Trial · NCT07740967
Dietary Supplements and Middle Aged Women (Collagen & Omega)
NCT07740967, Not applicable, Recruiting, Loughborough University
3 sourcestrials-2026-11-12-0.4.0
Cite this record
ConductScience Library. Dietary Supplements and Middle Aged Women (Collagen & Omega). Trials, record NCT07740967. Release trials-2026-11-12-0.4.0, 12 Nov 2026. https://conductscience.org/library/trials/NCT07740967
On this page
Trial
As registered on ClinicalTrials.gov, in the graph's capture of the registry.
- Title
- Dietary Supplements and Middle Aged Women (Collagen & Omega)
- NCT number
- NCT07740967
- Status
- Recruiting
- Phases
- Not applicable
- Enrollment
- 34 participants, estimated
- Lead sponsor
- Loughborough University
- Conditions
Cognition, Inflammation Biomarkers, Bone Metabolism Biomarkers, Fatigue Symptom, Sleep, Body Composition Changes, Joint Pain, Quality of Life, Gastrointestinal Comfort, Blood Pressure and Augmentation Index, Muscle Strength, Fatty Acid Blood Profile
- Interventions
- Collagen peptides and omega-3, Placebo control
- First posted
- 2026-08-03
- Last updated
- 2026-08-03
Source ClinicalTrials.gov
Registered outcomes23
Each outcome the trial registered, primary first, in ClinicalTrials.gov's words.
| List | Outcome | Time frame | Description |
|---|---|---|---|
| Primary | Joint pain under 3 conditions as measured by a 100 mm visual analogue scale (VAS) | 8 weeks | Participants will place a vertical line on the VAS (ranging from no pain (0 mm) to unbearable pain (100 mm)) which will be measured and recorded. Participants will complete a separate VAS for each of the 3 conditions: after standing rest, after 5 body weight squats, and in response to pain levels during daily activities in the last week (such as walking, getting up from chairs, exercising). |
| Secondary | Hand grip strength dynamometry (kg) | 8 weeks | Hand grip strength will be assessed following the Southampton Protocol, where 3 measures will be taken for each hand. |
| Secondary | Blood pressure (mmHg) | 8 weeks | After 10 minutes of seated rest, 3 blood pressure readings will be taken and recorded using an automated cuff. |
| Secondary | Fatigue under 2 conditions measured by a 100 mm visual analogue scale (VAS) | 8 weeks | Participants will place a vertical line on the scale (ranging from no fatigue at all (0 mm) to extremely fatigued (100 mm)) which will be measured and recorded. Participants will complete a visual analogue scale for 2 conditions: right now, and during daily activities in the last week (such as walking, getting up from chairs, exercising). |
| Secondary | Sleep quality measured by an Athens Insomnia Scale | 8 weeks | The Athens Insomnia Scale is an 8-point questionnaire where participants rank different aspects of their sleep (sleep induction, awakenings during the night, final awakening, total sleep duration, overall sleep quality, sense of wellbeing during the day, functioning during the day, and sleepiness during the day) provided that it occurred at least 3 times in the last week from 0 (no issue) to 3 (serious issue). A lower total score indicates better sleep. |
| Secondary | Simple Sleep Quality Scale | 8 weeks | The simple Sleep Quality Scale asks the following question 'During the past 7 days, how would you rate your sleep quality overall?'. Participants select a number from 0 (terrible) to 10 (excellent). A lower score indicates better sleep. |
| Secondary | Aortic Augmentation (AP, mmHg) | 8 weeks | Measured using radial artery tonometry |
| Secondary | Aortic Augmentation Index (AP/PP, %) | 8 weeks | Measured using radial artery tonometry |
| Secondary | Letter Comparison test of cognitive function | 8 weeks | Measuring reaction time (ms) and accuracy (%) |
| Secondary | Backwards Digit Span test of cognitive function | 8 weeks | Measuring the longest correct span score (higher score = better working memory) |
1 to 10 of 23Source ClinicalTrials.gov
See all 23 registered outcomesOutcomes0
Each outcome the trial posted results for, in ClinicalTrials.gov's words.
None in this release.
Results by group0
Each measurement the trial posted, group by group, in the words and numbers it posted.
None in this release.
Participant flow0
How many started, completed or left each group, period by period.
None in this release.
Adverse events0
Each adverse event the trial posted, group by group: the participants affected out of those at risk.
None in this release.
Adverse event totals0
The totals the trial posted for each group.
None in this release.
Papers0
The papers the trial lists on ClinicalTrials.gov.
None in this release.
Grants0
The grants NIH RePORTER links to the trial, newest funded first: NIH's, and some of AHRQ's, CDC's, FDA's and VA's. Each shows its title, principal investigators, organization and funder in its newest year.
None in this release.
Trial comparisons0
Comparisons of the trial's two groups, calculated by ConductScience from the counts it posted.
None in this release.
Tests3
The ConductCognition tests this trial's registered outcomes name, as ScienceGraph matched them in trial-tests-2026-11-12-0.2.1.
| Test | Named as | Source |
|---|---|---|
| Digit Span Test | Secondary outcome | ConductCognition |
| Pattern and Letter Comparison | Secondary outcome | ConductCognition |
| Stroop Color-Word Test | Secondary outcome | ConductCognition |
Source
- Release
- trials-2026-11-12-0.4.0
- Release manifest SHA-256
- 0f4a8d8c48aee2a7573ae0fa94ecbeab70c1adbe449bbc95c424bc7d3e97b9d4
- Registry capture
- 2026-11-12
- Results copy, AACT
- 2026-03-23
- NIH clinical studies file
- 2026-11-13
Source ClinicalTrials.gov
Sources 3
- ClinicalTrials.gov's posted results, through CTTI's AACTFreely available. Acknowledgement requested
- ClinicalTrials.govNone stated
- NIH RePORTER's clinical studies and project filesPublic domain
Each source's terms
- ClinicalTrials.gov's posted results, through CTTI's AACTClinicalTrials.gov data via Aggregate Analysis of ClinicalTrials.gov (AACT), CTTI. CTTI makes its materials freely available and requests acknowledgement. https://aact.ctti-clinicaltrials.org/documentation/299
- ClinicalTrials.govnone stated
- NIH RePORTER's clinical studies and project filesPublic domain (NIH RePORTER)
ClinicalTrials.gov's data carry an international copyright outside the United States: https://clinicaltrials.gov/about-site/terms-conditions.
For software
Read this trial from software.
The record and each of its lists are JSON, twenty rows a page. No key.
GET https://conductscience.org/api/trials/v1/NCT07740967
GET https://conductscience.org/api/trials/v1/NCT07740967/registered?page=2