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Not yet recruitingNCT07541326COMPLHEMATOUpdated Apr 21, 2026

Complementary and Alternative Medicine Among Patients With Hematologic Malignancies in France

An interventional study of Questionnaire on Complementary and Alternative Medicines (CAM) in Hematological Malignancies, sponsored by University Hospital, Limoges. Not yet recruiting at 2 sites in France. Open to participants aged 18 Years and older. Per ClinicalTrials.gov, last updated 2026-04-21.

Sponsored by University Hospital, Limoges · Not applicable, Interventional, and Other

Phase
Not applicable
Study type
Interventional
Enrollment
85
Allocation
Not applicable
Ages
18 Years and older
Sex
All
01

Study summary

Integrative medicine promotes the incorporation of elements from complementary and alternative medicines (CAM) into patient care. These approaches are defined as treatments that are not routinely part of conventional medical care (1). CAM practices include osteopathy, acupuncture, aromatherapy, naturopathy, and various energy-based techniques, although their efficacy is not always well-established. Nevertheless, a meta-analysis on the use of CAM in the context of cancer reported a 40% prevalence of use in 2012 (2). Subsequently, a study conducted in France in 2015 revealed an 83% prevalence of CAM use across all types of cancer, underscoring the interest in these therapies (3). CAM is often employed to alleviate side effects of conventional treatments, such as fatigue, nausea, and vomiting. The 2015 French study primarily focused on solid tumors, with hematological malignancies representing only 2% of the cases, thereby limiting the assessment of CAM use in this context (3). Currently, there is no specific data evaluating the use of CAM among patients with hematological malignancies in France.

Hematological malignancies, unlike solid tumors, are characterized by their diffuse nature, making their localization and treatment more challenging for patients to comprehend (4). Additionally, a qualitative study the investigators conducted on the spiritual needs of patients recently diagnosed with hematological malignancies identified CAM as an area of interest. Among the ten patients in the study, seven were using CAM and reported an improvement in their spiritual well-being, which is defined as the ability to integrate the meaning and purpose of life into their health experiences, through relationships with themselves, others, art, nature, or a higher entity. This aspect of CAM utilization was not explored in our previous study on the spiritual needs of patients, particularly in understanding their appeal and the motivations of patients to adopt them.

Therefore, it appears crucial to explore this practice, which is known to be common among healthcare providers. Understanding these complementary care pathways would enable their safety (e.g., avoiding or informing about potential drug interactions) and foster the patient-provider relationship around a topic that is sometimes considered taboo (5). Ultimately, this would contribute to better supporting patients within a holistic care perspective.

02

Conditions studied

  • Hematological Malignancies

Keywords

  • Alternative medicine
  • complementary medicine
  • blood disease
03

In context

Hematologic Neoplasms

1,444 studies on the registry are indexed under Hematologic Neoplasms; 420 are open to participants now.

This study's planned enrollment of 85 is above the median of 46 across 1,044 interventional studies indexed under Hematologic Neoplasms.

Browse Hematologic Neoplasms studies →

Lead sponsor

University Hospital, Limoges is the lead sponsor of 264 studies on the registry; 38 are open to participants now.

Counted across the registry records on this site, refreshed daily.

04

Who can participate

Ages eligible
18 Years and older
Sexes eligible
All
Accepts healthy volunteers
No

Go through the criteria one by one — yes, no or not sure — and take the list to your doctor or the study team. Kept in this browser only.

Inclusion criteria

  • Patients diagnosed with acute leukemia, lymphoma, or myeloma who are hospitalized and undergoing treatment at any of the study centers, regardless of the stage of the disease.
  • Patients aged 18 years or older.
  • Patients who are literate in French.
  • Patients who have been informed about the study and have provided their consent to participate.
  • Patients covered by health insurance.

Exclusion criteria

Exclusion Criteria:

  • Patients with neurocognitive disorders or severe psychiatric conditions.
  • Patients in the terminal stage of the disease.
  • Patients under legal protection measures, such as guardianship or curatorship.
  • Patients participating in an interventional study on the effectiveness of CAM.
05

Study design

Phase
Not applicable
Primary purpose
Other
Allocation
Not applicable
Intervention model
Single group
Masking
None (open label)
Enrollment
85 participants (estimated)

Study arms

  • Other
    Hematological malignancies (leukemia, lymphoma or myeloma)

    Other: Questionnaire on Complementary and Alternative Medicines (CAM)

Interventions

  • OtherQuestionnaire on Complementary and Alternative Medicines (CAM)

    This study employs a mixed-methods approach, combining quantitative and qualitative methods within a convergent design. Quantitative Data: * Every hospitalized patient will be invited to participate in the quantitative part of the study. * Sociodemographic and disease-related data will be collected. * Participants will complete a questionnaire assessing their use of CAM, created based on existing literature. They will also complete the EORTC QLQ-C30 questionnaire to assess their quality of life and the FACIT-SP questionnaire to evaluate their spiritual well-being, both of which are validated tools for this population. Qualitative Data: * A convenience sampling method will be employed to ensure diversity in participant profiles and to capture a comprehensive range of perspectives. * Semi-structured interviews will be conducted with patients, regardless of whether they use CAM, ensuring coverage of each type of pathology.

06

What researchers measure

Primary outcomes

  1. Proportion of Complementary and alternative Medicine (CAM) use

    This will be determined by identifying patients who report engaging in any form of complementary and alternative medicine, as there is no specific questionnaire available to assess this prevalence

    Time frame: At the end of the study, 18 months after the first inclusion

Secondary outcomes

  1. Percentage of use for each identified CAM

    The frequency of use for each specific CAM therapy identified in our sample will be calculated.

    Time frame: At the end of the study, 18 months after the first inclusion

  2. Themes identified in content analysis:

    Themes will be derived from the content analysis of semi-structured interviews conducted with patients.

    Time frame: At the end of the study, 18 months after the first inclusion

  3. Average specific quality of life score

    The mean score from the European Oraganisation for Research and Treament of Cancer quality of Life Questionnaire Core 30 (EORTC QLQ-C30) questionnaire, validated within our population, will be reported to assess the quality of life of cancer patients. Scores are linearly transformed to a 0-100 scale. For the functional scales and the global health status/quality of life scale, higher scores indicate a better level of functioning or quality of life. In contrast, for the symptom scales/items, higher scores indicate a higher level of symptoms (i.e., worse condition).

    Time frame: At the end of the study, 18 months after the first inclusion

  4. Average score from the Functional Assessment of Chronic Illness Therapy - Spiritual Well-Being (FACIT-Sp) questionnaire

    The mean score from the Functional Assessment of Chronic Illness Therapy - Spiritual Well-Being (FACIT-Sp) questionnaire, validated in our population, will be used to assess the spiritual well-being of patients. The total score of FACIT-Sp ranges from 0 to 156. The higher score indicates a higher level ofspiritual well-being.

    Time frame: At the end of the study, 18 months after the first inclusion

  5. Results of multivariate logistic regression

    The outcomes will include factors associated with CAM use, with variables such as age, gender, spiritual well-being score, and quality of life score being analyzed.

    Time frame: At the end of the study, 18 months after the first inclusion

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Study locations

2 sites
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References and documents

Individual participant data

Plan to share: Undecided

No publications or documents are linked to this record.

09

Timeline

Tracking since Sep 25, 2026
ElapsedEstimatedEstimated, not yet reachedSimilar studies: half by the dot; the band is the middle halfHalf of similar studies reached it by the dot; the band is the middle half, from a quarter to three quarters

Start is estimated for Jun 2026; primary completion for Dec 2027, 18 months later.

Of 185 non-industry interventional studies with no phase under Hematologic Neoplasms, half reached primary completion within 40 months of starting (the median), counting those still running; a quarter within 21 and three quarters within 125. This study's planned 18 months is below that.

Counting every sponsor, half of 191 studies reached it within 40 months; a quarter within 21 and three quarters within 125.

How these figures are worked out, and which studies are left out of them.

Registered
Mar 30, 2026
First posted
Apr 21, 2026
StartEst.
Jun 15, 2026
Primary completionEst.
Dec 15, 2027
CompletionEst.
Dec 15, 2027
Last update
Apr 21, 2026
What these dates mean
Start.
When the first participant enrolled; while estimated, when the study expects to open to recruitment.
Primary completion.
When the last participant was examined or treated to collect data for the study's main question, its primary outcome. A study that stopped early gives the date its data collection stopped.
Completion.
When the last participant's last visit took place, for every outcome, secondary ones and side effects included: the end of the study. Often later than primary completion, sometimes the same day.
Actual and Est.
Actual means the registry says the date has happened. Est. (estimated) is a date the sponsor plans or expects. It can still move, and the sponsor is expected to change it to actual once it has passed.
No changes since tracking began. The registry record was last updated on Apr 21, 2026, before this site started recording changes on Sep 25, 2026. Its history is on ClinicalTrials.gov ↗
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Registry details

Key details

Study ID
NCT07541326
Responsible party
Sponsor
First posted
Apr 21, 2026
Start date
Jun 15, 2026 (estimated)
Primary completion
Dec 15, 2027 (estimated)
Completion
Dec 15, 2027 (estimated)
Last update
Apr 21, 2026

Study contacts

Safirah Akowanou
Contact
safirah.akowanou@chu-limoges.fr
+33555058755
Abdeslam BEN TALEB
Contact
abdeslam.bentaleb@chu-limoges.fr
+33555058616
Jean Toniolo
principal investigator · University Hospital, Limoges

Oversight

Data monitoring committee
No
FDA-regulated drug
No
FDA-regulated device
No
View the source record on ClinicalTrials.gov ↗

Not currently enrolling

This study is not yet recruiting, as verified in Apr 2026. You cannot join it, but the record below documents what was studied.

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