Pain, Chronic Clinical Trial
Official title:
Investigation Of The Effect Of Progressive Relaxation Training On Pain Characteristics, Attack Frequency, Perception Of Activity Self-Efficiency And Social Participation In Women With Tension-Type Headache And Migraine
Objective: The aim of this study was to investigate and compare the effects of PRT on pain characteristics, attack frequency, activity self-efficacy perception, and social participation in women with two different types of headaches, TTH and migraine. Methods: A total of 58 women within the age range of 20 to 45 were screened for eligibility in terms of suitability for participation in the study. Two separate progressive relaxation training sessions were administered to two distinct groups: one comprised of women with TTH and the other consisting of women with migraine. Pre- and post-training assessments were conducted for both groups as follows. Both intervention groups were instructed and trained by a physiotherapist 2times a week for 30 minutes each over 6 weeks,
Status | Recruiting |
Enrollment | 40 |
Est. completion date | July 10, 2024 |
Est. primary completion date | May 10, 2024 |
Accepts healthy volunteers | No |
Gender | Female |
Age group | 20 Years to 45 Years |
Eligibility | Inclusion Criteria: - the ages of 20 and 45, - having a diagnosis of TTH or migraine according to the International Classification of Headache Disorders (ICHD-II)(1), and - expressing voluntary willingness to participate in this study. Exclusion Criteria: - having any pathology involving the cervical region such as disc herniation, radiculopathy, a history of surgery, tumor, or cyst, - having received any form of physical therapy targeting the cervical region within the past 3 months, - being pregnant or in the menopausal phase; not participating in at least 15% of the training sessions, - having a mental disorder (being diagnosed with depression or using antidepressant medication), - having a chronic, neurological, or rheumatic disorder; suffering from sinusitis, and being on continuous prophylactic medication for migraines |
Country | Name | City | State |
---|---|---|---|
Turkey | Hacettepe University | Ankara |
Lead Sponsor | Collaborator |
---|---|
Hacettepe University |
Turkey,
Type | Measure | Description | Time frame | Safety issue |
---|---|---|---|---|
Primary | Occupational Self-Assessment (OSA): | OSA is a self-reported, client-centered evaluation tool based on MOHO, which assesses the degree of self-awareness and importance of the occupation by measuring the client's ability and value in performing routine occupation. It is a 4-point Likert-type scale consisting of 21 questions and 3 sections. | up to 5 months | |
Primary | World Health Organization Disability Assessment Schedule 2 (WHO-DAS II) | WHO-DAS II a 36-item general disability instrument that examines difficulties in six domains (activity limitations, communicating ,physical mobility, self-care participation in society, interpersonal interactions, domestic responsibilities and work of life during) in the last 30 days. Responses are given on a 5-point Likert-type scale from 1 (none) to 5 (extreme/cannot do). | up to 5 months | |
Primary | Pain Catastrophizing Scale (PCS): | The PCS is a 13-item questionnaire comprising three factors, rumination, magnification, and helplessness. Items are scored with a 5-point scale from 0 (not at all) to 4 (all the time). Total score ranges from 0 to 52 (27,28). High scores indicate a high level of catastrophizing. | up to 5 months | |
Primary | Headache Impact Test-6: | HIT-6, is a 6-item self-administered questionnaire. Items assess headache impact on lost time at work, school or social activities, pain severity, fatigue, frustration, and difficulty with concentration (21,22). Cut scores indicate the following categories: grade 1 (no effect if the scale score is =49), grade 2 (50-55 some impact), grade 3 (56-59 substantial impact), grade 4 (=60 as a severe impact). | up to 5 months | |
Primary | Visual Analog Scale (VAS): | Pain intensity was assessed with a 10-cm visual analogue scale (VAS). The VAS is scored on a 10- cm horizontal line with indicating 0 'no pain' and 10 'unbearable pain'. The women were asked to mark their headache pain on the horizontal line. (18). | up to 5 months | |
Secondary | Migraine Disability Assessment Scale (MIDAS): | MIDAS is a questionnaire designed to assess disability due to migraine in relation to work, household chores, and family, social or recreational activities over a three-month period (19,20). The MIDAS score is derived from responses reflecting the number of days missed due to headache and the occurrence of days with a 50% reduction in performance | up to 5 months |
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