Table 3.
NCT Identifier and/or Author | Study Design | Intervention | Primary Outcome Measurement Tool |
---|---|---|---|
NCT04868357 | Trial: HYPNOBPCO_2; 2-arm, cluster-randomized, statistician-blinded superiority monocenter trial, 100 participants with Hypnosis” (treatment) and “Relaxation” (active control). “Hypnosis” will consist Pulmonary Rehabilitation Program, supplemented by two educational sessions for teaching self-hypnosis. Relaxation group will be identical, except standard relaxation exercises will be taught instead of hypnosis. |
Hypnosis as a tool to manage anxiety and dyspnea post pulmonary rehabilitation program (PRP). | State-Trait Anxiety Inventory (STAI-6) Hospital Anxiety and Depression inventory (HADS) Multidimensional Dyspnea Profile (MDP) |
NCT05506202 | Randomized clinical trial; n = 36 | Treatment group: Basic body awareness therapy Control group: basic and advanced respiratory physiotherapy interventions |
Modified Medical Research Council scale for breathlessness Dyspnoea-12 (Chinese version) St. George’s Respiratory Questionnaire (Chinese version) COPD Self-Efficacy Scale (CSES) (Chinese version) 6 min walking test |
NCT04860375 | Prospective, open label, cohort study; n = 110 | Treatment group: Multidisciplinary patient care (dietary program, adjusted exercise program, psychological counseling, treatment of comorbidities) Control group: Standard care |
Total number of hospitalizations |
NCT04898972 | Randomized clinical trial; n = 80 | Mindfulness-based stress reduction (body scan; sitting meditation; awareness movement exercises; and walking meditation) Control group: informative booklet on stress reduction strategies |
Perceived Stress Scale (PSS) Generalized Anxiety Disorder scale (GAD-7) Patient Health Questionnaire (PHQ-9) |