Mandala Coloring for Pain, Fatigue, and Sleep in Patients With Fibromyalgia
The Effect of Mandala Coloring on Pain, Fatigue, and Sleep Quality in Patients With Fibromyalgia
Fibromyalgia is a chronic condition commonly associated with widespread pain, fatigue, and poor sleep quality. This randomized controlled study aims to determine whether mandala coloring, when added to routine treatment, improves pain, fatigue, and sleep quality in adults with fibromyalgia.
A total of 60 eligible participants will be randomly assigned in a 1:1 ratio to either a mandala coloring group or a control group. Participants in the mandala coloring group will complete eight 60-minute coloring sessions over four weeks, with two sessions per week, while continuing their routine treatment. Participants in the control group will continue their routine treatment without taking part in a structured coloring activity.
Pain, fatigue, and sleep quality will be assessed at the beginning of the study and at the end of the fourth week. Changes in these outcomes will be compared between the two groups.
Studienübersicht
Status
Bedingungen
Intervention / Behandlung
Detaillierte Beschreibung
This is a single-center, two-arm, parallel-group randomized controlled trial designed to evaluate the effects of mandala coloring on pain, fatigue, and sleep quality in adults with fibromyalgia. The study will be conducted in the Physical Medicine and Rehabilitation Outpatient Clinic of Artvin State Hospital.
Sixty participants who meet the eligibility criteria will be enrolled. Following the baseline assessment, participants will be randomly assigned in a 1:1 ratio to the mandala coloring group or the control group using a simple randomization method.
Participants assigned to the intervention group will receive colored pencils and a coloring booklet containing mandala patterns. They will complete eight supervised mandala coloring sessions over four weeks. The sessions will be conducted twice weekly, and each session will last approximately 60 minutes. Participants will continue receiving their routine treatment throughout the study.
Participants assigned to the control group will continue their routine treatment and will not participate in any structured mandala coloring activity during the four-week study period.
Outcome assessments will be performed at baseline and at the end of week 4. Pain intensity will be assessed using the Visual Analog Scale for Pain, fatigue will be assessed using the Fatigue Severity Scale, and sleep quality will be assessed using the Pittsburgh Sleep Quality Index. Changes in outcome scores will be compared within and between the study groups.
Studientyp
Einschreibung (Geschätzt)
Phase
- Unzutreffend
Kontakte und Standorte
Studienorte
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Artvin, Schweiz
- Artvin State Hospital
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Kontakt:
- Emre ERKAL, PhD
- Telefonnummer: 5433750709
- E-Mail: emre.erkal@artvin.edu.tr
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Teilnahmekriterien
Zulassungskriterien
Studienberechtigtes Alter
- Erwachsene
- Älterer Erwachsener
Akzeptiert gesunde Freiwillige
Beschreibung
Inclusion Criteria:
- Aged 18 years or older
- Diagnosed with fibromyalgia
- Pain intensity score of 5 or higher on the Visual Analog Scale
- Fatigue Severity Scale score of 4 or higher
- Pittsburgh Sleep Quality Index global score of 5 or higher
- Able to communicate and complete the study assessments
- No physical limitation preventing mandala coloring
- Willing to participate and provide written informed consent
Exclusion Criteria:
- Presence of a communication problem that prevents participation or completion of the assessments
- Presence of a physical limitation that prevents mandala coloring
- Refusal to participate or provide written informed consent
Studienplan
Wie ist die Studie aufgebaut?
Designdetails
- Hauptzweck: Unterstützende Pflege
- Zuteilung: Zufällig
- Interventionsmodell: Parallele Zuordnung
- Maskierung: Keine (Offenes Etikett)
Waffen und Interventionen
Teilnehmergruppe / Arm |
Intervention / Behandlung |
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Experimental: Mandala Coloring Group
Participants will complete eight supervised mandala coloring sessions over four weeks, with two 60-minute sessions per week.
Colored pencils and a coloring booklet containing mandala patterns will be provided.
Participants will continue receiving their routine treatment throughout the study.
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Participants will complete eight supervised mandala coloring sessions over four weeks.
Sessions will be conducted twice weekly, and each session will last 60 minutes.
Participants will use colored pencils and a coloring booklet containing mandala patterns while continuing their routine treatment.
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Kein Eingriff: Control Group
Participants will continue receiving their routine treatment for four weeks and will not participate in any structured mandala coloring activity during the study period.
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Was misst die Studie?
Primäre Ergebnismessungen
Ergebnis Maßnahme |
Maßnahmenbeschreibung |
Zeitfenster |
|---|---|---|
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Change From Baseline in Pain Intensity Assessed by the Visual Analog Scale at Week 4
Zeitfenster: Baseline and end of week 4
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Pain intensity will be assessed using a 10-cm Visual Analog Scale, ranging from 0 (no pain) to 10 (worst imaginable pain).
Higher scores indicate greater pain intensity.
The outcome will be evaluated as the change in the Visual Analog Scale score from baseline to the end of week 4.
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Baseline and end of week 4
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Sekundäre Ergebnismessungen
Ergebnis Maßnahme |
Maßnahmenbeschreibung |
Zeitfenster |
|---|---|---|
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Change From Baseline in Fatigue Severity Assessed by the Fatigue Severity Scale at Week 4
Zeitfenster: Baseline and end of week 4
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Fatigue will be assessed using the nine-item Fatigue Severity Scale.
Each item is scored from 1 (strongly disagree) to 7 (strongly agree), and the total score is calculated as the mean of the nine items.
Scores range from 1 to 7, with higher scores indic
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Baseline and end of week 4
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Change From Baseline in Sleep Quality Assessed by the Pittsburgh Sleep Quality Index at Week 4
Zeitfenster: Baseline and end of week 4
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Sleep quality will be assessed using the Pittsburgh Sleep Quality Index.
The global score ranges from 0 to 21, with higher scores indicating poorer sleep quality.
A global score of 5 or higher indicates poor sleep quality.
The outcome will be evaluated as the change in the global score from baseline to the end of week 4.
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Baseline and end of week 4
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Mitarbeiter und Ermittler
Sponsor
Studienaufzeichnungsdaten
Haupttermine studieren
Studienbeginn (Geschätzt)
Primärer Abschluss (Geschätzt)
Studienabschluss (Geschätzt)
Studienanmeldedaten
Zuerst eingereicht
Zuerst eingereicht, das die QC-Kriterien erfüllt hat
Zuerst gepostet (Tatsächlich)
Studienaufzeichnungsaktualisierungen
Letztes Update gepostet (Tatsächlich)
Letztes eingereichtes Update, das die QC-Kriterien erfüllt
Zuletzt verifiziert
Mehr Informationen
Begriffe im Zusammenhang mit dieser Studie
Zusätzliche relevante MeSH-Bedingungen
Andere Studien-ID-Nummern
- ACU-FM-MANDALA-2026
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Studiert ein von der US-amerikanischen FDA reguliertes Arzneimittelprodukt
Studiert ein von der US-amerikanischen FDA reguliertes Geräteprodukt
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