A telephonic mindfulness-based intervention for persons with sickle cell disease: study protocol for a randomized controlled trial.
Study Goal
The researchers aimed to evaluate the acceptability, feasibility, and preliminary efficacy of a telephonic mindfulness-based intervention (MBI) for adults with sickle cell disease (SCD) and chronic pain.
Results Summary
The study protocol outlines a randomized controlled trial to assess the MBI's impact on pain catastrophizing, with feasibility, acceptability, and efficacy measured via questionnaires and interviews. Results are pending as the abstract describes the study design rather than outcomes.
Population
Adults with sickle cell disease (SCD) and chronic pain in the southeastern United States.
Effective Dosage
Six sessions (60 minutes each) of telephonic group-based MBI.
Duration
6 weeks (one session per week).
Interactions
None mentioned
| Intervention | Direction | Endpoint | Population | Dosage | Impact | Claim # |
|---|---|---|---|---|---|---|
mindfulness-based interventions (MBIs) | decrease | both physical and affective components of pain | persons with sickle cell disease (SCD) | - | promising category of nonpharmacological interventions for managing | #1 |
telephonic MBI | neutral | acceptability, feasibility, and preliminary efficacy | adults with SCD who have chronic pain | - | evaluate the acceptability and feasibility, as well as to determine the preliminary efficacy | #2 |
six-session (60 minutes), telephonically delivered, group-based MBI program | decrease | pain catastrophizing | adult patients with SCD and chronic pain | - | feasibility, acceptability, and efficacy of the MBI regarding | #3 |
BACKGROUND: One of the most difficult symptoms for persons with sickle cell disease (SCD) to manage is chronic pain. Chronic pain impacts approximately one-third of persons with SCD and is associated with increased pain intensity, pain behavior, and frequency and duration of hospital visits. A promising category of nonpharmacological interventions for managing both physical and affective components of pain are mindfulness-based interventions (MBIs). METHODS/DESIGN: The primary aim of this study is to conduct a randomized controlled study to evaluate the acceptability and feasibility, as well as to determine the preliminary efficacy, of a telephonic MBI for adults with SCD who have chronic pain. We will enroll 60 adult patients with SCD and chronic pain at an outpatient comprehensive SCD center in the southeastern United States. Patients will be randomized to either an MBI or a wait-listed control group. The MBI group will complete a six-session (60 minutes), telephonically delivered, group-based MBI program. The feasibility, acceptability, and efficacy of the MBI regarding pain catastrophizing will be assessed by administering questionnaires at baseline and weeks 1, 3, and 6. In addition, ten randomly selected MBI participants will complete semistructured interviews to help determine intervention acceptability. DISCUSSION: In this study protocol, we report detailed methods of the randomized controlled trial. Findings of this study will be useful to determine the acceptability, feasibility, and efficacy of an MBI for persons with SCD and chronic pain. TRIAL REGISTRATION: ClinicalTrials.gov identifier: NCT02394587 . Registered on 9 February 2015.