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Trial Detail

CUHK_CCRB00581

2018-02-07

Prospective

CREC 2016.440

Health Care and Promotion Scheme, Food and Health Bureau, The Government of SAR

Professor Regina Wing Shan SIT

N/A

Take on all the responsibilities of sponsorship jointly with the primary sponsor

Lyan Chow Lai yan

Room 04, 4/F, Lek Yuen Health Centre, 9 Lek Yuen Street, Shatin, N.T., Hong Kong

95403121

chowlyan@cuhk.edu.hk

Division of Family Medicine and Primary Health Care, The Jockey Club School of Public Health and Primary Care, The Chinese University of Hong Kong

Hong Kong

Regina Wing Shan SIT

Room 17A, 4/F, Lek Yuen Health Centre, 9 Lek Yuen Street, Shatin, N.T., Hong Kong

25039053

reginasit@cuhk.edu.hk

Division of Family Medicine and Primary Health Care, The Jockey Club School of Public Health and Primary Care, The Chinese University of Hong Kong

Hong Kong

Clinical effectiveness of a neuromuscular training exercise based pain management program for community-dwelling elders with chronic musculoskeletal pain: a pragmatic randomized trial

Neuromuscular training exercise for Chronic Musculoskeletal Pain

長者慢性肌骼痛症運動治療研究計劃

Hong Kong

Yes

2016-12-14

Joint CUHK-NTEC Clinical Research Ethics Committee

2016.440

chronic musculoskeletal pain

Behavior

Neuromuscular training exercise

NA

12 classes

6 weeks

Twice a week

Waiting list control

Elderly exercise pamphlets

NA

12 weeks

NA

(i) community-dwelling older adults (age ≥65 years)

(ii) mobile over 10 m with or without a walking aid

(iii) present of chronic musculoskeletal pain over the past month and for at least 3 month of the previous year

(iv) pain intensity score ≥ 3 on a numerical rating scale of 10

(v) stable baseline activity

(vi) able to understand written and verbal Chinese

(i) dementia or mild cognitive impairment (including those showing any signs of cognitive impairment as advised by the scheme manager/medical records)

(ii) Musculoskeletal pain due to uncontrolled rheumatic disease

(iii) a recent self-reported history of stroke or major surgery (in the past 6 months)

(iv) terminally ill

(v) has a serious mental illness

(vi) comorbid conditions which might interfere with the participant's active participation in the study

(vii) severe or uncontrolled heart disease

(viii) participants with major joint replacement or spinal surgery

(ix) participants who fulfil the diagnostic criteria of Chronic Fatigue Syndrome (CFS) by the Center of Disease Control, which is a debilitating and complex disorder characterized by intense fatigue, which worsens with physical and mental exertion, with widespread pain as one of its presentations

65

99

Both Male and Female

Interventional

Randomized

1:1 randomization

Active

Open label

Parallel

2

2018-02-20

72

Complete

The Brief Pain Inventory

self-report

week 0, 6, 12

Pain Self-Efficacy Questionnaire (PSEQ)

self-report

week 0, 6, 12

Timed up and go test

functional assessment

week 0, 6, 12

Grip strength

functional assessment

week 0, 6, 12

General Anxiety Disorder (GAD-7)

self report

week 0, 6, 12

Patient Health Questionnaire (PHQ-9)

self-report

week 0, 6, 12

Health Survey (SF-12)

self-report

week 0, 6,12

Instrumental Activities of Daily Living Scale (IADL)

self report

week 0

Frailty Scale

self-report

week 0

Sarcopenia Assessment

self-report

week 0

Physical Activity Scale for the Elderly (PASE)

self-report

week 0

Stanford Expectations of Treatment Scale (SETS)

self-report

week 0

No

2019-10-22

ChiCTR1800014890

2018-02-07

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