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Yoga, Mindfulness and Cognitive Psychotherapy as Treatment for Stress and Burnout

Yoga, Mindfulness and Cognitive Psychotherapy as Treatment for Stress and Burnout

Status
Completed
Phases
NA
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT01168661
Enrollment
90
Registered
2010-07-23
Start date
2007-08-31
Completion date
2010-04-30
Last updated
2010-07-23

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Anxiety, Burnout, Professional, Depression, Stress, Psychological

Keywords

Stress, Burnout, Anxiety, Depression

Brief summary

The purpose of this study is to investigate if treatment with yoga or mindfulness has a more profound and longstanding effect on stress and burnout than treatment with cognitive psychotherapy alone.

Interventions

BEHAVIORALYoga

Participants in this intervention arm will practice yoga (physical postures, breathing exercises, and meditation) \>= 5 times a week (twice in a supervised group and the rest on their own). Additionally, participants in this arm will practice various practical skills, such as how to plan a satisfactory day using their own definition of a satisfactory day. They will follow this schedule for 20 weeks.

BEHAVIORALMindfulness based cog psychotherapy

Participants in this arm will attend a weekly group meeting to practice mindfulness based cognitive psychotherapy. They will also practice \>= 4 time a week on their own. Additionally, participants in this arm will practice various practical skills, such as how to plan a satisfactory day using their own definition of a satisfactory day. Participants will follow this schedule for 20 weeks.

BEHAVIORALCognitive psychotherapy

Participants in this arm will attend a weekly group meeting to practice cognitive psychotherapy. They will also practice \>= 4 time a week on their own. Additionally, participants in this arm will practice various practical skills, such as how to plan a satisfactory day using their own definition of a satisfactory day. Participants will follow this schedule for 20 weeks.

Sponsors

Region Stockholm
CollaboratorOTHER_GOV
Karolinska Institutet
Lead SponsorOTHER

Study design

Allocation
RANDOMIZED
Intervention model
PARALLEL
Primary purpose
TREATMENT
Masking
NONE

Eligibility

Sex/Gender
ALL
Age
16 Years to 65 Years
Healthy volunteers
No

Inclusion criteria

* On sick leave at least 50% at the beginning of the study. * Sick leave for a maximum of 1 year if on full-time sick leave at the beginning of the study or for a maximum of 3 years if on part-time sick leave at the beginning of the study. * Speak Swedish well enough to participate in the study interventions. * Body mass index (BMI) of between 18 and 30. * Meet the diagnostic criteria for burnout syndrome from the Swedish National Board of Health and Welfare.

Exclusion criteria

* Medication, including all medication or topical skin preparations with cortisone in any form. Exceptions: Antidepressants, contraceptives, hormone replacement therapy for hypothyroidism if hormone levels were within the normal range, and hormone replacement therapy to treat menopausal symptoms. To receive an exception for medication, a participant had to take the same medication at the same dose at both blood tests.

Design outcomes

Primary

MeasureTime frameDescription
Reduced stress measured by qualitative questionnaires5 months after start of treatmentLevel of stress will be measured by qualitiative questionnaries, including the Swedish Health-Related Quality of Life Survey (SWEQUAL).

Secondary

MeasureTime frameDescription
Reduced cortisol secretion5 months after start of treatmentWe will measure cortisol level in a 24-hour sample of urine.

Countries

Sweden

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Mar 7, 2026