The Effect of Two Different Massages on Migraine

NCT ID: NCT05452330

Last Updated: 2022-09-21

Study Results

Results pending

The study team has not published outcome measurements, participant flow, or safety data for this trial yet. Check back later for updates.

Basic Information

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Recruitment Status

COMPLETED

Clinical Phase

NA

Total Enrollment

30 participants

Study Classification

INTERVENTIONAL

Study Start Date

2022-07-18

Study Completion Date

2022-09-16

Brief Summary

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The study aims to compare the effects of connective tissue massage on pain severity, attack frequency and duration, migraine-related disability, and quality of life in patients diagnosed with migraine, by comparing them with the classical massage.

Detailed Description

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Conditions

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Headache, Migraine Manuel Therapy

Study Design

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Allocation Method

RANDOMIZED

Intervention Model

PARALLEL

Primary Study Purpose

TREATMENT

Blinding Strategy

SINGLE

Outcome Assessors

Study Groups

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Group 1

Connective tissue massage

Group Type EXPERIMENTAL

Connective tissue massage

Intervention Type OTHER

Connective tissue massage will be applied with short and long pulling strokes to create a reflex effect for 2 days a week, a total of 8 weeks.

Group 2

Classical massage

Group Type EXPERIMENTAL

Classical massage

Intervention Type OTHER

Classical massage will be applied with the techniques of stroking, kneading, and friction for 2 days a week, a total of 8 weeks.

Interventions

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Connective tissue massage

Connective tissue massage will be applied with short and long pulling strokes to create a reflex effect for 2 days a week, a total of 8 weeks.

Intervention Type OTHER

Classical massage

Classical massage will be applied with the techniques of stroking, kneading, and friction for 2 days a week, a total of 8 weeks.

Intervention Type OTHER

Eligibility Criteria

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Inclusion Criteria

* Volunteers with a migraine diagnosis
* Taking only analgesics for migraine treatment and continuing their routines
* No problem in reading, writing and understanding Turkish

Exclusion Criteria

* Having any other neurological problems
* Who had been injected with botulinum toxin in the last 3 months
Minimum Eligible Age

18 Years

Maximum Eligible Age

64 Years

Eligible Sex

ALL

Accepts Healthy Volunteers

No

Sponsors

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Biruni University

OTHER

Sponsor Role lead

Responsible Party

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Begum Kara Kaya

Clinical investigator

Responsibility Role PRINCIPAL_INVESTIGATOR

Principal Investigators

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Arzu Özdinçler, PhD

Role: STUDY_CHAIR

Biruni University

Locations

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Biruni University

Istanbul, Zeytinburnu, Turkey (Türkiye)

Site Status

Countries

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Turkey (Türkiye)

Other Identifiers

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Migren

Identifier Type: -

Identifier Source: org_study_id

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