Skip to main content
Clinical Trials/NCT01476891
NCT01476891
Unknown
Not Applicable

The eCALM Study - eTherapy for Cancer Applying Mindfulness: Online Mindfulness-Based Stress Reduction Program for Underserved Cancer Patients in Alberta: A Randomized Wait-list Controlled Trial.

Alberta Health services1 site in 1 country64 target enrollmentJanuary 2011

Overview

Phase
Not Applicable
Intervention
Not specified
Conditions
Mindfulness-Based Stress Reduction (MBSR)
Sponsor
Alberta Health services
Enrollment
64
Locations
1
Primary Endpoint
Feasibility
Last Updated
13 years ago

Overview

Brief Summary

For people with cancer, in-person Mindfulness-Based Stress Reduction (MBSR) participation can decrease stress symptoms, mood disturbance, and fatigue, as well as enhance personal growth and spirituality, and improve quality of life and sleep. Online MBSR may improve the accessibility of MBSR programs to underserved cancer patients who are unable to attend available in-person groups. This study will examine whether patients are willing to participate and complete the program, and also whether the online program improves mood and stress.

Registry
clinicaltrials.gov
Start Date
January 2011
End Date
August 2014
Last Updated
13 years ago
Study Type
Interventional
Study Design
Parallel
Sex
All

Investigators

Responsible Party
Sponsor

Eligibility Criteria

Inclusion Criteria

  • 18 years of age or older
  • Speak and read English sufficiently to complete questionnaires
  • Women and men who have been diagnosed with any type of cancer, at any time in the past with no restriction on tumor site
  • Pre or post primary cancer treatment, up to having completed primary cancer treatment within the last 36 months
  • Exhibiting moderate distress
  • Willing to participate in the intervention requirements; able to participate in the intervention (2 hrs per week for 8 weeks and a full day online retreat)
  • Internet access
  • Resident of Alberta, who has limited access to in-person cancer-specific MBSR programs

Exclusion Criteria

  • Presence of major self-reported psychiatric disorder not in remission, current substance abuse/dependence, and psychotic symptoms
  • Previous participation in a MBSR program

Outcomes

Primary Outcomes

Feasibility

Time Frame: 44 months

recruitment, retention, attendance, adherence, satisfaction

Secondary Outcomes

  • Efficacy(44 months)
  • Post-Traumatic Growth Inventory (PTGI)(44 months)
  • Functional Assessment of Chronic Illness Therapy - Spiritual Well-Being (FACIT-Sp)(44 months)
  • Five Facet Mindfulness Questionnaire (FFMQ)(44 months)

Study Sites (1)

Loading locations...

Similar Trials