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Tai-Chi and Aerobic Exercise to Improve Emotional Symptom Cluster in Late-stage Lung Cancer Patients

Tai-Chi and Aerobic Exercise to Improve Emotional Symptom Cluster in Late-stage Lung Cancer Patients

Status
Recruiting
Phases
NA
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT05778708
Enrollment
318
Registered
2023-03-21
Start date
2023-03-13
Completion date
2026-10-31
Last updated
2023-05-10

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Advanced Lung Non-Small Cell Carcinoma

Brief summary

The goal of this randomized controlled trial is to investigate the effects of Tai-Chi and aerobic exercise on the emotional symptom cluster, and the underlying mechanism of that cluster, in late-stage lung cancer patients. Participants will be randomized into one of three groups: 1) Tai-Chi group, 2) aerobic exercise group, or 3) self-management control group. Both the Tai-Chi and aerobic exercise groups will attend twice-weekly group classes for 16 weeks (32 total contact hours). The self-management control group will receive written information regarding the recommended level of physical activity.

Detailed description

Late-stage lung cancer patients (n = 318) meeting the inclusion criteria will be recruited and randomized into one of three groups: 1) Tai-Chi group, 2) aerobic exercise group, or 3) self-management control group. Both the Tai-Chi and aerobic exercise groups will attend twice-weekly group classes for 16 weeks (32 total contact hours). The self-management control group will receive written information regarding the recommended level of physical activity. To evaluate the effectiveness of Tai-Chi and aerobic exercise in alleviating the emotional symptom cluster (primary outcome) and individual symptoms (sleep disturbance, anxiety, depression, fatigue), outcome measures will be conducted at baseline, 8 weeks (mid-point assessment), 16 weeks (post-intervention), and 28 weeks (12-weeks post-intervention). A linear mixed-effects model will be used to study the between-group differences in outcomes. In addition, emotion regulation, mindfulness, and cardiorespiratory fitness will be evaluated at each data collection point, and structural equation modeling will be used for subsequent mediation analysis to determine their mediating role in outcome changes. Qualitative interviews will be conducted to understand patients' experience and evaluation of the interventions.

Interventions

BEHAVIORALTai-Chi intervention

The standardized 16-form Yang-style Tai-Chi exercise set will be adopted. Group classes will take place in a community center twice a week for 16 weeks, with each class lasting approximately 60 minutes. Classes will be taught by an experienced Tai-Chi master. Patients will be instructed to practice the Tai-Chi exercises at home at least 3 times a week (30 min each time for a total of 90 min). Patients will be provided with a daily exercise log to record their exercise type, frequency, and intensity.

The aerobic exercise class will be designed to cover both aerobic and resistance exercises. Group classes will take place in an exercise center twice a week for 16 weeks, with each class lasting approximately 60 minutes. Each class will be led by a certified exercise specialist. Patients will be provided with a daily exercise log to record their exercise type, frequency, and intensity.

Sponsors

Queen Mary Hospital, Hong Kong
CollaboratorOTHER
The University of Hong Kong
Lead SponsorOTHER

Study design

Allocation
RANDOMIZED
Intervention model
PARALLEL
Primary purpose
SUPPORTIVE_CARE
Masking
DOUBLE (Investigator, Outcomes Assessor)

Masking description

Except for the primary research assistant who will inform the patients of their group allocation, all researchers on the team will be blinded to patients' group assignment.

Eligibility

Sex/Gender
ALL
Age
18 Years to No maximum
Healthy volunteers
No

Inclusion criteria

* diagnosed with stage IIIB or IV non-small cell lung cancer confirmed by pathology, with no other cancer diagnosis within the previous year; * a current Eastern Cooperative Oncology Group Performance Status of 0-2; * experience of sleep disturbance, anxiety, depression, and fatigue in the past week (rating of 1 or more on a 0-10 numeric rating scale \[NRS\] for each symptom); * able to communicate in Cantonese, Mandarin, or English; * conscious and alert

Exclusion criteria

* suffering from a condition that hinders exercise performance (e.g., active neurological disorder, recent heart attack); * currently participating in any other exercise or mind-body classes; or 3) performing regular exercises, defined as at least 150 minutes of moderate-intensity exercise weekly

Design outcomes

Primary

MeasureTime frameDescription
Change from Baseline Emotional symptom cluster at 8 weeks8 weeksNRSs for assessing each symptom of sleep disturbance, anxiety, depression, and fatigue over the past 7 days will be used to measure emotional symptom cluster severity. Higher score indicates more severe symptoms.
Change from Baseline Emotional symptom cluster at 16 weeks16 weeksNRSs for assessing each symptom of sleep disturbance, anxiety, depression, and fatigue over the past 7 days will be used to measure emotional symptom cluster severity. Higher score indicates more severe symptoms.
Change from Baseline Emotional symptom cluster at 28 weeks28 weeksNRSs for assessing each symptom of sleep disturbance, anxiety, depression, and fatigue over the past 7 days will be used to measure emotional symptom cluster severity. Higher score indicates more severe symptoms.

Secondary

MeasureTime frameDescription
Change from Baseline Sleep disturbance at 16 weeks16 weeksMeasured by the Pittsburg Sleep Quality Index. The total score ranges from 0-21, with higher scores denoting poorer sleep.
Change from Baseline Sleep disturbance at 28 weeks28 weeksMeasured by the Pittsburg Sleep Quality Index. The total score ranges from 0-21, with higher scores denoting poorer sleep.
Change from Baseline Fatigue at 8 weeks8 weeksMeasured by the Brief Fatigue Inventory. Higher score denotes worse fatigue level.
Change from Baseline Fatigue at 16 weeks16 weeksMeasured by the Brief Fatigue Inventory. Higher score denotes worse fatigue level.
Change from Baseline Fatigue at 28 weeks28 weeksMeasured by the Brief Fatigue Inventory. Higher score denotes worse fatigue level.
Change from Baseline Anxiety and depression at 8 weeks8 weeksMeasured by the Hospital Anxiety and Depression Scale. Higher score denotes higher level of anxiety and depression.
Change from Baseline Anxiety and depression at 16 weeks16 weeksMeasured by the Hospital Anxiety and Depression Scale. Higher score denotes higher level of anxiety and depression.
Change from Baseline Anxiety and depression at 28 weeks28 weeksMeasured by the Hospital Anxiety and Depression Scale. Higher score denotes higher level of anxiety and depression.
Change from Baseline Emotion regulation at 8 weeks8 weeksMeasured by the Emotion Regulation Questionnaire. Higher scores indicating greater usage of that strategy.
Change from Baseline Emotion regulation at 16 weeks16 weeksMeasured by the Emotion Regulation Questionnaire. Higher scores indicating greater usage of that strategy.
Change from Baseline Emotion regulation at 28 weeks28 weeksMeasured by the Emotion Regulation Questionnaire. Higher scores indicating greater usage of that strategy.
Change from Baseline Mindfulness at 8 weeks8 weeksMeasured by the Five Facet Mindfulness Questionnaire-Short Form. Higher score denotes higher mindfulness experience.
Change from Baseline balance at 16 weeks16 weeksMeasured by the single-leg standing test; ; unit: second.
Change from Baseline Mindfulness at 28 weeks28 weeksMeasured by the Five Facet Mindfulness Questionnaire-Short Form. Higher score denotes higher mindfulness experience.
Change from Baseline Cardiorespiratory fitness at 8 weeks8 weeksMeasured by the six-minute walk test. The distance walked at the end of 6 minutes will be measured in meters.
Change from Baseline Cardiorespiratory fitness at 16 weeks16 weeksMeasured by the six-minute walk test. The distance walked at the end of 6 minutes will be measured in meters.
Change from Baseline Cardiorespiratory fitness at 28 weeks28 weeksMeasured by the six-minute walk test. The distance walked at the end of 6 minutes will be measured in meters.
Change from Baseline agility at 8 weeks8 weeksMeasured by the timed up-and-go test; unit: second.
Change from Baseline agility at 16 weeks16 weeksMeasured by the timed up-and-go test; unit: second.
Change from Baseline agility at 28 weeks28 weeksMeasured by the timed up-and-go test; unit: second.
Change from Baseline strength at 8 weeks8 weeksMeasured by the sit-to-stand test; unit: number of times.
Change from Baseline strength at 16 weeks16 weeksMeasured by the sit-to-stand test; unit: number of times.
Change from Baseline strength at 28 weeks28 weeksMeasured by the sit-to-stand test; unit: number of times.
Change from Baseline balance at 8 weeks8 weeksMeasured by the single-leg standing test; ; unit: second.
Change from Baseline Mindfulness at 16 weeks16 weeksMeasured by the Five Facet Mindfulness Questionnaire-Short Form. Higher score denotes higher mindfulness experience.
Change from Baseline balance at 28 weeks28 weeksMeasured by the single-leg standing test; ; unit: second.
Change from Baseline Sleep disturbance at 8 weeks8 weeksMeasured by the Pittsburg Sleep Quality Index. The total score ranges from 0-21, with higher scores denoting poorer sleep.

Countries

Hong Kong

Contacts

Primary ContactChia-Chin Lin, PhD,FAAN,RN
cclin@hku.hk39176633
Backup ContactNaomi Takemura, BNurs,PhD,RN
naomitak@connect.hku.hk39176614

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 4, 2026