
Parallel Assignment
Masking
Single
No central contacts
There are no central contacts for this study.
McGill University Health Centre - Melanoma Clinic & Cedars CanSupport
Montreal, Quebec H3A 1A1, Canada
Lead Sponsor
McGill University Health Centre/Research Institute of the McGill University Health CentreOTHER
Collaborators
Louise Granofsky-Psychosocial Oncology Program, Segal Cancer Centre, MontrealUNKNOWN