Trial · NCT07889258
Effects of Wellness Coaching on Quality of Life and Wellness in Oncology Nurses
NCT07889258, Not applicable, Not yet recruiting, Saglik Bilimleri Universitesi
3 sourcestrials-2026-11-12-0.5.0
Cite this record
ConductScience Library. Effects of Wellness Coaching on Quality of Life and Wellness in Oncology Nurses. Trials, record NCT07889258. Release trials-2026-11-12-0.5.0, 12 Nov 2026. https://conductscience.org/library/trials/NCT07889258
On this page
Trial
As registered on ClinicalTrials.gov, in the graph's capture of the registry.
- Title
- Effects of Wellness Coaching on Quality of Life and Wellness in Oncology Nurses
- NCT number
- NCT07889258
- Status
- Not yet recruiting
- Phases
- Not applicable
- Enrollment
- 44 participants, estimated
- Lead sponsor
- Saglik Bilimleri Universitesi
- Conditions
- Quality of Life, Wellness
- Interventions
- Individual Wellness Coaching
- First posted
- 2026-10-22
- Last updated
- 2026-10-22
Source ClinicalTrials.gov
Registered outcomes4
Each outcome the trial registered, primary first, in ClinicalTrials.gov's words.
| List | Outcome | Time frame | Description |
|---|---|---|---|
| Primary | Change From Baseline in Professional Quality of Life: Compassion Satisfaction Subscale Score | Baseline, immediately after the 8-week intervention, and 1 and 3 months after intervention completion. | Compassion satisfaction will be assessed using the Turkish Professional Quality of Life Scale, Version IV (ProQOL-IV). The Compassion Satisfaction subscale contains 10 items rated from 0 to 5. Item scores are summed to obtain a subscale score ranging from 0 to 50. Higher scores indicate greater compassion satisfaction. Change will be calculated by subtracting the baseline score from the score at each subsequent assessment. |
| Primary | Change From Baseline in Professional Quality of Life: Burnout Subscale Score | Baseline, immediately after the 8-week intervention, and 1 and 3 months after intervention completion. | Burnout will be assessed using the Turkish Professional Quality of Life Scale, Version IV (ProQOL-IV). The Burnout subscale contains 10 items rated from 0 to 5. After reverse scoring the designated items according to the instrument's scoring instructions, item scores are summed to obtain a subscale score ranging from 0 to 50. Higher scores indicate greater burnout. Change will be calculated by subtracting the baseline score from the score at each subsequent assessment. |
| Primary | Change From Baseline in Professional Quality of Life: Compassion Fatigue/Secondary Traumatic Stress Subscale Score | Baseline, immediately after the 8-week intervention, and 1 and 3 months after intervention completion. | Compassion fatigue/secondary traumatic stress will be assessed using the Turkish Professional Quality of Life Scale, Version IV (ProQOL-IV). This subscale contains 10 items rated from 0 to 5. Item scores are summed to obtain a subscale score ranging from 0 to 50. Higher scores indicate greater compassion fatigue/secondary traumatic stress. Change will be calculated by subtracting the baseline score from the score at each subsequent assessment. |
| Primary | Change From Baseline in Wellness Wheel Total Score | Baseline, immediately after the 8-week intervention, and 1 and 3 months after intervention completion. | Perceived wellness will be assessed using a researcher-developed Wellness Wheel self-assessment form covering eight domains: physical, emotional, social, intellectual, occupational, financial, spiritual, and environmental wellness. Participants rate each domain from 0 (not well at all/no balance) to 10 (excellent balance and satisfaction). Domain scores are summed to obtain a total score ranging from 0 to 80. Higher scores indicate better perceived wellness. Change will be calculated by subtracting the baseline score from the score at each subsequent assessment. |
Source ClinicalTrials.gov
Outcomes0
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.
Papers4
The papers the trial lists on ClinicalTrials.gov.
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.
Tests0
The ConductCognition tests this trial's registered outcomes name, as ScienceGraph matched them in trial-tests-2026-11-12-0.2.1.
None in this release.
Data dates
The day each source was copied for this release.
Sources 3
- ClinicalTrials.gov's posted results, through CTTI's AACTFreely available. Acknowledgement requested
- ClinicalTrials.govNo license 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/NCT07889258
GET https://conductscience.org/api/trials/v1/NCT07889258/registered