Health Psychology Flashcards

1
Q

What did pengpid 2013 do

A

Screening and brief interviews for hazardous and harmful alcohol use among hospital outpatients in south Africa
Results from randomised control trial

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2
Q

What are 3 strengths of pengpid 2013

A
  1. Generalisability - longitudinal study as it was carried out for 12 months meaning pps dropped out. 392 pps in baseline down to 282 in 12 month follow up. Therefore 70% still returned after 12 months meaning it isn’t biased in terms of its generalisably

2.reliability - DV measurements were kept standardised, Use of AUDIT test to measure alcohols intake. The health laferlt were kept the same for every pp and the follow up period was the same (6-12 months). Therefore its replicable

  1. Ethics - volunteer sampling was use, outpatients were screened so consent was given. Those with menta
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3
Q

What are 3 weaknesses of pengpid 2013

A
  1. Generalisability - the sample was ethnocentric as there was only 392 adults from South Africa. Therefore lacks population validity as its not generalisable
  2. Attrition - the drop out rate was high over the 12 month period was 29% left by the final AUDIT measurements of alcohol. Therefore sample was less representative
  3. Internal validity - self report method was used by AUDIT test meaning pps can submit inaccurate responses, social desirability. Therefore cause and effect conclusion are not valid
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4
Q

What are randomised control trials

A

One group has therapy whilst the control group doesn’t
They are equal in terms of other characteristics

Pps are randomly allocated to the treatment group or the control group

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5
Q

How are randomised Control trials carried out by

A

Using random computer generators which remove researcher bias so pps have an equal chance of going into either groups

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6
Q

What is placebo

A

A substance or a treatment that isn’t the actual treatment being measured but acts like one so pps can’t tell the difference

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7
Q

What are placebo controlled trials

A

One group gets the actual treatment, other group gets placebo treatment
Pps wont be told which group they’re in therefore it’s a single blind trial
So valid measure of effects of drugs

Sometimes researchers know either, double blind trial which prevents researcher bias

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8
Q

What are 2 health methods

A

Randomised control trials

PET scanning

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9
Q

What are 2 strengths of randomised control trials

A
  1. Validity - if the 2 groups are equal and everything is controlled apart from the IV (2 groups - treatment or control) the the valid-cause-and-effect conclusions can be drawn because the effectiveness of the treatment group can be compares to the control group
  2. Validity - using single and double blind techniques can help avoid the placebo effect and reduce he chance of researcher bias, demand characteristics which improves validity
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10
Q

What are 2 weaknesses of randomised control trials

A
  1. Unethical - the treatment group gets the treatment whereas the control doesn’t. So treatment group gets benefits whilst the other is deprived. This can be overcome by placing the control group on the waiting list so they get the treatment at the end of the trial
  2. Validity - pps can improve by what they perceive to be treatment program no matter what the treatment is, this is the placebo effect, this lowers accuracy of measuring ow effective the treatment s compared to the control list
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11
Q

What does a PET scan involve

A

A radioactive tracer that is injected into the body which is added to a glucose solution that gets used up in the parts of the brain where there is activity

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12
Q

What does the radioactive tracer do

A

Breaks down and produces positively charged positrons

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13
Q

What colour does the hot spots show up as on the scanner

A

Red and orange

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14
Q

What is one biological treatment for nicotine

A

Nicotine replacement therapy

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15
Q

What is the aim of nicotine replacement therapy

A

Bind to receptors at synapses to influence neurotransmission

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16
Q

How does nicotine replacement therapy work

A
  1. Inhaler / patch / gum
  2. Delivers a clean and controlled dose of nicotine without smoking
  3. Binds to acetylcholine receptors in mesolimbic pathway which stimulates dopamine release in NA
  4. Reduce over time stabilises addict
17
Q

What are 2 strengths of nicotine replacement therapy

A
  1. Wide range of ways to take nicotine. Gum, patch, inhaler.
  2. Very accessible for ppl, doesn’t require therapists or professionals, empowering control treatment
18
Q

What are 2 weaknesses of nicotine replacement therapy

A
  1. Side effects - headaches, dizziness and skin irritation due to patches
  2. Replacing the cigarette with nicotine meaning you’re still consuming the substance
19
Q

What is one non biological treatment for nicotine

A

Aversion therapy

20
Q

What is the aim of nicotine aversion therapy

A

To reduce cravings for desired substance

21
Q

How does Nicotine aversion therapy work

A

Aversive stimuli (UCS) = rapid smoking = client takes puff of cigarette (NS) every 6 seconds in a closed room until they finish a set amount or feel sick (UCR)

Repeat process over several session

22
Q

What are 2 strengths of nicotine aversion therapy

A
  1. Ethical - consent, made aware of aim
  2. Not replacing substance with another (NRT) learning new association= long term effect
23
Q

What are 2 weaknesses of nicotine aversion therapy

A
  1. There is commitment, time, effort to attend sessions so pps need to be motivated and willing
  2. High drop out rates before the programme is finished meaning less effective
24
Q

A01 of nicotine aversion therapy

A

Learning new associations
Short term therapy effective up to 1 year
Long term therapy effective up to over 1 year

Stops cravings up to 1-3 months
Not on NHS, private