Bibliotherapy for Patients With Cancer

This study is currently recruiting participants.
Verified March 2013 by McGill University Health Center
Sponsor:
Collaborator:
Cedars CanSupport, Hope & Cope
Information provided by (Responsible Party):
Dr. Annett Korner, PhD, McGill University Health Center
ClinicalTrials.gov Identifier:
NCT01718574
First received: October 24, 2012
Last updated: March 14, 2013
Last verified: March 2013
  Purpose

The purpose of this study is to examine the efficacy of a self-help workbook in enhancing a sense of empowerment, coping, quality of life and reducing distress for patients with cancer.


Condition Intervention
Cancer
Other: Self-help book

Study Type: Interventional
Study Design: Allocation: Randomized
Intervention Model: Parallel Assignment
Masking: Open Label
Primary Purpose: Supportive Care
Official Title: Feasibility, Acceptability and Efficacy of Bibliotherapy for Patients With Cancer: a Randomized Control Trial

Resource links provided by NLM:


Further study details as provided by McGill University Health Center:

Primary Outcome Measures:
  • change in Health Education Impact Questionnaire scores [ Time Frame: pre-intervention (week 0), post intervention (week 6), follow-up (week 10) ] [ Designated as safety issue: No ]

Secondary Outcome Measures:
  • change in Ways of Coping Questionnaire - Cancer Version & Hospital Anxiety and Depression Scale scores [ Time Frame: pre-intervention (week 0), post intervention (week 6), follow-up (week 10) ] [ Designated as safety issue: No ]

Estimated Enrollment: 102
Study Start Date: February 2013
Arms Assigned Interventions
Experimental: Self-help book Other: Self-help book
Participants have 6 weeks to complete a 12 chapter self-help workbook. The workbook addresses: (i) The enhancement of a sense of personal control; and (ii) The learning of emotional and instrumental coping responses
No Intervention: Usual Care Control

  Eligibility

Ages Eligible for Study:   18 Years and older
Genders Eligible for Study:   Both
Accepts Healthy Volunteers:   No
Criteria

Inclusion Criteria:

  • 18+ years of age
  • been diagnosed with cancer
  • can read English

Exclusion Criteria:

-participating in the "Think Smart, Live Well" group

  Contacts and Locations
Please refer to this study by its ClinicalTrials.gov identifier: NCT01718574

Contacts
Contact: Annett Korner, PhD 514-398-2481 annett.koerner@mcgill.ca
Contact: Nicole Roberts, M.Ed nicole.roberts@mail.mcgill.ca

Locations
Canada, Quebec
MUHC Cedars CanSupport Recruiting
Montreal, Quebec, Canada, H3A 1A1
Hope & Cope, JGH Recruiting
Montreal, Quebec, Canada
Sponsors and Collaborators
McGill University Health Center
Cedars CanSupport, Hope & Cope
  More Information

No publications provided

Responsible Party: Dr. Annett Korner, PhD, Principal Investigator, McGill University Health Center
ClinicalTrials.gov Identifier: NCT01718574     History of Changes
Other Study ID Numbers: 2888
Study First Received: October 24, 2012
Last Updated: March 14, 2013
Health Authority: Canada: Ethics Review Committee

Keywords provided by McGill University Health Center:
self-help book
support service

ClinicalTrials.gov processed this record on April 22, 2014