Journal of Traditional Chinese Medicine ›› 2026, Vol. 46 ›› Issue (5): 1295-1306.DOI: 10.19852/j.cnki.jtcm.2026.05.022
• Idea and Methodology • Previous Articles Next Articles
FANG Ge1,2, LI Lin2, LI Xiantao3, CHEN Jiaxu4, ZHOU Xuan4, HU Zhixi2(
)
Received:2025-02-12
Accepted:2025-12-24
Online:2026-10-15
Published:2026-10-09
Contact:
Prof. HU Zhixi, School of Traditional Chinese Medicine, Hunan University of Chinese Medicine, Changsha 410208, China. 003405@hnucm.edu.cn,Telephone: +86-18719139564
Supported by:FANG Ge, LI Lin, LI Xiantao, CHEN Jiaxu, ZHOU Xuan, HU Zhixi. Quality criteria for measuring properties of diagnostic scale for Traditional Chinese Medicine syndromes[J]. Journal of Traditional Chinese Medicine, 2026, 46(5): 1295-1306.
| Property | Definition | Quality criteria |
|---|---|---|
| Literature review | Systematically collects disease descriptions in the TCM literature, organizes physicians’ experience, and provides basic data to establish scale items | + A good search strategy; Clear inclusion/exclusion criteria; Quantified and graded |
| − No searched strategy; Vague inclusion and exclusion criteria; Not quantified and graded | ||
| Clinical data | Primarily cross-sectional and retrospective studies | + The pool of the top 20 items and the remaining low-frequency words are selected as alternative items |
| − All items are considered alternate items | ||
| Subjective screening | Delphi method, soliciting experts’ anonymous opinions of the item pool | + (a) Expert concentration: average >2 (rate 0-4), grade sum >30% of full score ratio, and full score ratio >30% and (b) expert coordination coefficient: coordination coefficient >0.1 |
| − (a) Expert concentration: average ≤2 (rate 0-4), grade sum ≤30% of full score ratio, and full score ratio ≤30%; and (b) expert coordination coefficient: coordination coefficient ≤0.1 | ||
| Objective screening | The extent to which the results of participant interviews are examined using various statistical methods | + (a) Item distribution inspection method: a response rate ≤80% for any option; (b) t-test: P-value < 0.05; (c) discrete trend method: S ≥0.9; (d) correlation coefficient method: correlation coefficient of ≥0.4; and (e) Cronbach’s α coefficient method: If Cronbach’s α changes little, it is retained |
| − (a) Item distribution inspection method: a response rate >80% in any option; (b) t-test: P-value ≥0.05; (c) discrete trend method: S < 0.9; (d) correlation coefficient method: correlation coefficient of < 0.4; and (e) Cronbach’s α coefficient method: If Cronbach’s α increases significantly, consider deleting the item | ||
| Item weighting methods | Items were quantified | + Formulas used to determine item scores |
| − No formulas used to determine item scores | ||
| Diagnostic threshold | ROC analysis | + ROC curve of >0.6 |
| − ROC curve of ≤0.6 | ||
| Internal consistency | Items in a (sub)scale are intercorrelated, thus measuring the same construct | + Cronbach’s α: 0.70-0.90 |
| − Cronbach’s α: < 0.70 or >0.90 | ||
| Split-half | Test of how consistently a quantity is represented across items | + Cronbach’s α: 0.70-0.90 |
| − Cronbach’s α: < 0.70 or >0.90 | ||
| Test-retest | After the scale measures the same measurement object, it is re-measured using the same scale within a certain period (less than two weeks) | + ICC or weighted kappa is ≥0.40 |
| − ICC or weighted kappa is < 0.40 | ||
| Interrater consistency | Clinicians from multiple centers with different backgrounds and professional knowledge of Chinese medicine | + ICC or weighted kappa is ≥0.40; and ≥10 clinicians |
| − ICC or weighted kappa is < 0.40; and < 10 clinicians | ||
| Content validity | Degree of coincidence between the content actually measured by a scale and the content to be measured | + I-CVI >0.78 and S-CVI >0.80 |
| − I-CVI ≤0.78 and S-CVI ≤0.80 | ||
| Criterion validity | Correlation between the scale and gold standard | + correlation coefficient is >0.70 |
| − correlation coefficient is ≤0.70 | ||
| Structural validity | Degree of correlation between specific construct items, which is consistent with the theoretical hypothesis | + CFA: RMSEA < 0.08, and GFI, AGFI, NFI, IFI, TLI, and CFI >0.80 |
| − CFA: RMSEA ≥0.08, and GFI, AGFI, NFI, IFI, TLI, and CFI ≤0.80 | ||
| Convergent validity | Computed from the hypothesis item-subscale correlation | + correlation coefficient ≥0.40 |
| − correlation coefficient < 0.40 | ||
| Discriminant validity | Comparing and analyzing score differences in different characteristic populations | + t-test: t >1 and P < 0.05. |
| − t-test: t ≤1 and P ≥0.05. |
Table 1 Quality criteria for the property measurements of the diagnostic criteria for TCM syndromes
| Property | Definition | Quality criteria |
|---|---|---|
| Literature review | Systematically collects disease descriptions in the TCM literature, organizes physicians’ experience, and provides basic data to establish scale items | + A good search strategy; Clear inclusion/exclusion criteria; Quantified and graded |
| − No searched strategy; Vague inclusion and exclusion criteria; Not quantified and graded | ||
| Clinical data | Primarily cross-sectional and retrospective studies | + The pool of the top 20 items and the remaining low-frequency words are selected as alternative items |
| − All items are considered alternate items | ||
| Subjective screening | Delphi method, soliciting experts’ anonymous opinions of the item pool | + (a) Expert concentration: average >2 (rate 0-4), grade sum >30% of full score ratio, and full score ratio >30% and (b) expert coordination coefficient: coordination coefficient >0.1 |
| − (a) Expert concentration: average ≤2 (rate 0-4), grade sum ≤30% of full score ratio, and full score ratio ≤30%; and (b) expert coordination coefficient: coordination coefficient ≤0.1 | ||
| Objective screening | The extent to which the results of participant interviews are examined using various statistical methods | + (a) Item distribution inspection method: a response rate ≤80% for any option; (b) t-test: P-value < 0.05; (c) discrete trend method: S ≥0.9; (d) correlation coefficient method: correlation coefficient of ≥0.4; and (e) Cronbach’s α coefficient method: If Cronbach’s α changes little, it is retained |
| − (a) Item distribution inspection method: a response rate >80% in any option; (b) t-test: P-value ≥0.05; (c) discrete trend method: S < 0.9; (d) correlation coefficient method: correlation coefficient of < 0.4; and (e) Cronbach’s α coefficient method: If Cronbach’s α increases significantly, consider deleting the item | ||
| Item weighting methods | Items were quantified | + Formulas used to determine item scores |
| − No formulas used to determine item scores | ||
| Diagnostic threshold | ROC analysis | + ROC curve of >0.6 |
| − ROC curve of ≤0.6 | ||
| Internal consistency | Items in a (sub)scale are intercorrelated, thus measuring the same construct | + Cronbach’s α: 0.70-0.90 |
| − Cronbach’s α: < 0.70 or >0.90 | ||
| Split-half | Test of how consistently a quantity is represented across items | + Cronbach’s α: 0.70-0.90 |
| − Cronbach’s α: < 0.70 or >0.90 | ||
| Test-retest | After the scale measures the same measurement object, it is re-measured using the same scale within a certain period (less than two weeks) | + ICC or weighted kappa is ≥0.40 |
| − ICC or weighted kappa is < 0.40 | ||
| Interrater consistency | Clinicians from multiple centers with different backgrounds and professional knowledge of Chinese medicine | + ICC or weighted kappa is ≥0.40; and ≥10 clinicians |
| − ICC or weighted kappa is < 0.40; and < 10 clinicians | ||
| Content validity | Degree of coincidence between the content actually measured by a scale and the content to be measured | + I-CVI >0.78 and S-CVI >0.80 |
| − I-CVI ≤0.78 and S-CVI ≤0.80 | ||
| Criterion validity | Correlation between the scale and gold standard | + correlation coefficient is >0.70 |
| − correlation coefficient is ≤0.70 | ||
| Structural validity | Degree of correlation between specific construct items, which is consistent with the theoretical hypothesis | + CFA: RMSEA < 0.08, and GFI, AGFI, NFI, IFI, TLI, and CFI >0.80 |
| − CFA: RMSEA ≥0.08, and GFI, AGFI, NFI, IFI, TLI, and CFI ≤0.80 | ||
| Convergent validity | Computed from the hypothesis item-subscale correlation | + correlation coefficient ≥0.40 |
| − correlation coefficient < 0.40 | ||
| Discriminant validity | Comparing and analyzing score differences in different characteristic populations | + t-test: t >1 and P < 0.05. |
| − t-test: t ≤1 and P ≥0.05. |
| Scale | TCM functional gastrointestinal disorders scale | TCM syndrome differentiation instrument for functional gastrointestinal disorders | TCM syndrome differentiation instrument for functional gastrointestinal disorders (amended) | TCM functional dyspepsia scale | Stomach Qi defificiency pattern assessment scale | ||
|---|---|---|---|---|---|---|---|
| Establishment of an item pool | Literature review | + | + | + | + | + | |
| Clinical data | + | − | − | − | − | ||
| Item screening methods | Subjective screening | − | − | − | − | + | |
| Objective screening | + | + | + | + | − | ||
| Item weighting methods | − | − | − | + | − | ||
| Diagnostic threshold | − | − | − | + | + | ||
| Clinical evaluation | Reliability | Internal consistency | + | − | − | − | + |
| Split-half | + | − | − | − | − | ||
| Test-retest | − | − | − | + | − | ||
| Inter-rater consistency | − | − | − | − | − | ||
| Validity | Content validity | + | − | − | − | − | |
| Criterion validity | − | − | − | + | + | ||
| Structural validity | + | + | + | − | − | ||
| Convergent validity | − | − | − | − | − | ||
| Discriminant validity | + | + | − | − | − | ||
Table 2 Summary of the assessment of measurement properties among TCM diagnostic scales for functional dyspepsia
| Scale | TCM functional gastrointestinal disorders scale | TCM syndrome differentiation instrument for functional gastrointestinal disorders | TCM syndrome differentiation instrument for functional gastrointestinal disorders (amended) | TCM functional dyspepsia scale | Stomach Qi defificiency pattern assessment scale | ||
|---|---|---|---|---|---|---|---|
| Establishment of an item pool | Literature review | + | + | + | + | + | |
| Clinical data | + | − | − | − | − | ||
| Item screening methods | Subjective screening | − | − | − | − | + | |
| Objective screening | + | + | + | + | − | ||
| Item weighting methods | − | − | − | + | − | ||
| Diagnostic threshold | − | − | − | + | + | ||
| Clinical evaluation | Reliability | Internal consistency | + | − | − | − | + |
| Split-half | + | − | − | − | − | ||
| Test-retest | − | − | − | + | − | ||
| Inter-rater consistency | − | − | − | − | − | ||
| Validity | Content validity | + | − | − | − | − | |
| Criterion validity | − | − | − | + | + | ||
| Structural validity | + | + | + | − | − | ||
| Convergent validity | − | − | − | − | − | ||
| Discriminant validity | + | + | − | − | − | ||
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