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临床试验/NCT05919446
NCT05919446招募中不适用

The Feasibility, Potential Efficacy, and Experiences of Using a Group-based Acceptance and Commitment Therapy Among Older People With Chronic Low Back Pain: a Pilot Randomized Controlled Trial

The Hong Kong Polytechnic University1 个研究点 分布在 1 个国家目标入组 30 人开始时间: 2023年8月1日最近更新:
适应症
干预措施

试验速览

阶段
不适用
状态
招募中
入组人数
30
试验地点
1
主要终点
Change from baseline of psychological flexibility at immediately after the 4-week treatments

研究概览

简要总结

No study has investigated the effects of ACT on community-dwelling Chinese older adults. Given that clinical practice guidelines have recommended exercise therapy for treating people with CLBP, a combination of ACT and exercise therapy may yield better clinical outcomes than exercise alone among community-dwelling older adults with CLBP. A double-blinded (participants and statistician) pilot randomized controlled trial (RCT) will be conducted to evaluate the feasibility and the relative effects of ACT plus back exercise training as compared to exercise alone in improving psychological flexibility, physical wellbeing, and quality of life of community-dwelling older people with CLBP. Further, a qualitative research study will be conducted to understand the experiences of participating in ACT and back exercise training in older people with CLBP (including identifying facilitators and barriers to participation).

详细描述

Participants will be recruited from rehabilitation clinics, or community centres by posters posted in these locations. A total of 30 older people with LBP will be recruited and randomized into either a 4-week ACT plus back exercise group, or a back exercise control group. Immediately after the 4-week treatment, participants will be invited to complete another set of questionnaires that are identical to their baseline questionnaires to evaluate the effects of interventions on their pain, physical function, psychological wellbeing, and quality of life. At 3-month post-treatment, participants will be invited to complete the identical questionnaires again.

研究设计

研究类型
Interventional
分配方式
Randomized
干预模型
Parallel
主要目的
Prevention
盲法
Double (Participant, Investigator)

盲法说明

double-blinded (participants and statistician)

入排标准

年龄范围
60 Years 至 —(Adult, Older Adult)
性别
All
接受健康志愿者

入选标准

  • have non-specific LBP in or near the lumbosacral spine with or without leg pain that lasts for at least 3-months in the last 12 months
  • have sought some medical or healthcare professional treatments for CLBP
  • able to read and write at an adequate level of proficiency in Chinese
  • Mini-Mental Status Examination (MMSE) scores 23 or above

排除标准

  • people with malignant pain or lumbar spinal stenosis
  • confirmed dementia
  • severe cognitive impairment
  • serious psychiatric or psychological disorders
  • Mini-Mental Status Examination (MMSE) scores below 23

研究组 & 干预措施

Older people without ACT intervention

Other

4-week back exercise control group

干预措施: back exercise (Behavioral)

Older people with ACT intervention

Experimental

4 week ACT plus back exercise group

干预措施: Acceptance and commitment therapy (ACT) (Behavioral)

Older people with ACT intervention

Experimental

4 week ACT plus back exercise group

干预措施: back exercise (Behavioral)

结局指标

主要结局

Change from baseline of psychological flexibility at immediately after the 4-week treatments

时间窗: Baseline and at immediately after the 4-week treatments

The 7-item Chinese version of the Acceptance and Action Questionnaire II (AAQ-II) will be used to measure participants' psychological flexibility. It comprises 7 statements, which are rated on a 7-point scale, where 1 means "never true" and 7 means "always true." The maximum total score is 49. Higher total scores mean less flexibility. AAQ-II has been cross-culturally adapted and validated among local adolescents and has demonstrated satisfactory internal consistency and test-retest reliability.

次要结局

  • Change of LBP intensity(Baseline, immediately after the 4-week treatments, and at 3-month post-treatment)
  • Change of LBP-related disability(Baseline, immediately after the 4-week treatments, and at 3-month post-treatment)
  • Overall perceived changes in symptom severity, treatment response and the efficacy of treatment(Baseline, immediately after the 4-week treatments, and at 3-month post-treatment)
  • Change of depression, anxiety, and stress(Baseline, immediately after the 4-week treatments, and at 3-month post-treatment)
  • Change from baseline of psychological flexibility at 3-month post-treatment(Baseline and at 3-month post-treatment)
  • Change of health-related quality of life(Baseline, immediately after the 4-week treatments, and at 3-month post-treatment)

研究者

申办方类型
Other
责任方
Principal Investigator
主要研究者

Dr Arnold Wong Yu Lok

Associate Professor

The Hong Kong Polytechnic University

研究点 (1)

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