alexa Review of the Steps for Development of Quantitative Research Tools | OMICS International
ISSN 2573-0347
Advanced Practices in Nursing
Like us on:
Make the best use of Scientific Research and information from our 700+ peer reviewed, Open Access Journals that operates with the help of 50,000+ Editorial Board Members and esteemed reviewers and 1000+ Scientific associations in Medical, Clinical, Pharmaceutical, Engineering, Technology and Management Fields.
Meet Inspiring Speakers and Experts at our 3000+ Global Conferenceseries Events with over 600+ Conferences, 1200+ Symposiums and 1200+ Workshops on
Medical, Pharma, Engineering, Science, Technology and Business

Review of the Steps for Development of Quantitative Research Tools

Ashok Kumar*

College of Nursing, All India Institute of Medical Sciences, Jodhpur Rajasthan, India

*Corresponding Author:
Ashok Kumar
Assistant Professor
College of Nursing
All India Institute of Medical Sciences
Jodhpur, Rajasthan, India
Tel: 8003996929
E-mail: [email protected]

Received date: October 31, 2015; Accepted date: December 21, 2015; Published date: December 30, 2015

Citation: Kumar A (2015) Review of the Steps for Development of Quantitative Research Tools. Adv Practice Nurs 1:103. doi:10.4172/apn.1000103

Copyright: © 2015 Kumar A. This is an open-access article distributed under the terms of the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are credited.

Visit for more related articles at Advanced Practices in Nursing


The number of tools developed by researchers has increased in recent years. Still the demand and need for development of new and standardized tool is increasing to a great extent, the simple reason is either standardized tools are not available or available tools lacks reliability and validity in that setting. This article explores the steps and process which provides base by which a reliable and valid tool can be developed. Method followed was indepth review of published research articles. This article reviews tool development procedures used in 17 articles published in leading journals from 1992 to 2007. It points out the steps of tool development viz. item generation in which theoretical basis to be used. Next step is reliability in that internal consistency, equivalence by inter-rater and stability by test-retest method is checked; validity i.e. face, content, concurrent and construct validity to be calculated. Further in construct validity factor analysis including principal component analysis, pre-analysis checks and factor extraction is to be analysed. Based on the review, the author mentioned the steps of tool development which will guide researchers to improve the tool development process.


Tool development; Item generation; Reliability; Validity


There are a range of scales and response styles that may be used when developing a tool. These produce different types or levels of data and this will influence the analysis options. Therefore, when developing a new measure, it is important to be clear which scale and response format to use [1].

In developing the evidence base of practice using this method of data collection, it is vital that tool design incorporates pre planned methods to establish reliability and validity. Failure to develop a tool sufficiently may lead to difficulty interpreting results, and this may impact upon clinical or educational practice. Hinkin and DeVellis state that the construction of a new tool is a highly complex process. Several steps are required to develop a multi-item tool to measure a construct. The researcher needs to:

- apply a theoretical basis to develop the items;

- design the individual items;

- conduct an item analysis to eliminate poor items (ambiguous, no variation);

- assess the reliability of tool i.e. internal consistency, stability and equivalence;

- determine the construct validity of the measure using factor analysis;

- determine the convergent validity of the measure; and

- determine the divergent validity (discriminant validity, including method effects) [2,3].

The researcher also needs to determine the level of specificity required of the scale. This will largely be determined by the research question, as the level of specificity of the scale should align with the level of specificity of the research question and the other constructs it will be compared with [3].

Item Generation: Use a Theoretical Basis

As a first step to tool development, the researcher should carefully examine the extant theory relating to the construct he or she wishes to measure. Theory can provide a guide in terms of developing the conceptual formulations required for operationalization. Examining theory helps to establish the parameters of the construct to ensure that the content of the scale is focused on the actual domain of interest, rather than unrelated areas [3].

The researcher should develop the items from a theory of the construct (latent variable) so that they are consistent with it. If there is a theoretical basis for this construct, it can be defined and the type of relationships it has with other constructs can be predicted. The generation of items during tool development requires considerable pilot work to refine wording and content. In addition, a key strategy in item generation is to revisit the research questions frequently and to ensure that items reflect these and remain relevant. During this stage that the proposed subscales of a tool are identified and to ensure that items are representative of these. The item and factor analysis stages of the tool development process may then be used to establish if such items are indeed representative of the expected subscale or factor [4,5].

Once the researcher has generated the initial pool of items, the next step involves having a panel of subject-matter expert’s review the items in terms of content adequacy. These experts should be provided with construct definitions and instructed to sort the items according to these definitions, to determine whether their sort aligns with the scale developer’s conceptualisations [6].

To assure face or content validity, items can be generated from a number of sources including consultation with experts in the field, proposed respondents and review of associated literature. The type of tool, language used and order of items may all bias response.

Consideration should be given to the order in which items are presented, e.g. it is best to avoid presenting controversial or emotive items at the beginning of the tool. To engage participants and prevent boredom, demographic and/or clinical data may be presented at the end. Certain questions should be avoided, e.g. those that leads or includes double negatives or double-barrelled questions [5]. A mixture of both positively and negatively worded items may minimize the danger of acquiescent response bias, i.e. the tendency for respondents to agree with a statement, or respond in the same way to items [7].

To allow respondents to expand upon answers and provide more indepth responses, free text response or open statements/ questions may be included. Respondents may welcome this opportunity. However, whilst this approach can provide the inter-viewer with rich data, such material can be difficult to analyse and interpret. However, these problems may be outweighed by the benefits of including this option and can be especially useful in the early development of a tool. Free text comments can inform future tool development by identifying poorly constructed items or new items for future inclusion [8].


Reliability is an essential issue in scale development and refers to the amount of variance attributable to the true score of the latent construct.3 Reliability refers to the repeatability, stability or consistency of a tool. One form of reliability, internal consistency, is determined by calculating coefficient alpha/ Cronbach’s alpha statistic. This statistic uses inter-item correlations to determine whether constituent items are measuring the same domain. Internal consistency refers to the homogeneity of items within a scale [9]. This coefficient should be as high as possible. If not, items contributing to low reliability (low item to total correlations) need to be dropped and new items developed. If the items show good internal consistency, Cronbach’s alfa should exceed 0.70 for a developing tool or 0.80 for a more established tool. It is usual to report the Cronbach’s alpha statistic for the separate domains within a tool rather for the entire tool. Reliability is a necessary pre-condition for validity [7] (Table 1).

Tool development Key issues Decision aids
Piloting the tool Spread of responses across options High endorsement of a single option is problematic.
Item analysis Initial analysis An item should be considered for removal if ≥80%, ≤20% of responses endorsed one response.
  Clarity and relevance of items Items with an inter-item correlation of <0.3 or >0.7 should be considered for removal.
  Items deemed theoretically important Is your measure affected by social desirability bias? Items with a poor Cronbach’s a, i.e. <0.7 should be considered for removal
    Researcher’s interpretation of patient comments.
Alternatively, if respondents fail to complete an item it suggests that the item may lack clarity.
Items should be retained if they are deemed to be theoretically important even if they do not meet the above criteria.
Explore the relationship between item and scale total with measure that captures this response tendency, e.g. Marlowe-Crown Social Desirability Index.
Reliability Internal consistency Corrected inter-item correlations
  Test-retest Item-total correlation
  Inter-observer Cronbach alpha
    Coefficient correlations
Validity Face or content Do the items sufficiently represent different hypothesized domains?
  Concurrent or discriminant Do subscale scores correlate with existing, validated measures presented concurrently?
  Predictive Do subscale scores predict hypothesis reports on existing, validated measures presented longitudinally?

Table 1: Stages in tool development: (Rattray et al.) [1].

Item-total correlations can also be used to assess internal consistency. If the items are measuring the same underlying concept then each item should correlate with the total score from the tool or domain [4]. This score can be biased, especially in small sample sizes, as the item itself is included in the total score. Therefore, to reduce this bias, a corrected item-total correlation should be calculated. This removes the score from the item from the total score from the tool or domain prior to the correlation. Kline recommends deleting any tool item with a corrected item-total correlation of <0.30. Item analysis using interitem correlations will also identify those items that are too similar. High inter-item correlations (>0.80) suggest that these are indeed repetitions of each other (sometimes referred to as bloated specifics) and are in essence asking the same question [10].

Test–retest reliability can assess stability of a measure over time and this should be included in the process of any tool development. This is of particular importance if the intended use of the measure is to assess change over time or responsiveness [11].

Equivalence in the context of reliability assessment primarily concerns the degree to which two or more independent observers or coders agree about scoring. For this the inter-rater reliability to be calculated by Cohen’s kappa and values of 0.75 or higher are considered very good [12].


Validity refers to whether a tool is measuring what it purports to. While this can be difficult to establish, demonstrating the validity of a developing measure is vital [7]. There are several different types of validity. Content validity (or face validity) refers to expert opinion concerning whether the scale items represent the proposed domains or concepts the tool is intended to measure. This is an initial step in establishing validity, but is not sufficient by itself. Convergent (or concurrent) and discriminant validity must also demonstrated by correlating the measure with related and/or dissimilar measures [5].

The researcher would obtain measures of the scale from a sample from whom he or she also obtained measures of constructs the scale should be related to, including alternative measures of the construct of interest (convergent validity), and of constructs the scale should not be related to (divergent validity). These relationships are calculated by correlation coefficients (e.g., a Pearson product moment correlation coefficient). When developing a tool it is, therefore, important to include, within the research design, additional established measures with proven validity against which to test the developing tool. Construct validity relates to how well the items in the tool represent the underlying conceptual structure. Factor analysis is one statistical technique that can be used to determine the constructs or domains within the developing measure. This approach can, therefore, contribute to establishing construct validity [1].

Factor Analysis

The purpose of an exploratory factor analysis is to analyse scores on several items to see if they can be reduced to underlying dimensions. Those items that are highly related to each other will load on one factor. The items that are measuring one construct should load on one factor and those measuring another construct should load on a different factor. Analyses that yield no clear factors or one factor (for a unidimensional scale) are problematic. Additionally, the factor analysis should explain a substantial amount of the variance in the scores. Based on these factor loadings, the researcher needs to decide which items from the scale should be retained or deleted [1,3].

Following initial pilot work and item deletion, the tool should be administered to a sample of sufficient size to allow exploratory factor analytic techniques to be performed. Ferguson and Cox suggest that 100 respondents is the absolute minimum number to be able to undertake this analysis. However, others would suggest that this is insufficient and a rule of thumb would be five respondents per item [13].

Principal components analysis (PCA) explores the interrelationship of variables. It provides a basis for the removal of redundant or unnecessary items in a developing measure and can identify the associated underlying concepts, domains or subscales of a questionnaire [14]. The terms of factor analysis and PCA are often used synonymously in this context. In practice, however, PCA is most commonly used. Rarely is a tool uni-dimensional and PCA usually identifies the presence of one principal component that accounts for most of the variance and subsequent components that account for less and less [15].

In the initial PCA analysis of an unrotated solution, most items should ‘load’, i.e. correlate with the first component. This can make interpretation of results difficult, and to assist the interpretation of a factor solution, rotation of factors (components) is often performed. Factor rotation maximizes the loadings of variables with a strong association with a factor, and minimizes those with a weaker one and often helps make sense of the proposed factor structure. Varimax rotation, which is an orthogonal rotation (i.e. one in which the factors do not correlate), is often used, particularly if the proposed factors are thought to be independent of each other [13]. However, oblimin rotation may be used, when factors are thought to have some relationship. It is, therefore, vital to state a priori the number of factors you expect to emerge and to have decided which rotation method you will use ahead of any analysis [10].

Pre-analysis Checks

Ferguson and Cox give a detailed account of the process of exploratory factor analysis and provide a set of heuristics for its stages of pre-analysis checks, extraction and rotation (Table 2 for the pre-analysis checks). These pre-analysis checks are necessary to ensure the proposed data set is appropriate for the method. The checks include determining the stability of the emerging factor structure, sampling requirements, item scaling, skewness and kurtosis of variables and the appropriateness of the correlation matrix [13].

Tool development Key issues Pre-analysis checks (Ferguson and Cox) [13]
Further development: Principal components analysis (PCA): Stable Factor Structure
Exploratory Factor analysis Explores the inter-relationship of variables Minimum number of participants: 100
  Provides a basis for the removal of redundant or unnecessary items, PCA is used to identify the underlying domains or factors within a measure. Minimum participant to variable ratio, N/p: 2:1-10:1
    Minimum variable to factor ratio, p/m: 2:1-6:1
  Prior to analysis, must propose an underlying theoretical structure. Minimum participant to factor ratio, N/m: 2:1-6:1
  Ensure that the data set is appropriate Sampling
  Must follow a predefined and systematic analytic  Sequence Random sampling from a population.
    Item scaling
Likert, Mokken and frequency scales are acceptable.
Normality of distribution/skewness and Kurtosis
Underlying assumption is of normal distribution. Values of skewness and kurtosis should be calculated for each variable, and values out with accepted levels dealt with appropriately.
Appropriateness of the correlation matrix Kaiser Meyer-Olkin: can the correlations between variables be accounted for by a smaller set of factors? should be >0.5.
Bartlett Test of Sphericity: based on the chi-squared test, - a large and significant test used to indicate discoverable relationships.
Further development: Allows the further testing of the construct Confirmation of factor structure on an  independent data set, using exploratory and confirmatory methods.
Confirmatory factor analysis Validity of the measure Same underlying assumptions as exploratory methods.
    Confirmatory process uses single sample and multi-sample approaches.

Table 2: Stages in tool development: factor analysis.

Factor Extraction

Two main methods are used to decide upon the number of emerging factors, Kaiser’s criterion for those factors with an eigenvalue of >1 and the screen test. An eigenvalue is an estimate of variance explained by a factor in a data set, and a value >1 indicates greater than average variance [13]. A scree test is the graphic representation of this. Figure 1 shows the screen test that demonstrated the four-factor structure from a tool. The number of factors is identified from the break in the slope. If a straight line is fitted along the eigenvalue rubble, the number of domains within the questionnaire is revealed by the number of factors above the line. This latter method includes a degree of subjectivity in its interpretation [16].


Figure 1: Scree test (Jones & Johnston 2003) [16].

With Principal components analysis (PCA), the removal of redundant items within a developing measure occurs within an iterative process. Agius et al. describe an iterative process of removing variables with general loadings (of 0.40 on more than one factor) and weak loadings (failing to load above 0.39 on any factor). This process is applied to the initial unrotated PCA before applying a varimax or oblimin rotation to interpret the structure of the solution [17].


This article emphasizes the need to adopt a logical, systematic and structured approach to tool development. Author presented a framework that supports this type of approach and have illustrated the tool development process using item analysis, factor analytic and related methods and have demonstrated strategies to determine the reliability and validity of the new and developing measure. Here with suggested the need to preplan each stage of the tool development process and provide a series of heuristic strategies to enable the researcher to achieve this.


Select your language of interest to view the total content in your interested language
Post your comment

Share This Article

Recommended Journals

Recommended Conferences

  • 18th World Congress on Clinical Nursing and Practice
    June 11-13, 2018 Athens, Greece
  • 26th Cancer Nursing & Nurse Practitioners Conference
    July 16-17, 2018 London, UK
  • 17th World Congress on Clinical Nursing and Practice
    August 29-30 2018 Zurich, Switzerland
  • 38thAsia-Pacific Nursing and Medicare Summit
    October 03-04, 2018 Osaka, Japan

Article Usage

  • Total views: 12710
  • [From(publication date):
    March-2016 - Mar 21, 2018]
  • Breakdown by view type
  • HTML page views : 12280
  • PDF downloads : 430

Post your comment

captcha   Reload  Can't read the image? click here to refresh

Peer Reviewed Journals
Make the best use of Scientific Research and information from our 700 + peer reviewed, Open Access Journals
International Conferences 2018-19
Meet Inspiring Speakers and Experts at our 3000+ Global Annual Meetings

Contact Us

Agri & Aquaculture Journals

Dr. Krish

[email protected]

1-702-714-7001Extn: 9040

Biochemistry Journals

Datta A

[email protected]

1-702-714-7001Extn: 9037

Business & Management Journals


[email protected]

1-702-714-7001Extn: 9042

Chemistry Journals

Gabriel Shaw

[email protected]

1-702-714-7001Extn: 9040

Clinical Journals

Datta A

[email protected]

1-702-714-7001Extn: 9037

Engineering Journals

James Franklin

[email protected]

1-702-714-7001Extn: 9042

Food & Nutrition Journals

Katie Wilson

[email protected]

1-702-714-7001Extn: 9042

General Science

Andrea Jason

[email protected]

1-702-714-7001Extn: 9043

Genetics & Molecular Biology Journals

Anna Melissa

[email protected]

1-702-714-7001Extn: 9006

Immunology & Microbiology Journals

David Gorantl

[email protected]

1-702-714-7001Extn: 9014

Materials Science Journals

Rachle Green

[email protected]

1-702-714-7001Extn: 9039

Nursing & Health Care Journals

Stephanie Skinner

[email protected]

1-702-714-7001Extn: 9039

Medical Journals

Nimmi Anna

[email protected]

1-702-714-7001Extn: 9038

Neuroscience & Psychology Journals

Nathan T

[email protected]

1-702-714-7001Extn: 9041

Pharmaceutical Sciences Journals

Ann Jose

[email protected]

1-702-714-7001Extn: 9007

Social & Political Science Journals

Steve Harry

[email protected]

1-702-714-7001Extn: 9042

© 2008- 2018 OMICS International - Open Access Publisher. Best viewed in Mozilla Firefox | Google Chrome | Above IE 7.0 version