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An Open Trial of Telephone-Delivered Mindfulness-Based Cognitive Therapy: Feasibility, Acceptability, and Preliminary Efficacy for Reducing Depressive Symptoms.

Amanda J Shallcross, Zoe T Duberstein, Sarah H Sperber, Pallavi Visvanathan, Samina Lutfeali, Nathaniel Lu, James Carmody, Tanya M Spruill

Cognitive and Behavioral Practice May 2022 DOI: 10.1016/j.cbpra.2020.12.004 (opens in new tab)

Study at a glance

AI-extracted from the abstract
Characteristics Pilot trial Pilot study Peer reviewed
Sample size 14
Population Patients with mild to moderate depressive symptoms and hypertension (78.6% female, mean age 60.6)
Intervention Mindfulness-based cognitive therapy
Duration 8-week intervention; assessments at baseline and immediately postintervention
Measures Quick Inventory of Depressive Symptomatology-Self-Report (QIDS-SR), Hospital Anxiety and Depression Scale-Anxiety subscale (HADS-A)
Topics Depression Meditation
Keywords Hypertension Mindfulness-based cognitive therapy Pilot trial Telephone-delivered
Key findings The abbreviated, telephone-delivered MBCT program was feasible and acceptable in this small sample: 64% attended at least four sessions, satisfaction was high, and no adverse events occurred. Depressive symptom scores decreased by 4.09 points and anxiety scores by 3.18 points postintervention, which the authors describe as preliminary evidence of efficacy.

Abstract

Mindfulness-based cognitive therapy (MBCT) is a promising intervention for reducing depressive symptoms in individuals with comorbid chronic disease, but the program's attendance demands make it inaccessible to many who might benefit. We tested the feasibility, acceptability, safety, and preliminary efficacy of an abbreviated, telephone-delivered adaptation of the in-person mindfulness-based cognitive therapy (MBCT-T) program in a sample of patients with depressive symptoms and hypertension. Participants (n = 14; 78.6% female, mean age = 60.6) with mild to moderate depressive symptoms and hypertension participated in the 8-week MBCT-T program. Feasibility was indexed via session attendance and home-based practice completion. Acceptability was indexed via self-reported satisfaction scores. Safety was assessed via reports of symptomatic decline or need for additional mental health treatment. Depressive symptoms (Quick Inventory of Depressive Symptomatology-Self-Report [QIDS-SR]) and anxiety (Hospital Anxiety and Depression Scale-Anxiety subscale; HADS-A) were assessed at baseline and immediately following the intervention. Sixty-four percent of participants (n = 9) attended ≥4 intervention sessions. Seventy-one percent (n = 6) of participants reported completing all assigned formal home practice and 89.2% (n = 8) reported completing all assigned informal practice. Participants were either very satisfied (75%; n = 6) or mostly satisfied (25%; n = 2) with the intervention. There were no adverse events or additional need for mental health treatment. Depressive symptom scores were 4.09 points lower postintervention (p = .004). Anxiety scores were 3.18 points lower postintervention (p = .039). Results support the feasibility, acceptability, safety, and preliminary efficacy of an abbreviated, telephone-delivered version of MBCT for reducing depressive and anxiety symptoms in individuals with co-occurring chronic disease.

Comparable studies

Other non-randomized and open-label trials on meditation, most cited first.

Study Year Design Participants
Mindfulness-Based Stress Reduction in Relation to Quality of Life, Mood, Symptoms of Stress, and Immune Parameters in Breast and Prostate Cancer Outpatients Early-stage breast and prostate cancer patients 2003 Pre-post intervention study n = 59
Exploring self‐compassion and empathy in the context of mindfulness‐based stress reduction (MBSR) Community sample 2010 Pre-post intervention study
Mindfulness-Based Stress Reduction Lowers Psychological Distress In Medical Students Second-year medical students 2003 Prospective nonrandomized cohort-controlled study n = 302
Intensive meditation training, immune cell telomerase activity, and psychological mediators. Retreat participants and matched controls 2011 Controlled trial with wait-list control group n = 60
The Effectiveness of Mindfulness Training for Children with ADHD and Mindful Parenting for their Parents Children aged 8-12 with ADHD and their parents 2011 Within-group waitlist controlled trial n = 22

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