psychopathology AO3 Flashcards

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1
Q

(DOA) strength of statistical deviation

A

there is real life application in the diagnosis. all assessments of patients with mental disorders include measurement of how severe the symptoms are. therefore useful as part of clinical assessment

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2
Q

(DOA) limitation of statistical deviation

A

net help distinguish between desirable and undesirable behaviour. some abnormal behaviour is desirable. using this method alone wouldn’t inform clinic if treatment was needed. reduces usefulness as a measure of classification.

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3
Q

(DOA) strength of deviation from social norms

A

distinguishes between desirable and undesirable behaviour. also takes into account the effect that the behaviour has on others. high validity

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4
Q

(DOA) limitation of deviation from social norms

A

doesn’t consider cultural relativism. the DSM is based on western social norms and ignores Eastern deeming them abnormal. therefore can’t be used as a universal explanation of abnormality.

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5
Q

(DOA) strength of failure to function adequately

A

takes into account individual experiences of the patient. allows us to view mental disorder from the pov of the person. easy to judge objectively. therefore, treatment can be specific to patients needs.

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6
Q

(DOA) limitation of failure to function adequately

A

hard to judge unconventional behaviour. ppt may feel like they are coping just fine. weakness is that it depends who is judging.

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7
Q

(DOA) strength of deviation from ideal mental health

A

focuses on positives over negatives. also focuses on desirable over undesirable behaviour. therefore can be argued it takes more of a positive approach to defining abnormality.

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8
Q

(DOA) limitation of deviation from ideal mental health

A

sets high standards for mental health. hard to generalise. also hard to measure. could be argued this definition is not useable as it is too hard to achieve.

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9
Q

(BATEP) strength of behavioural approach to explaining phobias

A

supportive empirical evidence. Watson and Rayner (1920) used classical conditioning and created phobia in Little Albert. used white rat + loud noise and made a phobia. shows phobias are learnt as little Albert had no phobia before. shows phobias aren’t innate.

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10
Q

(BATEP) limitation of behavioural approach to explaining phobias (not complete explanation)

A

not complete explanation. Bounton (2007) highlights evolutionary factors could play a role in phobias especially if stimulus could’ve caused pain or death. phobia is innate and is a defence mechanism. BATEP does not explain those phobias that are innate

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11
Q

(BATEP) limitation of behavioural approach to explaining phobias (cognitions)

A

ignores role of cognitions. cognitivists argue phobias develop as result of irrational thinking which doesn’t take into account of behaviourists explanation. Cognitive behavioural therapy is more successful treatment which challenges other theories challenging the validity.

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12
Q

(CATED) limitation of cognitive approach to explaining depression (reductionist)

A

too reductionist. states negative thinking develops depression and ignores biological research. therefore cognitive approach too simplistic

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13
Q

(CATED) limitation of cognitive approach to explaining depression (situational factors)

A

ignores situational factors like family problems or life events. these aren’t considered with this explanation

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14
Q

(CATED) strength of cognitive approach to explaining depression (emp evidence)

A

faulty cognitions linked to depression. Grazioli and Terry (2000) studied 65 pregnant women. women judged higher cognitive vulnerability and more likely end with depression. supports cognitive thinking leads to depression. increases validity.

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15
Q

(CATED) strength of cognitive approach to explaining depression (application to real life)

A

app to real life in therapeutic setting. CBT effective treatment for depression. Gautam (2020). faulty thinking responsible for symptoms of depression. this increases validity as cause of depression.

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16
Q

(BATEOCD) (GE) strength of genetic explanation to explaining OCD

A

There is empirical evidence. Nestadt et al (2010) reviewed twin studies. 68% identical shared OCD. Only 31% non identical. Identical twins with 100% shared DNA more likely to develop OCD than twins with only 50% shared DNA. Therefore validity of theory increased however as results are not 100% other factors must be involved.

17
Q

(BATEOCD) (GE) limitation to genetic explanation for explaining phobias (candidate genes)

A

Too many candidate genes (possibly 230). Each genetic variation only increases the risk by a fraction. Limits usefulness as it is too complex meaning there is very low predictive validity. Complexity of genetic variation is a limitation for application to the real world.

18
Q

(BATEOCD) (GE) limitation of genetic explanation for explaining OCD (environmental factors)

A

Ignores environmental factors which play a role. Cromer et al (2007) found over half of OCD sufferes experienced past trauma. OCD more severe the more trauma experienced. Suggests it’s not just genetics causing OCD. Therefore genetic variation is too reductionist and the diathesis stress model is better as it considers genetic and environmental.

19
Q

(BATEOCD) (NE) strength of neural explanations of OCD. (neurotransmitter explanation)

A

Emp evidence does play a role. Antidepressants work system and some antidepressants purely on serotonin. Increase levels of neurotransmitter by blocking the serotonin reuptake process. Drugs are effective at reducing OCD symptoms suggesting serotonin plays a factor. Evidence is correlational and therefore we can’t establish causation.

20
Q

(BATEOCD) (NE) strength of OFC in having a role in OCD (neural explanation)

A

Supportive emp evidence. Menzies et al (2007) used MRI to produce brain activity in OCD sufferers and their immediate family members without OCD and then also a control group. Found OCD sufferers and family members had reduced grey matter in the key regions of the brain. Supports both explanations. Real world application

21
Q

(BATTOCD) Limitation of biological approach to treating OCD. (SSRI + SNRI)

A

Unpleasant side effects. SSRI - indigestion, blurred vision, loss of sex drive. Clomipranine SNRI such as erectile dysfunction, tremors and weight gain. Ashton (1997) used no longer than 4 weeks due to side effects. Not long term.

22
Q

(BATTOCD) strength of biological approach to treating OCD (cost effective)

A

Cost effective. Less disruptive than therapy. Better for NHS, reduces financial pressure. Less disruptive. 1 tablet a day is easier than weekly sessions and doing homework for CBT. Preferred treatment.

23
Q

(BATTOCD) Strength of biological approach to treating OCD (emp evidence)

A

Soomro et al (2009) reviewed studies comparing SSRIs to placebos in treatment of OCD. All 17 studies showed much better results in short term for SSRI. 70% improved treatments. However only 3-4 months long

24
Q

(BATTOCD) limitation of biological approach to treating OCD (publication bias)

A

Concern of publication bias. Turner (2008) claims evidence to show publication bias in more studies t be more effective. Drug companies sponsor research into effectiveness and many companies don’t publish all results. Not all outcomes published - biased evidence.

25
Q

(BATEOCD) (NE) strength of neural explanation of OCD (neural explanation)

A

supportive emp evidence of orbits frontal cortex having role in OCD. Menzies et al (2007) used MRI to produce brain activity in OCD sufferers and their immediate family members without OCD and then also a control group. Found OCD sufferers and family members had reduced grey matter in the key regions of the brain. supports both explanations and has real world application.