Trial · NCT06709963
Registered outcomes18
Each outcome the trial registered, primary first, in ClinicalTrials.gov's words.
1 to 18 of 18
Download this page as JSON| List | Outcome | Time frame | Description |
|---|---|---|---|
| Primary | The recruitment rate, retention rate (completion rate), non-completion reasons, drop-out rate | Immediately after the intervention | The recruitment rate, retention rate (completion rate), non-completion reasons, drop-out rate will be evaluated as our primary outcomes, because of the feasibility of the study. |
| Primary | ITBS acceptability questionnaire | Immediately after the intervention | ITBS acceptability questionnaire has ten items of positive acceptability, ranged from 10 to 50, and it also has five items of negative acceptability, ranged from 5 to 25. The iTBS acceptability questionnaire has a total score ranging from 15 to 75. |
| Primary | Pain intensity assessment | Baseline, immediately after the intervention, five-month follow-up at one-month,three-month,six-month follow-up timepoints. | The 11-point numerical rating scale, ranged from 0 to 10, higher scores indicate higher pain intensity. |
| Secondary | Depression, anxiety, and stress test | Baseline | The Chinese version of the short Depression Anxiety Stress Scales, scores ranged from 0 to 13, higher scores for each domain (depression, anxiety, and stress) indicate more respective problems. |
| Secondary | Disability evaluation | Baseline, immediately after the intervention, five-month follow-up at one-month,three-month,six-month follow-up timepoints. | The Hong Kong Chinese Version of the Roland-Morris Disability Questionnaire has 24 items. Scores ranged from 0 to 24, higher scores indicate worse disability. |
| Secondary | Pain catastrophizing assessment | Baseline, immediately after the intervention, five-month follow-up at one-month,three-month,six-month follow-up timepoints. | The Chinese version of Pain Catastrophizing Score. The scores ranged from 0 to 13, higher scores indicate more pain catatrophizing thought. |
| Secondary | Pain drawing test | Baseline | The body map scoring system indicates the location of participants' painful site |
| Secondary | Frailty status assessment | Baseline, immediately after the intervention, one-month follow-up timepoint. | Fatigue, Resistance, Ambulation, Illness, and Loss, the presence of 3 of 5 item characteristics indicate the presence of frailty, scores ranged from 0 to 5. Lower scores mean more frailty. |
| Secondary | Physical activity assessment | Baseline, immediately after the intervention, one-month follow-up timepoint. | Physical Activity Scale for the Elderly; it has 3 domains (leisure, household, and occupation activities) to measure physical activity levels of adults aged 65 or above. higher scores indicate more active. |
| Secondary | Sleep quality assessment | Baseline, immediately after the intervention, one-month follow-up timepoint. | Pittsburgh Sleep Quality Index. It has 7 domains to measure sleep quality , sleep latency, sleep duration, habital sleep efficiency, sleep disturbances, use of sleep medication, and daytime dysfunction. Scores ranged from 0 to 21, higher scores indicate poorer sleep quality. |
| Secondary | Cognitive function screening | Baseline | Hong Kong Montreal Cognitive Assessment. It is a cognitive screening tool specifically adapted for Chinese older adults in Hong Kong. It is designed to detect mild cognitive impairment and dementia. A score \< 26 suggests participant has mild cognitive impairment. |
| Secondary | Working memory test inside magnetic resonance imaging scanning | Baseline, immediately after the intervention | The digit 2-back task, more response accuracy of digits indicates better working memory |
| Secondary | Cognitive flexibility test inside magnetic resonance imaging scanning | Baseline, immediately after the intervention. | The More Odd Shifting task, It requires participants to switch between different mental sets or rules, such as identifying odd numbers or shifting between different categories. Better response accuracy indicates better cognitive flexibility |
| Secondary | Cognitive inhibition test inside magnetic resonance imaging scanning | Baseline, immediately after the intervention. | Color-Word Matching Stroop Task, more correct matching indicate better ability to inhibit cognitive interference |
| Secondary | Perseveration and abstract reasoning test outside magnetic resonance imaging scanning | Baseline, immediately after the intervention, one-month follow-up timepoint. | The Modified Wisconsin Card Sorting Test, more correct matching of cards indicate better perseveration and abstract reasoning. |
| Secondary | Working memory Test outside magnetic resonance imaging scanning | Baseline, immediately after the intervention, one-month follow-up timepoint. | The Verbal Digits Forward and Backward Test, more correct recall of digits indicate better working memory and executive function |
| Secondary | Cognitive flexibility test outside magnetic resonance imaging scanning | Baseline, immediately after the intervention, one-month follow-up timepoint. | The Trail Making Tests, a neuropsychological test of visual attention and task switching, completing the trail correctly within a shorter period of time means better cognitive flexibility |
| Secondary | Inhibition test outside magnetic resonance imaging scanning | Baseline, immediately after the intervention, one-month follow-up timepoint. | Go/NoGo task, more response accuracy indicates better control of inhibition. |
Source ClinicalTrials.govtrials-2026-11-12-0.5.0
Sources 3
- ClinicalTrials.gov's posted results, through CTTI's AACTFreely available. Acknowledgement requested
- ClinicalTrials.govNo license stated
- NIH RePORTER's clinical studies and project filesPublic domain
Each source's terms
- ClinicalTrials.gov's posted results, through CTTI's AACTClinicalTrials.gov data via Aggregate Analysis of ClinicalTrials.gov (AACT), CTTI. CTTI makes its materials freely available and requests acknowledgement. https://aact.ctti-clinicaltrials.org/documentation/299
- ClinicalTrials.govnone stated
- NIH RePORTER's clinical studies and project filesPublic domain (NIH RePORTER)
ClinicalTrials.gov's data carry an international copyright outside the United States: https://clinicaltrials.gov/about-site/terms-conditions.
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