Research Proposal Toolkit
Drop-in paragraphs for the parts of a grant, IRB, or pilot protocol that researchers spend disproportionate time writing - data handling, AI disclosure, budget, methods, citation. Copy, adapt, paste. Every claim links to a source legal document; nothing here is novel.

Cite this resource
Walkom, G. (2026). Research Proposal Toolkit (CC BY-SA 4.0). withVR. Retrieved from https://withvr.app/resources/research-proposal-toolkit
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Open in Google Docs to copy and adapt, or download as a PDF.
This toolkit is designed for the moment in proposal-writing when you have least time and the most boilerplate to produce. Every section below is a finished paragraph you can paste into the corresponding part of your application, then adapt to fit your study. For the underlying source documents, see the Compliance page and the legal index.
If you have a grant deadline under 72 hours, email hello@withvr.app with "Urgent grant quote" in the subject line. You will get a same-business-day reply with a quote on letterhead.
1. Methods paragraph (short form, ~80 words)
For the part of the methods section that introduces the platform.
2. Methods paragraph (long form, ~250 words)
For methods sections that need more detail on capability and design.
3. IRB / ethics data-handling paragraph (short form, ~100 words)
For the section of an IRB or ethics application describing how participant data is handled by the platform.
4. IRB / ethics data-handling paragraph (long form, ~250 words)
For protocols that require fuller technical detail.
5. AI involvement disclosure (for ethics protocol or participant information sheet)
For the part of an ethics application or participant information sheet that discloses AI use. Aligns with the EU AI Act Article 50 transparency obligation (in force from 2 August 2026).
6. Budget table (paste into your grant spreadsheet)
Typical research budget lines for a VR-based study using Therapy withVR.
| Line item | Notes |
|---|---|
| Therapy withVR software subscription | €49/month per seat (ex. VAT, when billed annually). Custom research/education pricing on request - multi-year bundles up to 5 years, multiple seats, quotes on letterhead, purchase-order billing supported. |
| Meta Quest 3S headset (×n) | ~$350 USD / ~€350 EUR each. Purchased directly from Meta - withVR does not sell hardware. |
| Silicone face covers (hygiene, shared use) | ~€10 each; plan for one per participant pool cycle. Sold separately by third-party retailers - withVR does not sell hygiene supplies. |
| Research assistant time (setup, training, session running) | Initial setup ~1 hour live training call. Ongoing minimal once trained. |
| Participant compensation, ethics fees, transcription, statistical support | Institution-specific - not part of the Therapy withVR cost. |
7. DPIA helper (GDPR Article 35)
A Data Protection Impact Assessment is required under GDPR Article 35 where processing is "likely to result in a high risk" to data subjects. For most VR-SLT research using Therapy withVR, the platform's architecture (no PHI, no audio/video, no special-category data, EU hosting, AES-256, no AI training on inputs) materially reduces the risk profile. Whether a DPIA is required for your specific study is an institutional determination, but withVR BV provides supporting documentation on request. Typical DPIA-relevant facts about Therapy withVR:
- Data location: Frankfurt, Germany (EU). No personal data stored outside the EEA on withVR BV's own infrastructure.
- Encryption: AES-256 at rest (Google Cloud) and at the application layer (profile names, with unique IVs per record). TLS 1.2+ in transit.
- Categories of personal data processed: participant pseudonym/profile label, session timing, avatar configuration, sentences sent, sounds played, emotions triggered. No audio. No video. No biometric data.
- Data subject rights: access, rectification, erasure, restriction, portability, objection, withdrawal of consent - supported per GDPR Articles 15-22.
- Sub-processors: Google Cloud (EU), Google Text-to-Speech (EU processing terms), OpenAI (US, SCCs), Stripe (US, SCCs + DPF), MailerLite (EU). Full list at withvr.app/sub-processor-list.
- Retention: account/subscription 5 years post-end; session/profile 3 years post-end; research data under Research Agreement 24 months post-project; billing 7 years (Belgian accounting law).
- Breach notification: 72 hours to GBA per GDPR Article 33; institutional Controller notified within 72 hours per DPA.
Request DPIA-supporting documentation from legal@withvr.app.
8. Citation
Suggested citation formats for the platform itself in your publication. As Therapy withVR is regularly updated, including the access date is recommended.
Where a publisher or institution requires attribution for screenshots or visual materials, the suggested attribution is: "Used with permission by https://withvr.app".
9. Pre-registration helper (OSF, AsPredicted, etc.)
Suggested fields specifically for VR-SLT studies, when pre-registering on Open Science Framework, AsPredicted, or similar:
- Platform and version. Therapy withVR v[x.y.z] - check the in-app About screen at session-running time.
- Headset. Specify Meta Quest 2 / 3 / 3S / Pro and the firmware version if known.
- Scenario configuration. Environment, number of avatars, avatar emotions, ambient sound profile, language and voice profile, session duration. (Save the configuration as a profile in the platform; pre-register the profile name.)
- AI features used. List which optional OpenAI features were active (sentence translation, text generation, autocorrect, Whisper, speaker grammar, formality, emotional speech) - or note "none, default-off" if all optional AI features were disabled.
- Operator/researcher interventions. Pre-specify under what conditions the researcher will adjust scene complexity mid-session, pause, or terminate.
- Outcome measures collected outside the platform. List the measurement instruments and where they are stored (institutional REDCap, Qualtrics, etc.).
- Stopping rule for adverse experience. Pre-specify the criteria for terminating a session (e.g., self-reported nausea, fatigue, distress).
10. Before-you-submit checklist
- Ethics committee / IRB has approved the use of AI features in your study (if any are activated).
- Informed consent form discloses AI involvement (synthetic voices; any optional features used) where required by your professional standards or applicable law.
- Participant information sheet reflects what the participant will actually experience (synthetic voices, scenarios used, modalities supported).
- Data Processing Agreement requested from withVR BV (if institutional procurement requires it).
- Sub-processor list reviewed against any institutional procurement restrictions on data transfers.
- Budget includes hardware and face covers (third-party purchases, not part of the withVR subscription).
- Pre-registration includes the platform version and the saved scenario profile name.
- Citation format chosen and access date recorded.
- Researcher trained on the platform (one-hour live onboarding call with withVR BV included with subscription).
Supporting documents available on request
Email legal@withvr.app:
- Research Agreement (template) - defines research-data ownership, publication freedoms, retention.
- Data Processing Agreement (template) - GDPR Article 28 processor obligations.
- VPAT v2.5 (March 2026) - accessibility conformance report (WCAG 2.0/2.1/2.2, Section 508, EN 301 549).
- Business Continuity & Disaster Recovery Summary - service resilience, dependency assessment, recovery objectives.
- Patch Management Policy - vulnerability handling, patch timelines, exception procedures.
- EU AI Act Compliance Statement - classification, Article 50 disclosure, prohibited-practices review.
Want a paragraph adapted to your specific protocol or institution? Email hello@withvr.app with the gap you are filling. Turnaround is usually quick.
Related resources
- CAT One-Pagers - Critically appraised topics for the literature review section.
- Journal Club Packs - Team-based deep reads of specific studies.
- IEP / EHCP Goal-Writing Template - Access and participation goals as outcome measures.
- Goal Rating Sheet - Self-rated outcome data for single-case and small-N designs.
- Informed Consent Template - A starting point for the consent section of the protocol.
- Evidence Hub - Catalog of clinical VR studies, organized by topic and assessment.
- Nudelman et al. 2026 scoping review (AJSLP) - The first peer-reviewed map of immersive VR in the field. A useful single citation in the background or literature-review section of any new protocol.