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Clinical Trials/NCT03888261
NCT03888261
Unknown
N/A

Effectiveness of Mind-Body Approaches for Three Distinct Medical Conditions: A Pragmatic Randomized Controlled Television Broadcast Experiment

University Hospital, Gentofte, Copenhagen0 sites90 target enrollmentApril 1, 2019

Overview

Phase
N/A
Intervention
Not specified
Conditions
Rheumatoid Arthritis
Sponsor
University Hospital, Gentofte, Copenhagen
Enrollment
90
Primary Endpoint
WHO-Five Well-being Index
Last Updated
7 years ago

Overview

Brief Summary

Chronic diseases are currently the most prevalent and most costly health conditions world-wide, and morbidity is expected to increase over coming years. Factors such that increased life-expectancy and certain life style-related factors, such as smoking, high-fat diet and alcohol-consumption, are commonly associated with the increase in most of the common chronic diseases. However, more complex psychosocial factors such as depression, stress, work-related dynamics and thinking patterns are thought be associated with poor health status and impaired health related quality of life among patients with suffering from chronic physical conditions (i.e. a biopsychosocial approach). Therefore, psychosocial intervention has been suggested as a complementary treatment strategy for patients with chronic conditions.

The aim of this randomized trial is to evaluate the effectiveness of mind-body multidisciplinary rehabilitation on health-related quality of life, and disease specific endpoints in people with rheumatoid arthritis, psoriasis, or heart failure.

Registry
clinicaltrials.gov
Start Date
April 1, 2019
End Date
January 1, 2020
Last Updated
7 years ago
Study Type
Interventional
Study Design
Parallel
Sex
All

Investigators

Sponsor
University Hospital, Gentofte, Copenhagen
Responsible Party
Principal Investigator
Principal Investigator

Lina R. Khoury

Post-doctoral Researcher

University Hospital, Gentofte, Copenhagen

Eligibility Criteria

Inclusion Criteria

  • Rheumatoid arthritis:
  • RA according to the 1987 revised American College of Rheumatology criteria
  • Not selected on the basis of their level of activity.
  • The treatment of both the RA and any other medical condition have to be stable and constant for at least three months at the time of enrolment, and no future planned changes of therapy exist at the time of inclusion.
  • Oral corticosteroids, if used previously, will be allowed at a maximum prednisone dose with an equivalent of 10mg/day.
  • Diagnosed plaque psoriasis for 6 months or longer
  • Psoriasis medical condition have to be stable and constant for at least three months at the time of enrolment (i.e. no future planned changes of therapy exist at the time of inclusion).
  • Exclusion criteria are other immune-mediated conditions requiring current systemic immunosuppressant treatment except psoriatic arthritis.
  • Heart Failure with reduced ejection fraction:
  • Symptomatic patients (NYHA class II or III, or NYHA class IV if CRT planned at enrolment) with systolic heart failure (left ventricular ejection fraction ≤40%) will be considered eligible for enrolment.

Exclusion Criteria

  • Ability to participate
  • Psychopathology: Persons with severe mental illness are excluded.
  • Alcohol and/ or drug abuse
  • Impaired cognitive functions

Outcomes

Primary Outcomes

WHO-Five Well-being Index

Time Frame: At baseline, 10-12 weeks (1-2 weeks post-intervention), and 26 weeks from baseline

All participants. The WHO-5 consists of five statements. The total raw score, ranging from 0 to 25, is multiplied by 4 to give the final score, with 0 representing the worst imaginable well-being and 100 representing the best imaginable well-being.

Secondary Outcomes

  • Hospital anxiety and depression scale (HADS)(At baseline, 10-12 weeks (1-2 weeks post-intervention), and 26 weeks from baseline)
  • SF36: Physical Component Summary (PCS)(At baseline, 10-12 weeks (1-2 weeks post-intervention), and 26 weeks from baseline)
  • Illness Perception Questionnaire(At baseline, 10-12 weeks (1-2 weeks post-intervention), and 26 weeks from baseline)
  • Mindful Attention Awareness Scale-5(At baseline, 10-12 weeks (1-2 weeks post-intervention), and 26 weeks from baseline)
  • High-sensitivity C-reactive protein (hs-CRP)(At baseline, 10-12 weeks (1-2 weeks post-intervention), and 26 weeks from baseline)
  • Cohen's Perceived Stress Scale(At baseline, 10-12 weeks (1-2 weeks post-intervention), and 26 weeks from baseline)
  • SF36: Mental Component Summary (MCS)(At baseline, 10-12 weeks (1-2 weeks post-intervention), and 26 weeks from baseline)
  • Pittsburgh sleep quality index(At baseline, 10-12 weeks (1-2 weeks post-intervention), and 26 weeks from baseline)
  • Self-Compassion Scale(At baseline, 10-12 weeks (1-2 weeks post-intervention), and 26 weeks from baseline)

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