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A televised, web-based randomised trial of an herbal remedy (valerian) for insomnia

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
ISRCTN
Registry ID
ISRCTN72748991
Enrollment
550
Registered
2007-03-01
Start date
2007-01-29
Completion date
Unknown
Last updated
2015-01-13

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

Conditions

Primary insomnia Signs and Symptoms Insomnia

Interventions

Coated Valerian Forte tablets 200 mg extract per tablet, corresponding to 1200 mg Valeriana officinalis. 3 tablets to be taken every night for 14 days Information about the study will be televised na

Sponsors

Norwegian Knowledge Centre for the Health Services (Norway)
Lead Sponsor

Eligibility

Inclusion criteria

Inclusion criteria: 1. Aged 18 ?75 years, both inclusive 2. Insomnia lasting more than one month 3. Pittsburgh Sleep Quality Index (PSQI) score of > 5 4. Provide name of primary physician 5. Access to internet and own email address 6. At least 10 days of the sleep diary completed prior to randomisation

Exclusion criteria

Exclusion criteria: 1. Secondary insomnia 2. Use of hypnotics by prescription 3. Depression 4. Alcohol or drug abuse 5. Psychotherapy within the past six months 6. Sleep apnoea, periodic limb movements disorder or restless legs syndrome 7. Pregnant or lactating women or women of childbearing potential who do not use an approved method of contraception (oral contraceptives orIntrauterine device [IUD]) 8. Shift workers 9. History of hypersensitivity to valerian or its constituents 10. Participant rating of ?usually? or ?always? to the following questions in the Global Sleep Assessment Questionnaire: During the past four weeks, how often: a. Did you hold your breath, have breathing pauses, or stop breathing in your sleep? b. Did you have restless or "crawling" feelings in your legs at night that went away if you moved your legs? c. Did you have repeated rhythmic leg jerks or leg twitches during your sleep? d. Did you have nightmares, or did you scream, walk, punch, or kick in your sleep? e. Did any of the following disturb you in your sleep: f. Pain? g. Other physical symptoms? h. Medications? i. Did you snore loudly? 11. Current participation in another trial using an investigational compound

Design outcomes

Primary

MeasureTime frame
Proportion of participants in each group with an improvement in self-assessed quality of sleep of > or = 0.5 units between the average score for the 2 weeks before and 2 weeks during treatment

Secondary

MeasureTime frame
1. Proportion of participants in each group with an improvement of > or = 0.5 units between the average score for the 2 weeks before and 2 weeks during treatment for each of the four variables: 1.1 Sleep latency 1.2 Number of awakenings 1.3 Total sleep time 1.4 Energy level during the day 2. Mean changes in the five outcomes listed above 3. Global self-assessment If a difference is not found between the treatment groups for the primary and secondary variables, the following explorative variables will be analysed: 1. Proportion of participants in each group with any improvement in mean difference (i.e. all score changes > 0) between the average score for the 2 weeks before and 2 weeks during treatment for each of the five variables: 1.1 Quality of sleep 1.2 Sleep latency 1.3 Number of awakenings 1.4 Total sleep time 1.5 Energy level during the day 2. Difference in the profile of the five endpoints during the intervention period taking into account the baseline period, including a potential time effect

Countries

Norway

Outcome results

None listed

Source: ISRCTN (via WHO ICTRP) · Data processed: Apr 6, 2026