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A pragmatic randomised controlled trial of the effectiveness and cost-effectiveness of screening for osteoporosis in older women for the prevention of fractures

A pragmatic randomised controlled trial of the effectiveness and cost-effectiveness of Screening for Osteoporosis in Older women for the Prevention of fractures (SCOOP)

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
ISRCTN
Registry ID
ISRCTN55814835
Enrollment
11580
Registered
2007-06-19
Start date
2007-02-01
Completion date
Unknown
Last updated
2018-03-19

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Musculoskeletal Diseases: Osteoporosis Musculoskeletal Diseases Osteoporosis

Interventions

Intervention subjects will have a 10-year absolute risk of fracture calculated from a World Health Organization (WHO) risk algorithm based on data from a screening questionnaire and, for some subjects

Sponsors

University of East Anglia (UK)
Lead Sponsor

Eligibility

Sex/Gender
Female

Inclusion criteria

Inclusion criteria: 1. Female 2. Aged 70 to 85 years 3. Able to provide informed consent

Exclusion criteria

Exclusion criteria: 1. Currently known to be on treatment for osteoporosis (other than calcium and vitamin D) 2. Any known co-morbidity that would make entry to the trial inadvisable, in GP's opinion

Design outcomes

Primary

MeasureTime frame
All osteoporosis-related fractures (excluding those of hands, feet, nose and skull), assessed at the annual follow-up visits for 5 years post randomisation.

Secondary

MeasureTime frame
1. All clinical fractures (including hip fractures) 2. Quality of life, assessed by the European Quality of life (EQ-5D) and Short Form 12 (SF-12) questionnaires at baseline (immediately prior to randomisation), 6 and 12 months and then annually for 5 years post randomisation 3. Psychological anxiety, assessed by the State-Trait Anxiety Index at baseline, 6 and 12 months and then annually for 5 years post randomisation 4. Mortality (assessed annually for 5 years post randomisation) A process measure will be treatment adherence as ascertained by an ad-hoc questionnaire at follow-up visits.

Countries

United Kingdom

Outcome results

None listed

Source: ISRCTN (via WHO ICTRP) · Data processed: Feb 4, 2026