Manual for the

Blood-Injection Symptom Scale (BISS)

and the

State Blood-Injection Symptom Scale (S-BISS)

 Andrew C. Page

Department of Psychology, University of Western Australia

  

INDEX

Collaborators

Introduction

The Blood-Injection Symptom Scale (BISS)

The State Blood-Injection Symptom Scale (S-BISS)

References

 

© Andrew C. Page, 1999. This manual may be copied in an unmodified form by clinicians and researchers for use with their clients and subjects. This is acceptable to the author, who, nevertheless, disclaims any responsibility for the consequences of any such use for this material in clinical practice or research. It is not necessary to write to the author for permission to make individual copies. This permission does not extend to making multiple copies for sale.

 

Collaborators

The BISS was developed in collaboration with Kellie S. Bennett, Owen Carter, Julia Smith, and Kirrily Woodmore

The State BISS was developed in collaboration with Anna Fagence, Ilyana Saat, & Nicole Watts

 

Introduction

The Blood-Injection Symptom Scale (BISS; Page, Bennett, Carter, Smith, & Woodmore, 1997) is a scale that is designed to measure symptoms elicited by blood and injection stimuli. It was originally conceived to complement the existing questionnaires that assessed:

1.     General fears and phobias (e.g., the Fear Questionnaire [FQ; Marks & Mathews, 1979] and the Fear Survey Schedule [FSS; Wolpe & Lang, 1977],

2.     Phobic situations avoided by people with concerns about blood and injections (e.g., the Mutilation Questionnaire [MQ; Klorman, Weerts, Hastings, Melamed, & Lang, 1974] and the Medical Fears Survey (MFS; Kleinknecht, Thorndike, & Walls, 1996).]), and

3.     Phobic responses to situations involving blood, injury, and injections (e.g., the Medical Avoidances Survey [MAS; Kleinknecht et al., 1996]).

It aimed to complement these assessments by measuring the symptoms of fear (see Blood Donation Reaction Inventory [BDRI; Meade, France, & Richardson, 1996]) and faintness that occurred in situations involving blood or injections. The original BISS aimed to assess the symptoms that had occurred in the presence of blood and injections during the one of the worst experiences. Since then, the scale has been adapted for use as a state instrument (see Hepburn & Page, 1999) and we are now in the process of developing a state version of the BISS (i.e., the S-BISS). The S-BISS has larger item set and is sensitive to changes in symptoms.

This manual is an evolving document that is intended to capture the state of development of the instrument at the present time. As the tests are refined and more data become available, we will continue to revise the manual.

The Blood-Injection Symptom Scale (BISS)

For a complete account see Page, et al., (1997).

 

Development

Exploratory factor analysis on an initial 300 subjects identified six factors with eigenvalues greater than one, but examination of the scree plot suggested a three factor solution. Given the greater theoretical coherence of the smaller number of factors suggested by the scree plot, we favoured the three factor solution that explained 42% of scale variance. The labels "faintness," "anxiety," and "tension" seemed to capture the nature of the factors. Four of the original 21 items failed to load substantially on the three primary factors and were omitted. The tripartite factor structure was substantiated in a subsequent confirmatory factor analysis on 300 additional Introductory Psychology students. The three latent variables were intercorrelated. Faintness correlated with anxiety (r = .60) and tension (r = .73), and anxiety and tension were also intercorrelated (r = .80).

The resulting scale is a 17-item scale, with the following items:

 

The Blood-Injection Symptom Scale.

These questions ask about sensations that you may experience in situations involving blood or injections. For each sensation, circle "yes" if you noticed the sensation during one of your worst experiences involving blood or injections and circle "no" if you did not notice the sensation during one of your worst experiences involving blood or injections.

1. Did you have tightness, pain or discomfort in your chest?

No / Yes

2. Were you anxious?

No / Yes

3. Did you have blurred vision?

No / Yes

4. Did you have cold or clammy hands?

No / Yes

5. Were you dizzy or lightheaded?

No / Yes

6. Did you feel faint?

No / Yes

7. Were you fatigued?

No / Yes

8. Did you faint?

No / Yes

9. Did feel unreal?

No / Yes

10. Did your heart pound?

No / Yes

11. Were you particularly irritable?

No / Yes

12. Did you feel nauseous?

No / Yes

13. Did the room spin?

No / Yes

14. Did you sweat?

No / Yes

15. Did your muscles feel tense, sore, or ache?

No / Yes

16. Did you tremble?

No / Yes

17. Did you have trouble walking?

No / Yes

 

Scoring

To score the test, a "No" response is given a score of zero and a "Yes" response a score of one.

 

Normative Information

Table 2 in Page et al. (1997) displays the conversions to T-scores for each of the three BISS subscales, the fear subscale (combining anxiety and tension), and the total scale score (summing across the faintness, anxiety and tension) in the original sample of 605 Introductory Psychology students. Subsequently, additional subjects have completed the questionnaire and their data have been collated with the original sample to generate a larger normative sample, now based on 1,251 Introductory Psychology students. All subjects completed the questionnaire during tutorial classes as part of screening sessions to identify individuals who were suitable for participation in further studies. The normative information is available in three different formats. The data are available as descriptive statistics and percentiles for the total sample of 1,251 individuals, descriptive statistics and percentiles for the 1,251 females, descriptive statistics and percentiles for 1,251 males. The BISS scores did not exhibit any relationship with age in the present sample (r = -.05 between age and the total BISS score) and therefore, the sample was not broken down by age.

Descriptive Statistics for Total Sample (n=1,251; Mean age = 19.1)

Subscale

Mean

SD

SEM

BISS Fainting

2.13

2.48

.07

BISS Anxiety

2.48

1.68

.05

BISS Tension

1.10

1.27

.03

BISS Fear

3.58

2.58

.07

BISS Total

5.71

4.57

.13

 

Cut Points for Percentiles of Total Sample (n=1,251)

Percentile

Faintness

Anxiety

Tension

Fear

Total

10

0

0

0

0

0

20

0

1

0

1

1

30

0

1

0

2

2

40

1

2

0

3

3

50

1

2

1

3

5

60

2

3

1

4

6

70

3

3

2

5

8

80

4

4

2

6

10

90

6

5

3

7

12

 

Descriptive Statistics for Males (n=371; Mean age = 19.6)

Subscale

Mean

SD

SEM

BISS Fainting

1.41

1.98

.11

BISS Anxiety

2.06

1.55

.08

BISS Tension

0.87

1.09

.05

BISS Fear

2.93

2.31

.12

BISS Total

4.36

3.91

.29

 

Cut Points for Percentiles of Males

Percentile

Faintness

Anxiety

Tension

Fear

Total

10

0

0

0

0

0

20

0

1

0

1

1

30

0

1

0

1

2

40

0

1

0

2

2

50

1

2

0

3

3

60

1

2

1

3

4

70

2

3

1

4

5

80

3

3

2

5

7

90

4

4

2

6

11

 

Descriptive Statistics for Females (n=879; Mean age = 18.9)

Subscale

Mean

SD

SEM

BISS Fainting

2.42

2.60

.09

BISS Anxiety

2.65

1.71

.06

BISS Tension

1.19

1.33

.05

BISS Fear

3.84

2.65

.09

BISS Total

6.27

4.71

.61

 

Cut Points for Percentiles of Females

Percentile

Faintness

Anxiety

Tension

Fear

Total

10

0

0

0

0

1

20

0

1

0

1

2

30

0

2

0

2

3

40

1

2

0

3

4

50

2

3

1

4

6

60

2

3

1

4

7

70

4

4

2

5

9

80

5

4

2

6

11

90

7

5

3

8

13

 

In Page et al. (1997) subjects were divided according to gender because females reported more symptoms of anxiety (F (1, 595) = 16.43; p < .001), tension (F (1, 590) = 9.80; p < .01), fear (F (1, 587) = 18.80; p < .001), and faintness (F (1, 598) = 23.03; p < .001) than males. Females reported more symptoms on the total BISS than males (F (1, 586) = 27.82; p < .001). In the larger sample of 1,251 subjects females reported more symptoms of anxiety (F (1, 1226) = 32.20; p < .001), tension (F (1, 1224) = 17.33; p < .01), fear (F (1, 1216) = 32.23; p < .001), and faintness (F (1, 1183) = 42.20; p < .001) than males (all tests were two-tailed). Females reported more symptoms on the total BISS than males (F (1, 1170) = 44.10; p < .001).

Page et al. (1997) reported a reliability analysis (using unit weights to sum subscales) indicated that the internal consistency, indicated by coefficient alphas, were .86 for the total scale score, .85 for the nine-item faintness subscale, .68 for the four-item anxiety subscale, .56 for the four-item tension subscale, and .72 for the eight-item fear subscale (where anxiety and tension were combined). Bivariate correlations revealed that the faintness subscale correlated moderately with the fear subscale (r = .50; p < .01), as well as the anxiety (r = .41; p < .01) and tension (r = .43; p < .01) subscales, which in turn correlated moderately with each other (r = .43; p < .01). In the larger sample of 1,251 subjects the respective relationships were similar. The faintness subscale correlated moderately with the fear subscale (r = .60; p < .01), as well as the anxiety (r = .55; p < .01) and tension (r = .49; p < .01) subscales, which in turn correlated moderately with each other (r = .52; p < .01).

 

Validity

Page et al. (1997) were able to replicate Öst's (1992) finding that people with concerns about injections reported greater fearful symptoms than people with concerns about blood. Further, people with concerns about blood were more likely to report symptoms of faintness. The replication of this pattern of results goes some way to validate the BISS.

Hepburn & Page (1999) modified the BISS into a state instrument and reported some additional psychometric information. They modified the instructions to refer to a discrete time period. The wording was: "These questions ask about sensations that you may experience while watching the slide. For each sensation, circle 'yes'" if you noticed the sensation while you watched the slide and circle 'no' if you did not notice the sensation while you watched the slide." To determine if the modification altered the psychometric properties of the instrument, a group of 91 introductory psychology students were recruited. They examined two colour slides, depicting an arm with an open and bloody wound and an arm receiving an injection. Subjects completed the questionnaire before and after each of the two slides. The slides were presented for two minutes. Slide order was counterbalanced across subjects with a ten-minute inter-trial interval.

The total scale score demonstrated satisfactory internal consistency, with coefficient alphas being higher when reporting about symptoms during the presentation of the slides (a = .71) than in the period before presentation of the slides (a = .61). The stability of scores across a short time interval was estimated by averaging the correlations of the two pre-exposure assessments and the two post-test exposure assessments. The average correlation of the total score was .62, indicating stability in the rank ordering of subjects. The total score was also sensitive to the presence of a blood-injection stimulus. The mean number of symptoms endorsed increased from .86 to 2.12 (F (1,90) = 42.63; h 2 = .32; p < .001) when the slides were presented. The total fear and faintness subscales correlated to a moderate degree (r = .38), indicating that the conceptually distinct subscales were measuring different sets of symptoms. (See Table 1 in Hepburn & Page, 1999 for more detail).

In the subsequent experiment, they found that subjects were exposed to a blood-injury phobic slide for twelve trials (four blocks of three) and listened to narratives designed to elicit images associated with fear, disgust, or anger. Reductions in both fear and faintness occurred in every condition, supporting the sensitivity of the index. Construct validity was supported in part because images of fear increased symptoms of both fear and faintness relative to a control. Images of disgust increased symptoms of faintness but not fear.

 

The State Blood-Injection Symptom Scale (S-BISS)

 

Introduction

The State Blood-Injection Symptom scale (SBISS; Page, Fagence, Saat, & Watts, 1999) is a scale that is designed to measure the immediate reactions and symptoms that are elicited by the exposure to blood, injury, and/or injection stimuli. It was developed to complement the trait BISS by assessing immediate state faintness, anxiety, and tension felt in the presence of blood, injury, and/or injection stimuli as well as assessing severity by the use of a five-point Likert type scale.

Development

The SBISS is a modification of the existing BISS. This was achieved by rewording 16 of the items in the BISS to a state nature, re-trialing previous items trialed in the BISS but which failed to make the final measure, adding additional items after a literature search, and changing the response format from a dichotomous format to a five-point Likert type scale. For example, Item 2 in the BISS – "Were you anxious?" was reworded to "To what extent are you feeling anxious". Item 8 in the BISS ("Did you faint?") could not be reworded into a state measure however Item 6 in the BISS - "Did you feel faint?" was reworded to "To what extent are you feeling faint?". Secondly, 20 items that were previously trialed in the BISS but which failed to make the final BISS were reworded for inclusion into the SBISS. These were reworded into a state format as well as being reworded in other ways. For example, the item "Did you need to go to the toilet?" was reworded into two items for the SBISS – " To what extent are you feeling the urge to urinate?" and "To what extent are you feeling the urge to defecate?". Thirdly, two items were generated by an examination of the blood, injury, and/or injection phobia literature. Fourthly, the dichotomous response format of BISS was changed to a five-point Likert scale to assess severity of the symptoms felt and each item in the SBISS was prefaced with the question – "To what extent are you feeling….?". The anchor points – "not at all", "mildly", "moderately", "strongly", and "severely" were chosen as it was thought that they best represented the experience of feeling the sensation within the individual as well as being relatively similar in their perceived cognitive distance.

Sample

Eighty-five participants (53 female, 32 male) were recruited from the general community (Perth, Western Australia) via advertisement, and conveniently sampled from the University of Western Australia’s introductory psychology course. Ages ranged from 17 – 52 years (Mdn = 19.0 yr., SD = 8.08). It was found that 11.8% of the sample fulfilled the DSM-IV criteria for Blood-Injury-Injection Phobia. Forty-two participants were shown an eight minute mute video of a surgical procedure in which both blood and injections were present (experimental condition). The remaining 43 participants were shown an eight minute mute wildlife video which featured an number of animals in a forest environment (control condition) and the SBISS was administered pre and post video.

Measure

Of the 37 items trialed, 28 were included into the final SBISS on the basis of item distribution and correlation analysis. The SBISS retained the tripartite factor structure observed in the BISS with items loading on the "faintness", "anxiety", and "tension" factors. The SBISS is presented below.

 

The State Blood-Injection Symptom Scale

 

These questions ask about sensations which you may or may not be experiencing right now. It is important that you answer these questions with regard to how you are feeling right now. For each of the questions you will be asked to rate how strongly you are feeling that sensation. There are five levels to choose from.

0

1

2

3

4

Not at all

Mildly

Moderately

Strongly

Severely

 

For example – if the question does not describe in any way the sensation you are feeling the circle the 0. If the question totally describes that way you are feeling then circle the 4.

Please answer every question and remember to answer the questions with regard to how you are feeling right now.

______________________________________________________________________________________________

To what extent are you feeling:

1) tightness, discomfort, or pain in your chest?

0

1

2

3

4

2) anxious?

0

1

2

3

4

3) that your vision is blurry?

0

1

2

3

4

4) that your hands are cold or clammy?

0

1

2

3

4

5) lightheaded or dizzy?

0

1

2

3

4

6) faint?

0

1

2

3

4

7) that you or things around you are unreal?

0

1

2

3

4

8) that your heart is pounding?

0

1

2

3

4

9) more irritable than usual?

0

1

2

3

4

10) nauseous?

0

1

2

3

4

11) like the room is spinning?

0

1

2

3

4

12) that you are sweating?

0

1

2

3

4

13) that your muscles are tense, sore, or achy?

0

1

2

3

4

14) that you are trembling?

0

1

2

3

4

15) that if you stood up you would have trouble walking?

0

1

2

3

4

16) hot flushes?

0

1

2

3

4

17) chills?

0

1

2

3

4

18) that you are short of breath?

0

1

2

3

4

19) that your thoughts are racing?

0

1

2

3

4

20) like you are about to vomit?

0

1

2

3

4

21) like your fingers are tingling?

0

1

2

3

4

22) that you are restless?

0

1

2

3

4

23) that you are having difficulty swallowing?

0

1

2

3

4

24) tired?

0

1

2

3

4

25) muscle weakness?

0

1

2

3

4

26) headachy?

0

1

2

3

4

27) that your hearing is fuzzy?

0

1

2

3

4

28) disgusted?

0

1

2

3

4

 

Scoring

Reliability

The SBISS is observed to be a reliable measure of the immediate reactions elicited by blood, injury, and/or injection stimuli. The SBISS has a high level of internal consistency (a = .94). Each of the subscales are also seen to exhibit good internal consistency (anxiety - a = .86; tension - a = .83; faintness - a = .83). The SBISS appears to be sensitive to change as there was a significant difference between scores on the SBISS pre and post video (t (41) = -2.55; p = .01) in the experimental condition (surgical video).

Validity

Validity was measured by correlating the SBISS with a number of measures that were administered at the same time as the SBISS.

Concurrent validity:

Concurrent validity was measured by correlating scores on the post video administration of the SBISS with scores on the BISS. It was found that there was a positive correlation (r = .47; p < .001) between the scores.

Convergent validity:

Convergent validity was measured by correlating the anxiety and tension subscale scores on the post video administration of the SBISS with the anxiety and stress subscales scores on the post video administration of the Depression Anxiety Stress Scale (DASS; Lovibond & Lovibond, 1995) which was also administered pre and post video. It was found that both the anxiety and tension subscales of the SBISS significantly correlated with the anxiety and stress subscales of the DASS (anxiety-anxiety: r = .76; p < .0001, tension-stress: r = .47; p < .0001).

Discriminant validity:

Discriminant validity was measured by comparing the scores on the depression subscale of the DASS with scores on all three subscales of the SBISS. There were no significant correlations between the subscales (faintness-depression: r = -.003; p = .98, anxiety-depression: r = .01; p = .94, tension-depression: r = .09; p = .42).

Construct validity:

Construct validity was measured by correlating scores on the post video administration SBISS with scores on the Medical Fears Survey (MFS: Kleinknecht, Thorndike, & Walls, 1996) which was administered pre video. It was found that the total score on the SBISS was significantly correlated with the total score on the MFS (r = .56; p < .0001). Additionally, the SBISS’s subscales were found to be significantly correlated with subscales ("injection and blood", and "blood") in the MFS (tension-injections and blood draws: r = .42; p < .0001, tension-blood: r = .38; p < .0001, faintness-blood: r = .47; p < .0001, anxiety-injections and blood draws: r = .46; p < .0001).

References

* Indicates references using the BISS

* Hepburn, T., & Page, A. C. (1999). Effects of images about fear and disgust upon responses to blood-injury phobic stimuli. Behavior Therapy, 30, 63-77.

Kleinknecht, R. A., Thorndike, R. M., & Walls, M. M. (1996). Factorial dimensions and correlates of blood, injury, injection and related medical fears: Cross validation of the Medical Fears Survey. Behaviour Research and Therapy, 34, 323-331.

Klorman, R., Weerts, T., Hastings, J., Melamed, B., & Lang, P. (1974). Psychometric description of some fear-specific questionnaires. Behavior Therapy, 5, 401-409.

Lovibond, P., & Lovibond, S. (1995). The structure of negative emotional states: Comparison of the Depression Anxiety Stress Scale with the Beck Depression and Anxiety Inventories. Behavior, Research, and Therapy, 33, 335-343.

Marks, I. M., & Mathews, A. M. (1979). Brief standard self-rating for phobic patients. Behaviour Research and Therapy, 17, 263-267.

Meade, M. A., France, C. R., & Peterson, L. M. (1996). Predicting vasovagal reactions in volunteer blood donors. Journal of Psychosomatic Research, 40, 495-501.

Öst, L-G. (1992). Blood and injection phobia: Background and cognitive, physiological, and behavioral variables. Journal of Abnormal Psychology, 101, 68-74.

Page, A. C. (1994). Blood-injury phobia. Clinical Psychology Review, 14, 443-461.

* Page, A. C., Bennett, K., Carter, O., Smith, J., & Woodmore, K. (1997). The Blood-Injection Symptom Scale (BISS): Assessing a structure of phobic symptoms elicited by blood and injections. Behaviour Research and Therapy, 35, 457-464.

Wolpe, J., & Lang, P. J. (1977). Manual for the Fear Survey Schedule. San Diego, CA: Educational and Industrial Testing Service.

 

Address: http://www.psy.uwa.edu.au/user/andrew/biss.htm

Email: / andrew@psy.uwa.edu.au

Last Updated: October 13, 2000