Effektiviteten af Airrosti og TheraBand øvelser på dobbeltkrydset syndrom i smartphonebrugerens skulder ((Airrosti))
Effektiviteten af Airrosti og TheraBand øvelser mod smerter og handicap ved dobbeltkrydset syndrom i smartphonebrugerens skulder
Double-crossed syndrome" refers to a specific alignment of overactive and underactive muscles in the neck, chest, and shoulders. AIRROSTI stands for Applied Integration for the Rapid Recovery of Soft Tissue Injuries. This study aims to evaluate the effectiveness of Airrosti exercises combined with TheraBand exercises in reducing pain and disability in the neck and shoulders. TheraBand exercise programs are commonly used to improve muscle activation. However, research on the effectiveness of AIRROSTI combined with TheraBand exercises for treating Double-Crossed Syndrome among smartphone users is limited, and more evidence is needed to support their effectiveness.
Studieoversigt
Status
Betingelser
Intervention / Behandling
Detaljeret beskrivelse
Research objective is to evaluate the effectiveness of Airrosti and Theraband exercises in reducing pain and disability among smartphone users with Double-Crossed Syndrome. To evaluate the combined effect of Airrosti and Theraband exercises in reducing pain and disability among smartphone users with Double-Crossed Syndrome. To compare the effect of Airrosti and Theraband exercises in reducing pain and disability among smartphone users with Double-Crossed Syndrome.
Undersøgelsestype
Tilmelding (Faktiske)
Fase
- Ikke anvendelig
Kontakter og lokationer
Studiesteder
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Alriyadh
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Al Majma'ah, Alriyadh, Saudi Arabien, 11952
- Majmaah University
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Deltagelseskriterier
Berettigelseskriterier
Aldre berettiget til at studere
Tager imod sunde frivillige
Køn, der er berettiget til at studere
Beskrivelse
Inclusion Criteria:
young female participants with rounded shoulder postures. Participants aged between 18 and 25 years. No history of shoulder trauma, current shoulder pathology, thoracic scoliosis, and kyphosis deformity.
Exclusion Criteria:
Participants excluded if they received any other form of medical treatment or have thoracic scoliosis or kyphosis deformity.
Studieplan
Hvordan er undersøgelsen tilrettelagt?
Design detaljer
- Primært formål: Behandling
- Tildeling: Randomiseret
- Interventionel model: Parallel tildeling
- Maskning: Enkelt
Våben og indgreb
Deltagergruppe / Arm |
Intervention / Behandling |
|---|---|
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Aktiv komparator: Groupe A
Experimental groupe A will receive AIRROSTI exercises for 45 minutes / one session daily for five days per week. |
Group A will receive AIRROSTI exercises for 45 minutes / one session daily for five days per week |
|
Aktiv komparator: Groupe B
Group B will receive Thera band exercises for 45 minutes/one session per day for five days per week. |
Group B will receive Thera band exercises for 45 minutes/one session per day for five days per week. |
Hvad måler undersøgelsen?
Primære resultatmål
Resultatmål |
Foranstaltningsbeskrivelse |
Tidsramme |
|---|---|---|
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University of California at Los Angeles Activity Scale
Tidsramme: 6 week
|
Pre and post intervention measurement will be taken using University of California at Los Angeles Activity Scale. The minimum score is zero indicating several functional impairments and maximum score is 35 , indicating a normal upper limb activity. |
6 week
|
Andre resultatmål
Resultatmål |
Foranstaltningsbeskrivelse |
Tidsramme |
|---|---|---|
|
Double Square Test
Tidsramme: 6week
|
Pre and post intervention measurement will be taken on Double Square Test.The minimum score is 0, and the maximum score is 10, corresponding to severe disability and optimal function, respectively. |
6week
|
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Numeric Pain rating scale
Tidsramme: 6 week
|
Pre and post intervention measurement will be taken on Numeric Pain rating scale. The minimum score is 0, indicating no pain, and maximum score is 10 , indicating worst pain imaginable. |
6 week
|
Samarbejdspartnere og efterforskere
Sponsor
Efterforskere
- Ledende efterforsker: Shahnaz Hasan associate Professor, PhD, Majmaah University
Datoer for undersøgelser
Studer store datoer
Studiestart (Faktiske)
Primær færdiggørelse (Faktiske)
Studieafslutning (Faktiske)
Datoer for studieregistrering
Først indsendt
Først indsendt, der opfyldte QC-kriterier
Først opslået (Faktiske)
Opdateringer af undersøgelsesjournaler
Sidste opdatering sendt (Faktiske)
Sidste opdatering indsendt, der opfyldte kvalitetskontrolkriterier
Sidst verificeret
Mere information
Begreber relateret til denne undersøgelse
Andre undersøgelses-id-numre
- MUREC-Oct.03/COM-2024/48
Plan for individuelle deltagerdata (IPD)
Planlægger du at dele individuelle deltagerdata (IPD)?
IPD-planbeskrivelse
There is no plan to share, it will be available with principal author and provided upon request.
Lægemiddel- og udstyrsoplysninger, undersøgelsesdokumenter
Studerer et amerikansk FDA-reguleret lægemiddelprodukt
Studerer et amerikansk FDA-reguleret enhedsprodukt
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