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Clinical Trials/NCT02353546
NCT02353546CompletedNot Applicable

Managing Cancer and Living Meaningfully (CALM): Phase 2b Pilot Randomized Psychotherapy Trial in Patients With Advanced Cancer

University Health Network, Toronto1 site in 1 country60 target enrollmentStarted: June 1, 2011Last updated:
Conditions
Interventions

Trial Snapshot

Phase
Not Applicable
Status
Completed
Enrollment
60
Locations
1
Primary Endpoint
Patient Health Questionnaire-9 (PHQ-9)

Study Overview

Brief Summary

Managing Cancer And Living Meaningfully (CALM) is a brief psychotherapy designed to alleviate distress in advanced cancer. In an earlier intervention-only pilot trial, CALM was associated with reductions in depressive symptoms and death anxiety and an increase in spiritual wellbeing. The purpose of this study is to assess the feasibility of a large-scale randomized controlled trial (RCT) of CALM and to identify preliminary effects in advanced cancer. This phase 2b pilot RCT employed intervention and usual care arms with 3 and 6 month follow-ups. The primary outcome was depressive symptoms (PHQ-9) and secondary outcomes included diagnosis of major depression (SCID), death anxiety, attachment security and spiritual wellbeing. Multilevel regression was used to compare change over time between groups. 60 patients with advanced cancer will be recruited from the Princess Margaret Cancer Centre, Toronto, Canada, and equally randomized into intervention and usual care conditions.

Detailed Description

Abstract

Background Managing Cancer And Living Meaningfully (CALM) is a brief individual psychotherapy for patients with advanced cancer. In an intervention-only phase 2a trial, CALM showed promising results, leading to the present 2b pilot, which introduces procedures for randomisation and improved rigour in preparation for a phase 3 randomised controlled trial (RCT).

Aims To test trial methodology and assess feasibility of a confirmatory RCT.

Design A parallel-arm RCT (intervention vs usual care) with 3 and 6-month follow-ups. Assessment of feasibility included rates of consent, randomisation, attrition, intervention non-compliance and usual care contamination. Primary outcome: depressive symptoms (Patient Health Questionnaire-9; PHQ-9). Secondary outcomes: major depressive disorder (MDD), generalised anxiety, death anxiety, spiritual well-being, attachment anxiety and avoidance, self-esteem, experiential avoidance, quality of life and post-traumatic growth. Bayesian conjugate analysis was used in this low-powered setting.

Setting/participants 60 adult patients with advanced cancer from the Princess Margaret Cancer Centre.

Study Design

Study Type
Interventional
Allocation
Randomized
Intervention Model
Parallel
Primary Purpose
Treatment
Masking
None

Eligibility Criteria

Ages
18 Years to — (Adult, Older Adult)
Sex
All
Accepts Healthy Volunteers
No

Inclusion Criteria

  • •18 years of age or older
  • •Fluent in English
  • •Confirmed diagnosis of Stage IIIB or IV lung cancer, Stage III or IV ovarian cancer, Stage IV endocrine, breast, gastrointestinal, genitourinary or gynecologic cancer, or pancreatic cancer at any stage

Exclusion Criteria

  • •Short Orientation-Memory-Concentration Test (score of <20)
  • •Individuals receiving in-hospital psychiatric or psychological treatment at the time of recruitment

Arms & Interventions

CALM

Experimental

Patients assigned to the intervention arm will receive 3-6 CALM therapy sessions over 3-6 months delivered by a trained therapist at our center.

Intervention: CALM (Behavioral)

Usual Care

No Intervention

Outcomes

Primary Outcomes

Patient Health Questionnaire-9 (PHQ-9)

Time Frame: 6-months

Secondary Outcomes

  • Generalized Anxiety Disorder-7 (GAD-7)(6-months)
  • Functional Assessment of Chronic Illness Therapy-Spiritual Well-being Scale (FACIT-Sp-12)(6-months)
  • Acceptance and Action Questionnaire-II (AAQ-II)(6-months)
  • Death and Dying Distress Scale (DADDS)(6-months)
  • Quality of Life at the End of Life-Cancer Scale (QUAL-EC)(6-months)
  • Major Depression Structured Clinical Interview for DSM Disorders (SCID)(6-months)
  • Posttraumatic Growth Inventory (PTGI)(6-months)
  • Modified Experiences in Close Relationships (ECR M-16)(6-months)
  • Rosenberg Self-esteem Scale (RSES)(6-months)

Investigators

Sponsor Class
Other
Responsible Party
Sponsor

Study Sites (1)

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