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Effect of Mulligan Technique on Craniovertebral Angle in Females With Dowager's Hump (DH)

10 luglio 2026 aggiornato da: Nadia Abdelmoniem Abdelmeged, Cairo University
this study will be conducted to investigate the effect of Mulligan technique on craniovertebral angle, pain intensity, function neck disability, cervical range of motion, thoracic range of motion in females with dowager's hump.

Panoramica dello studio

Stato

Non ancora reclutamento

Condizioni

Intervento / Trattamento

Descrizione dettagliata

Dowager's hump is an abnormal outward curvature of the lower cervical and upper thoracic vertebrae in upper back which leads to the compression or wedging of the anterior portion of certain thoracic vertebrae. Hyperkyphosis is commonly reported in post- menopausal women due to associated osteoporosis. The curvature results in the forward bending of the spine (hyperkyphosis) and the formation of a hump at cervicothoracic junction and upper thoracic area . The Mulligan Technique is extensively applied in managing various cervical spine dysfunctions, particularly mechanical neck pain, cervicogenic headaches, and restricted cervical range of motion. Mobilizations with Movement (MWMs) targeting the cervical facet joints can effectively reduce pain and improve mobility in patients with neck stiffness and discomfort.Despite increasing interest in conservative treatment options, there remains a notable gap in the literature regarding the range and effectiveness of therapeutic approaches specifically targeting Dowager's hump. Most existing research has focused on general postural training or corrective exercises, with limited investigation into manual therapy techniques. To date, no studies have exclusively examined the use of the Mulligan concept as a treatment for Dowager's hump, even though it has demonstrated benefits in improving spinal alignment, joint mobility, and neuromuscular control in other musculoskeletal conditions.

Tipo di studio

Interventistico

Iscrizione (Stimato)

56

Fase

  • Non applicabile

Contatti e Sedi

Questa sezione fornisce i recapiti di coloro che conducono lo studio e informazioni su dove viene condotto lo studio.

Contatto studio

Criteri di partecipazione

I ricercatori cercano persone che corrispondano a una certa descrizione, chiamata criteri di ammissibilità. Alcuni esempi di questi criteri sono le condizioni generali di salute di una persona o trattamenti precedenti.

Criteri di ammissibilità

Età idonea allo studio

  • Adulto

Accetta volontari sani

No

Descrizione

Inclusion Criteria:

  • The age of patients will be ranged from 39 to 58 years old; mean menopausal age
  • The patients with CVA were less than 50°.
  • Pain intensity level will be examined by VAS which will be more than 3.
  • Limited cervical range of motion .
  • Limited thoracic range of motion (flexion, extension)
  • BMI will be more than 30 kg \m2.

Exclusion Criteria:

  • Patients with any neck surgeries.
  • Neurological infection and spinal cord injury.
  • Patients with congenital musculoskeletal deformities or ankylosing spondylitis.
  • Patients with cervical trauma or car accident.

Piano di studio

Questa sezione fornisce i dettagli del piano di studio, compreso il modo in cui lo studio è progettato e ciò che lo studio sta misurando.

Come è strutturato lo studio?

Dettagli di progettazione

  • Scopo principale: Trattamento
  • Assegnazione: Randomizzato
  • Modello interventistico: Assegnazione parallela
  • Mascheramento: Separare

Armi e interventi

Gruppo di partecipanti / Arm
Intervento / Trattamento
Sperimentale: Mulligan Technique
28 female patients will receive Mulligan technique for cervical & thoracic region and conventional treatment three times per week for four weeks
Altro: : Mulligan Technique
the patients will receive Mulligan technique in the form of Natural Apophyseal Glide (NAG) for cervical, Sustained natural apophysial glide ( SNAG ) for cervical,Sustained natural apophysial glide ( SNAG ) for Thoracic
Altro: conventional treatment.

The exercise program will consist of postural correction exercises to be performed under the supervision of a physical therapist. Each session will last 15-20 minutes per day, either under supervision or practiced individually at home. The exercises will include the following:

  • While seated, participants will lift both hands together above the head
  • While seated or standing with their back against a wall, participants will straighten their back as much as possible
  • While seated on a chair with both hands placed on the neck or crossed over the chest on the shoulders, participants will lift their arms and extend the upper back without compensating with hip or lumbar spine movement
  • While standing in front of a wall, participants will slide both hands upward along the wall as high as possible , Retraction in supine position,Retraction with extension,Pectoral stretch exercise training,Upper back extension exercise from prone training
Comparatore attivo: conventional treatment.
28 female patients will receive conventional treatment three times per week for four weeks
Altro: conventional treatment.

The exercise program will consist of postural correction exercises to be performed under the supervision of a physical therapist. Each session will last 15-20 minutes per day, either under supervision or practiced individually at home. The exercises will include the following:

  • While seated, participants will lift both hands together above the head
  • While seated or standing with their back against a wall, participants will straighten their back as much as possible
  • While seated on a chair with both hands placed on the neck or crossed over the chest on the shoulders, participants will lift their arms and extend the upper back without compensating with hip or lumbar spine movement
  • While standing in front of a wall, participants will slide both hands upward along the wall as high as possible , Retraction in supine position,Retraction with extension,Pectoral stretch exercise training,Upper back extension exercise from prone training

Cosa sta misurando lo studio?

Misure di risultato primarie

Misura del risultato
Misura Descrizione
Lasso di tempo
pain intensity
Lasso di tempo: up to four weeks
The patient will choose a number from the scale which represents value of pain intensity, VAS will be more than 3. Scores are based on self-reported measures of symptoms that are recorded with a single handwritten mark placed at one point along the length of a 10-cm line that represents a continuum between the two ends of the scale- "no pain" on the left end (0 cm) of the scale and the "worst pain" on the right end of the scale (10 cm).
up to four weeks
craniovertebral angle
Lasso di tempo: up to four weeks
The Craniovertebral Angle (CVA) was assessed using a standardized photographic method. Participants were instructed to stand or sit in a relaxed natural posture with the head maintained in a neutral position while facing forward. The spinous process of the seventh cervical vertebra (C7) and the tragus of the ear were identified by palpation and marked with adhesive markers to improve measurement accuracy. A lateral photograph was then captured using a digital camera positioned perpendicular to the participant's sagittal plane, approximately 1 m away at shoulder height. The image was analyzed using Kinovea software by drawing a horizontal line through the C7 marker and a second line connecting the C7 marker to the tragus. The angle formed between these two lines at C7 was recorded as the CVA. A smaller CVA indicates a greater degree of forward head posture, with values below 50° commonly considered indicative of forward head posture
up to four weeks

Misure di risultato secondarie

Misura del risultato
Misura Descrizione
Lasso di tempo
neck disability
Lasso di tempo: up to four weeks
neck disability index will be used to assess neck disability.The patient will set relaxed and asked to complete the neck disability index before treatment and after treatment. which consists of 10 items. Each item is scored from zero (no disability) to five (total disability), with the maximum possible total score being 50. For each item, the subject asked to choose one answer that best defined his/her neck functional disability level. Scores for each item tallied and the total score will recorded. Mean duration of the test: 3 to 7.8 minutes. Vernon and Mior presented the following interpretation.
up to four weeks
thoracic range of motion
Lasso di tempo: up to four weeks
Thoracic Schober test will be used to test thoracic range of motion by tape measurement. The tape measure is placed at the marked points, from the spinous process of T1 to the level of T12, and active flexion of the thoracic spine is requested. After completing the movement, the difference between the initial and final measurements (T1 and T12) is recorded as the Schober test flexion value of the thoracic spine. Normal mobility values are those that show a gain of at least 5 cm on the tape measure
up to four weeks
cervical range of motion
Lasso di tempo: up to four weeks
cervical range of motion will be measured by CROM device
up to four weeks

Collaboratori e investigatori

Qui è dove troverai le persone e le organizzazioni coinvolte in questo studio.

Sponsor

Cairo University

Studiare le date dei record

Queste date tengono traccia dell'avanzamento della registrazione dello studio e dell'invio dei risultati di sintesi a ClinicalTrials.gov. I record degli studi e i risultati riportati vengono esaminati dalla National Library of Medicine (NLM) per assicurarsi che soddisfino specifici standard di controllo della qualità prima di essere pubblicati sul sito Web pubblico.

Studia le date principali

Inizio studio (Stimato)

30 luglio 2026

Completamento primario (Stimato)

20 febbraio 2027

Completamento dello studio (Stimato)

20 febbraio 2027

Date di iscrizione allo studio

Primo inviato

10 luglio 2026

Primo inviato che soddisfa i criteri di controllo qualità

10 luglio 2026

Primo Inserito (Effettivo)

15 luglio 2026

Aggiornamenti dei record di studio

Ultimo aggiornamento pubblicato (Effettivo)

15 luglio 2026

Ultimo aggiornamento inviato che soddisfa i criteri QC

10 luglio 2026

Ultimo verificato

1 luglio 2026

Maggiori informazioni

Termini relativi a questo studio

Parole chiave

Altri numeri di identificazione dello studio

  • P.T.REC/012/006007

Informazioni su farmaci e dispositivi, documenti di studio

Studia un prodotto farmaceutico regolamentato dalla FDA degli Stati Uniti

No

Studia un dispositivo regolamentato dalla FDA degli Stati Uniti

No

Queste informazioni sono state recuperate direttamente dal sito web clinicaltrials.gov senza alcuna modifica. In caso di richieste di modifica, rimozione o aggiornamento dei dettagli dello studio, contattare register@clinicaltrials.gov. Non appena verrà implementata una modifica su clinicaltrials.gov, questa verrà aggiornata automaticamente anche sul nostro sito web .

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