- ICH GCP
- Amerikanska kliniska prövningsregistret
- Klinisk prövning NCT07628413
Comparative Effects of Egoscue and Feldenkrais Exercises on in Upper Cross Syndrome
Comparative Effects of Egoscue and Feldenkrais Exercises on Pain, Craniovertebral Angle and Functional Disability in Upper Cross Syndrome
Upper cross syndrome is a common postural dysfunction that is caused due to alternating tightness and weakness in the opposite muscle groups of the neck, shoulders and upper back which results in abnormal postural deviations. The aim of the study will be to compare the effects of Egoscue exercises and Feldenkrais exercises on pain, craniovertebral angle and functional disability in upper cross syndrome.
A Randomized clinical trial will be conducted at Ghurki Trust Teaching Hospital, Lahore and Riphah clinic, Lahore through non probability convenience sampling technique on 54 patients which will be allocated using simple random sampling through sealed opaque envelop into Group A and Group B. Group A will be treated with Egoscue exercises and conventional therapy and Group B will be treated with Feldenkrais exercises and conventional therapy at the frequency of 3 sets with 10 repetitions thrice a week. Outcome measures will be conducted through pain, craniovertebral angle and functional disability after 4 weeks. Data will be analyzed with SPSS software version 26. After assessing the normality of data by Shapiro-Wilk test, it will be decided either parametric or non- parametric will be used within the group or between the groups.
Studieöversikt
Status
Betingelser
Intervention / Behandling
Studietyp
Inskrivning (Beräknad)
Fas
- Inte tillämpbar
Kontakter och platser
Studiekontakt
- Namn: iqbal Tariq, phd
- Telefonnummer: 03338236752
- E-post: iqbal.tariq@riphah.edu.pk
Studera Kontakt Backup
- Namn: Rabiya Noor, phd
- Telefonnummer: 03344355660
- E-post: Rabiya.Noor@riphah.edu.pk
Studieorter
-
-
Punjab Province
-
Lahore, Punjab Province, Pakistan, 54000
- Rekrytering
- Rabiya Noor
-
-
Deltagandekriterier
Urvalskriterier
Åldrar som är berättigade till studier
- Vuxen
Tar emot friska volontärer
Beskrivning
Inclusion Criteria:
- Age 25 to 45 years
- Both genders (male and female)
- Chronic neck pain for more than three months - NPRS (3 to 7)
- Craniovertebral angle less than 50 degrees
- Tight Pectoralis muscle and trapezius
- Weak rhomboids and deep neck flexors
Exclusion Criteria:
- Any malignancy related to soft tissue and shoulder joint
- Congenital joint deformity
- Recent fractures to joint
- Recent surgery of shoulder joint or associated structures
- Patients with shoulder dislocation
Studieplan
Hur är studien utformad?
Designdetaljer
- Primärt syfte: Behandling
- Tilldelning: Randomiserad
- Interventionsmodell: Parallellt uppdrag
- Maskning: Enda
Vapen och interventioner
Deltagargrupp / Arm |
Intervention / Behandling |
|---|---|
|
Experimentell: Egoscue exercises
|
|
|
Aktiv komparator: Feldenkrais exercises
|
|
Vad mäter studien?
Primära resultatmått
Resultatmått |
Åtgärdsbeskrivning |
Tidsram |
|---|---|---|
|
Disability Index (DNI)
Tidsram: 6th week
|
This questionnaire will be used to asses disability.
It comprises of 10 items; 7 related to daily living activities; 2 related to pain and 1 related to concentration.
Each item is scored from 0 to 5. Total score is expressed as a percentage, with higher scores related to greater disability.
Minimum detectable change measurements vary from 4.2 to 13.4, and minimum clinically important differences vary from 5 and 9.5
|
6th week
|
|
Craniovertebral angle (CVA)
Tidsram: 6th week
|
Craniovertebral angle can be measured with Image J software.
If the angle is less than 50 degrees (< 50 degree).
The angle will be between tragus of the ear to cervical spinous process C7.
|
6th week
|
Samarbetspartners och utredare
Sponsor
Utredare
- Huvudutredare: areesha shakeel, MSPT(CP), Riphah International University
Publikationer och användbara länkar
Studieavstämningsdatum
Studera stora datum
Studiestart (Faktisk)
Primärt slutförande (Beräknad)
Avslutad studie (Beräknad)
Studieregistreringsdatum
Först inskickad
Först inskickad som uppfyllde QC-kriterierna
Första postat (Faktisk)
Uppdateringar av studier
Senaste uppdatering publicerad (Faktisk)
Senaste inskickade uppdateringen som uppfyllde QC-kriterierna
Senast verifierad
Mer information
Termer relaterade till denna studie
Nyckelord
Ytterligare relevanta MeSH-villkor
Andra studie-ID-nummer
- REC/RCR&AHS/25/0111
Plan för individuella deltagardata (IPD)
Planerar du att dela individuella deltagardata (IPD)?
Läkemedels- och apparatinformation, studiedokument
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