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Rehabilitation Outcomes in Head and Neck Survivors

Vain rekisteröityneet käyttäjät voivat kääntää artikkeleita
Kirjaudu sisään Rekisteröidy
Linkki tallennetaan leikepöydälle
TilaValmistunut
Sponsorit
Chang Gung Memorial Hospital

Avainsanat

Abstrakti

Head and neck cancer is prevalent in Taiwan, and oral cancer is the most common location. Patients with advanced stage of the disease need extensive tumor excision with neck dissection. Secondary reconstructive surgeries using free flap could improve the postoperative function or appearance of cancer survivors. Advanced treatments make survival rates increased. Effects of treatment for oral cancer develop shoulder dysfunction, speech, mastication, donor site morbidity and psychological issues. Physical therapy may have benefits for temporomandibular joint function, shoulder pain relief, muscle performance, and oral structures coordination. Return to work in the number of cancer survivors is a realistic outcome. Rehabilitation effects on functional restorations and quality of life for head and neck survivors are needed for further studied.
The purpose of this project is to explore the rehabilitation effects following head and neck reconstructive survivors. The investigators measure temporomandibular joint function, shoulder function, pain monthly. Physical functions, self-reported quality of life, and the status of return to work are measured 3 and 6 months after surgery. This prospective study could help to predict the rehabilitation outcomes and benefits.

Kuvaus

Head and neck cancer is prevalent in Taiwan, and oral cancer is the most common location. Patients with advanced stage of the disease need extensive tumor excision with neck dissection. Secondary reconstructive surgeries using free flap could improve the postoperative function or appearance of cancer survivors. Oral functions include respiration, speech, mastication, deglutition, and cosmetics. Advanced treatments make survival rates increased, but might develop shoulder dysfunction, speech, mastication, donor site morbidity and psychological issues. The purpose of this project is to explore the effects of rehabilitation following reconstructive surgery in oral cancer survivors.

This study design is an interrupted time-series design. The investigators will recruit 50 subjects one week following reconstructive surgery. The measurements include manual muscle strength, joint range of motion, maximal mouth opening, pain status, hand-to-neck test, hand-to-scapula test, hand-to-opposite-scapula test, 6-minute walking test, timed up & go test, European Organization for Research and Treatment of Cancer (EORTC) quality of life questionnaire (QLQ)-C30, European Organization for Research and Treatment of Cancer (EORTC) quality of life questionnaire (QLQ)-H&N35 and return-to-work. These tests were done at the first visit (0 week post-operation), three months and six months after reconstructive surgery respectively. The intervention programs consist of edema control, scar management, pain management, respiration training, oral function training, neck and shoulder function training, donor site mobility training. Continuous variables were analyzed by descriptive statistics. One-way ANOVA was used to compare the difference between measurements. Binary logistic regression was used to predict the factors of return-to-work.

Päivämäärät

Viimeksi vahvistettu: 04/30/2015
Ensimmäinen lähetys: 02/16/2015
Arvioitu ilmoittautuminen lähetetty: 06/29/2017
Ensimmäinen lähetetty: 07/01/2017
Viimeisin päivitys lähetetty: 06/29/2017
Viimeisin päivitys lähetetty: 07/01/2017
Todellinen opintojen alkamispäivä: 12/31/2014
Arvioitu ensisijainen valmistumispäivä: 06/29/2016
Arvioitu tutkimuksen valmistumispäivä: 06/29/2016

Ehto tai tauti

Head and Neck Cancer
Oral Cancer

Interventio / hoito

Other: Physiotherapy

Vaihe

-

Varren ryhmät

VarsiInterventio / hoito
initial
0 month begin physiotherapy
3 months after physiotherapy
3 months after physiotherapy
6 months after physiotherapy
6 months after physiotherapy

Kelpoisuusehdot

Tutkimukseen soveltuvat iät 20 Years Vastaanottaja 20 Years
Sukupuolet, jotka ovat kelpoisia tutkimukseenAll
NäytteenottomenetelmäNon-Probability Sample
Hyväksyy terveelliset vapaaehtoisetJoo
Kriteeri

Inclusion Criteria:

- Clinical diagnosis of oral cancer

- Post-reconstructive surgery

- Age between 20 to 65 years old

- Must be able to follow instructions

Exclusion Criteria:

- Central nervous disease

- Metastasis

Tulokset

Ensisijaiset tulosmittaukset

1. return to work as measured by interview [1 year]

2. quality of life as measured by European Organization for Research and Treatment of Cancer (EORTC) quality of life questionnaire (QLQ)-C30 [1 year]

3. physical functions measured by 6-minute walking test [1 year]

4. quality of life as measured by European Organization for Research and Treatment of Cancer (EORTC) quality of life questionnaire (QLQ)-H&N35 [1 year]

5. physical functions measured by time up & go test [1 year]

Toissijaiset tulosmittaukset

1. shoulder function measured by function-related tests [1 year]

2. pain measured by Visual Analog Scale [1 year]

3. mouth opening measured by Boley gauge [1 year]

4. joint range of motion measured by goniometer [1 year]

5. muscle strength measured by manual muscle testing [1 year]

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