Tension-Type Headache Clinical Trial
Official title:
Yoga and Mindfulnes-based-stress-reduction for Patients With Tension-type Headache
Primary study objectives 1. evaluate the short-term effect of yoga intervention in addition to routine care on headache frequency in patients with frequent or chronic tension-type headache compared to routine care alone (waiting group). 2. to evaluate the short-term effect of yoga intervention in addition to routine care on headache frequency in patients with frequent episodic or chronic tension-type headache compared with stress management through mindfulness-based stress reduction (MBSR) in addition to routine care. Secondary study objectives Evaluation of the medium-term effect of the intervention on headache frequency as well as the short- and medium-term effect on the secondary target parameters in comparison to the waiting group and MBSR. Further evaluation of the safety and acceptability of the intervention.
Status | Recruiting |
Enrollment | 72 |
Est. completion date | December 30, 2021 |
Est. primary completion date | July 1, 2021 |
Accepts healthy volunteers | No |
Gender | All |
Age group | 18 Years to 65 Years |
Eligibility | Inclusion Criteria: - episodic or chronic tension-type headache according to ICHD-3 definition Exclusion Criteria: - medication induced headache according to ICHD-3 definition - Cluster-headache according to ICHD-3 definition - serious chronic systemic or acute physical or mental illness - Dementia - Pregnancy - actual in a yoga or MBSR class |
Country | Name | City | State |
---|---|---|---|
Germany | Evang. Kliniken Essen-Mitte | Essen | Northrhine-Westphalia |
Lead Sponsor | Collaborator |
---|---|
Universität Duisburg-Essen | Eden Stiftung |
Germany,
Type | Measure | Description | Time frame | Safety issue |
---|---|---|---|---|
Primary | Headache Frequency | Headache Frequency self-reported by a headache diary | post-intervention (8 weeks) | |
Secondary | Headache Frequency | Headache Frequency self-reported by a headache diary | follow-up (20 weeks) | |
Secondary | Duration of headache episodes | Duration of headache episodes self-reported by a headache diary | post-intervention (8 weeks) | |
Secondary | Duration of headache episodes | Duration of headache episodes self-reported by a headache diary | follow-up (20 weeks) | |
Secondary | Pain Intensity | Numeric rating scale | post-intervention (8 weeks) | |
Secondary | Pain Intensity | Numeric rating scale (NRS) | follow-up (20 weeks) | |
Secondary | Pain medication use | Pain medication use self-reported by a headache diary | post-intervention (8 weeks) | |
Secondary | Pain medication use | Pain medication use self-reported by a headache diary | follow-up (20 weeks) | |
Secondary | Headache related disability | Headche Impact Test 6 (HIT-6) | post-intervention (8 weeks) | |
Secondary | Headache related disability | Headche Impact Test 6 (HIT-6) | follow-up (20 weeks) | |
Secondary | Health-related quality of life | SF-36 questionaire | post-intervention (8 weeks) | |
Secondary | Health-related quality of life | SF-36 questionaire | follow-up (20 weeks) | |
Secondary | Anxiety | Depression and Anxiety scale (DAAS) | post-intervention (8 weeks) | |
Secondary | Anxiety | Depression and Anxiety scale (DAAS) | follow-up (20 weeks) | |
Secondary | Stress | Depression and Anxiety scale (DAAS) | post-intervention (8 weeks) | |
Secondary | Stress | Depression and Anxiety scale (DAAS) | follow-up (20 weeks) | |
Secondary | Pain catastrophizing | Pain catastrophizing scale (PCS) | post-intervention (8 weeks) | |
Secondary | Pain catastrophizing | Pain catastrophizing scale (PCS) | follow-up (20 weeks) | |
Secondary | Pain acceptance | Chronic pain acceptance questionaire (CPAQ) | post-intervention (8 weeks) | |
Secondary | Pain acceptance | Chronic pain acceptance questionaire (CPAQ) | follow-up (20 weeks) | |
Secondary | Mindfulness | Mindfulness Attention and Awerness scale (MAAS) | post-intervention (8 weeks) | |
Secondary | Mindfulness | Mindfulness Attention and Awerness scale (MAAS) | follow-up (20 weeks) | |
Secondary | Body Awareness | Body Awareness questionaire (BAQ) | post-intervention (8 weeks) | |
Secondary | Body Awareness | Body Awareness questionaire (BAQ) | follow-up (20 weeks) | |
Secondary | Safety | Adverse events | post-intervention (8 weeks) | |
Secondary | Safety | Adverse events | follow-up (20 weeks) |
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